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<loc>https://chemplayer.com/lab-perfect-truffles-with-marou-chocolate</loc>
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<video:title>'Lab perfect' truffles with Marou chocolate video tutorial + subtitles</video:title>
<video:description> 'Lab perfect' truffles with Marou chocolate video tutorial, with subtitles. easy to follow and learn chemistry for home chemists and enthusiasts! </video:description>
<video:thumbnail_loc>https://chemplayer.com/media/lab-perfect-truffles-with-marou-chocolate.jpg</video:thumbnail_loc>
<video:content_loc>https://chemplayer.com/media/lab-perfect-truffles-with-marou-chocolate.mp4</video:content_loc>
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<url>
<loc>https://chemplayer.com/5-iodovanillin-preparation-from-vanillin</loc>
<video:video>
<video:title>5-Iodovanillin preparation from vanillin</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/5-iodovanillin-preparation-from-vanillin.jpg</video:thumbnail_loc>
<video:description>We then weigh out 7.5 grams of pure vanillin powder. Pure vanillin is available under the RoVanil branded professional bakery suppliers...Prepare 12.6 grams of solid iodine</video:description>
<video:content_loc>https://chemplayer.com/media/5-iodovanillin-preparation-from-vanillin.mp4</video:content_loc>
<video:duration>270.09</video:duration>
<video:rating>3.6</video:rating>
<video:live>no</video:live>
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<url>
<loc>https://chemplayer.com/8-reactions-which-failed-and-music-ep</loc>
<video:video>
<video:title>8 reactions which failed and music EP</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/8-reactions-which-failed-and-music-ep.jpg</video:thumbnail_loc>
<video:description></video:description>
<video:content_loc>https://chemplayer.com/media/8-reactions-which-failed-and-music-ep.mp4</video:content_loc>
<video:duration>900.0</video:duration>
<video:rating>4.8</video:rating>
<video:live>no</video:live>
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<url>
<loc>https://chemplayer.com/a-crazy-way-to-make-liquid-bromine</loc>
<video:video>
<video:title>A crazy way to make liquid bromine!</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/a-crazy-way-to-make-liquid-bromine.jpg</video:thumbnail_loc>
<video:description>We wanted to make some more bromine for some experiments so we ordered some sodium bromide....Well we don't know much about bromates so we did a few experiments to see if we could get the bromine out of them.</video:description>
<video:content_loc>https://chemplayer.com/media/a-crazy-way-to-make-liquid-bromine.mp4</video:content_loc>
<video:duration>435.0</video:duration>
<video:rating>4.5</video:rating>
<video:live>no</video:live>
</video:video>
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<url>
<loc>https://chemplayer.com/acetic-anhydride-from-phosphorus-pentoxide-and-acetic-acid</loc>
<video:video>
<video:title>Acetic anhydride from phosphorus pentoxide and acetic acid</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/acetic-anhydride-from-phosphorus-pentoxide-and-acetic-acid.jpg</video:thumbnail_loc>
<video:description>We had read that it wasn't possible to produce acetic anhydride via the dehydration of acetic...But we wanted to test this so we got a small amount of phosphorus pentoxide in a beaker.</video:description>
<video:content_loc>https://chemplayer.com/media/acetic-anhydride-from-phosphorus-pentoxide-and-acetic-acid.mp4</video:content_loc>
<video:duration>540.26</video:duration>
<video:rating>4.4</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.264Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/acetic-anhydride-from-sodium-acetate-and-nitrogen-dioxide</loc>
<video:video>
<video:title>Acetic anhydride from sodium acetate and nitrogen dioxide</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/acetic-anhydride-from-sodium-acetate-and-nitrogen-dioxide.jpg</video:thumbnail_loc>
<video:description>And don't forget to subscribe for more videos like this one.</video:description>
<video:content_loc>https://chemplayer.com/media/acetic-anhydride-from-sodium-acetate-and-nitrogen-dioxide.mp4</video:content_loc>
<video:duration>636.39</video:duration>
<video:rating>3.6</video:rating>
<video:live>no</video:live>
</video:video>
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<url>
<loc>https://chemplayer.com/acetic-anhydride-preparation-via-the-classic-method</loc>
<video:video>
<video:title>Acetic anhydride preparation via the 'classic' method</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/acetic-anhydride-preparation-via-the-classic-method.jpg</video:thumbnail_loc>
<video:description>We'll be preparing acetic anhydride the...thing in this reaction is that your sodium acetate must be anhydrous and</video:description>
<video:content_loc>https://chemplayer.com/media/acetic-anhydride-preparation-via-the-classic-method.mp4</video:content_loc>
<video:duration>440.0</video:duration>
<video:rating>4.3</video:rating>
<video:live>no</video:live>
</video:video>
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<url>
<loc>https://chemplayer.com/acetic-anhydride-via-acetyl-iodide</loc>
<video:video>
<video:title>Acetic anhydride via acetyl iodide</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/acetic-anhydride-via-acetyl-iodide.jpg</video:thumbnail_loc>
<video:description>You've all heard of acetochloride, and we've made this in a previous video.</video:description>
<video:content_loc>https://chemplayer.com/media/acetic-anhydride-via-acetyl-iodide.mp4</video:content_loc>
<video:duration>770.04</video:duration>
<video:rating>5.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
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</url>
<url>
<loc>https://chemplayer.com/acetonitrile-synthesis-from-acetic-acid-via-acetamide</loc>
<video:video>
<video:title>Acetonitrile synthesis from acetic acid via acetamide</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/acetonitrile-synthesis-from-acetic-acid-via-acetamide.jpg</video:thumbnail_loc>
<video:description>In this video we'll be preparing crude acetamide as shown here, then using this to prepare acetonitrile,</video:description>
<video:content_loc>https://chemplayer.com/media/acetonitrile-synthesis-from-acetic-acid-via-acetamide.mp4</video:content_loc>
<video:duration>591.0</video:duration>
<video:rating>4.5</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
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</url>
<url>
<loc>https://chemplayer.com/acetyl-chloride-preparation-no-chlorinating-agents-needed</loc>
<video:video>
<video:title>Acetyl chloride preparation (no chlorinating agents needed!)</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/acetyl-chloride-preparation-no-chlorinating-agents-needed.jpg</video:thumbnail_loc>
<video:description>We did a test and bubbled HCl gas through a equimolar mixture of acetonitrile and acetic acid at room temperature until no more would dissolve....We assembled an apparatus which would allow us to slowly generate HCl gas and bubble this through the liquid mixture whilst suspended in an ice bath and completely closed to the atmosphere.</video:description>
<video:content_loc>https://chemplayer.com/media/acetyl-chloride-preparation-no-chlorinating-agents-needed.mp4</video:content_loc>
<video:duration>457.18</video:duration>
<video:rating>3.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/acetylanthranilic-acid-and-a-failed-test-for-triboluminescence</loc>
<video:video>
<video:title>Acetylanthranilic acid and a (failed) test for triboluminescence</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/acetylanthranilic-acid-and-a-failed-test-for-triboluminescence.jpg</video:thumbnail_loc>
<video:description>use. You can find out how to make this in our other video linked here. We transferred the...out 25 ml of acetic anhydride. You can find out how to make this in another of our videos linked</video:description>
<video:content_loc>https://chemplayer.com/media/acetylanthranilic-acid-and-a-failed-test-for-triboluminescence.mp4</video:content_loc>
<video:duration>344.05</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/acetylglycine-and-preparing-an-oxazolone-heterocycle</loc>
<video:video>
<video:title>Acetylglycine and preparing an oxazolone heterocycle</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/acetylglycine-and-preparing-an-oxazolone-heterocycle.jpg</video:thumbnail_loc>
<video:description>So this will be a video in two parts....We've covered off how to make this in a few different videos before.</video:description>
<video:content_loc>https://chemplayer.com/media/acetylglycine-and-preparing-an-oxazolone-heterocycle.mp4</video:content_loc>
<video:duration>883.0</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
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</url>
<url>
<loc>https://chemplayer.com/acetylsalicylic-acid-extraction-from-aspirin-tablets</loc>
<video:video>
<video:title>Acetylsalicylic acid extraction from aspirin tablets</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/acetylsalicylic-acid-extraction-from-aspirin-tablets.jpg</video:thumbnail_loc>
<video:description>We were recently given some aspirin as a gift and we have been dreaming up some ideas of what to do with it....Here we go. We're using 48 tablets each containing 500 mg of acetylsalicylic acid.</video:description>
<video:content_loc>https://chemplayer.com/media/acetylsalicylic-acid-extraction-from-aspirin-tablets.mp4</video:content_loc>
<video:duration>272.39</video:duration>
<video:rating>4.4</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
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<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/adipic-acid-via-oxidation-of-cyclohexanone</loc>
<video:video>
<video:title>Adipic acid via oxidation of cyclohexanone</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/adipic-acid-via-oxidation-of-cyclohexanone.jpg</video:thumbnail_loc>
<video:description>Check out our previous video for more details of how we made this starting from cyclohexanol.</video:description>
<video:content_loc>https://chemplayer.com/media/adipic-acid-via-oxidation-of-cyclohexanone.mp4</video:content_loc>
<video:duration>599.31</video:duration>
<video:rating>4.5</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
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<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/alkaline-hydrolysis-of-methyl-salicylate</loc>
<video:video>
<video:title>Alkaline hydrolysis of methyl salicylate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/alkaline-hydrolysis-of-methyl-salicylate.jpg</video:thumbnail_loc>
<video:description>aspirin tablets, but it uses lots of solvent and it's difficult to get a lot of product....Salicylates are useful compounds and luckily there's another very OTC source of these compounds.</video:description>
<video:content_loc>https://chemplayer.com/media/alkaline-hydrolysis-of-methyl-salicylate.mp4</video:content_loc>
<video:duration>879.0</video:duration>
<video:rating>4.1</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/aluminium-amalgam-from-a-broken-thermometer</loc>
<video:video>
<video:title>Aluminium amalgam from a broken thermometer</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/aluminium-amalgam-from-a-broken-thermometer.jpg</video:thumbnail_loc>
<video:description>We recently broke a mercury thermometer....This was unfortunate, but then we realized we could salvage the mercury from it and maybe do something interesting.</video:description>
<video:content_loc>https://chemplayer.com/media/aluminium-amalgam-from-a-broken-thermometer.mp4</video:content_loc>
<video:duration>432.0</video:duration>
<video:rating>4.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
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<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/ammonium-methylsulfate-preparation-from-sulfamic-acid</loc>
<video:video>
<video:title>Ammonium methylsulfate preparation from sulfamic acid</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/ammonium-methylsulfate-preparation-from-sulfamic-acid.jpg</video:thumbnail_loc>
<video:description>to take to either dissolve the sulfamic acid or to drive the reaction to a considerable...This goes into the flask with the sulfamic acid.</video:description>
<video:content_loc>https://chemplayer.com/media/ammonium-methylsulfate-preparation-from-sulfamic-acid.mp4</video:content_loc>
<video:duration>614.38</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
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</url>
<url>
<loc>https://chemplayer.com/an-unusual-preparation-of-chloroform</loc>
<video:video>
<video:title>An unusual preparation of chloroform</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/an-unusual-preparation-of-chloroform.jpg</video:thumbnail_loc>
<video:description>They very helpfully shipped us a bottle of trichloroacetic acid....But on reading about trichloroacetic acid, we learned that it's not very stable with</video:description>
<video:content_loc>https://chemplayer.com/media/an-unusual-preparation-of-chloroform.mp4</video:content_loc>
<video:duration>847.23</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
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<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/anhydrous-aluminium-chloride-from-zinc-chloride</loc>
<video:video>
<video:title>Anhydrous aluminium chloride from zinc chloride</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/anhydrous-aluminium-chloride-from-zinc-chloride.jpg</video:thumbnail_loc>
<video:description>There were a few small lumps of zinc chloride,...The residue in the flask looks like gray zinc metal.</video:description>
<video:content_loc>https://chemplayer.com/media/anhydrous-aluminium-chloride-from-zinc-chloride.mp4</video:content_loc>
<video:duration>326.0</video:duration>
<video:rating>4.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/another-7-reactions-which-failed-and-music-ep</loc>
<video:video>
<video:title>Another 7 reactions which failed and music EP</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/another-7-reactions-which-failed-and-music-ep.jpg</video:thumbnail_loc>
<video:description>undefined</video:description>
<video:content_loc>https://chemplayer.com/media/another-7-reactions-which-failed-and-music-ep.mp4</video:content_loc>
<video:duration>889.44</video:duration>
<video:rating>3.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/barbituric-acid-synthesis</loc>
<video:video>
<video:title>Barbituric acid synthesis</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/barbituric-acid-synthesis.jpg</video:thumbnail_loc>
<video:description>151 years ago on this day Adolf von Bayer discovered how to synthesize barbituric acid,...So in honor of the German chemist and to commemorate the day, we're going to synthesize barbituric</video:description>
<video:content_loc>https://chemplayer.com/media/barbituric-acid-synthesis.mp4</video:content_loc>
<video:duration>773.0</video:duration>
<video:rating>4.1</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/benzoin-condensation-the-old-school-way-using-a-cyanide-catalyst</loc>
<video:video>
<video:title>Benzoin condensation the 'old school' way using a cyanide catalyst</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/benzoin-condensation-the-old-school-way-using-a-cyanide-catalyst.jpg</video:thumbnail_loc>
<video:description>We are going to do the classic benzoin condensation reaction....decided to try it the proper old-school way using cyanide as the catalyst.</video:description>
<video:content_loc>https://chemplayer.com/media/benzoin-condensation-the-old-school-way-using-a-cyanide-catalyst.mp4</video:content_loc>
<video:duration>329.1</video:duration>
<video:rating>3.5</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/benzyl-chloride-preparation</loc>
<video:video>
<video:title>Benzyl chloride preparation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/benzyl-chloride-preparation.jpg</video:thumbnail_loc>
<video:description>In this video we'll be preparing benzoyl chloride, a useful synthetic intermediate.</video:description>
<video:content_loc>https://chemplayer.com/media/benzyl-chloride-preparation.mp4</video:content_loc>
<video:duration>703.17</video:duration>
<video:rating>5.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/bio-diesel-from-sunflower-oil</loc>
<video:video>
<video:title>Bio-diesel from sunflower oil</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/bio-diesel-from-sunflower-oil.jpg</video:thumbnail_loc>
<video:description>That's all for this video.</video:description>
<video:content_loc>https://chemplayer.com/media/bio-diesel-from-sunflower-oil.mp4</video:content_loc>
<video:duration>493.0</video:duration>
<video:rating>4.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/bromine-preparation-as-a-solution-in-dcm</loc>
<video:video>
<video:title>Bromine preparation as a solution in DCM</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/bromine-preparation-as-a-solution-in-dcm.jpg</video:thumbnail_loc>
<video:description>We'll demonstrate two different ways to prepare a solution of bromine in dichloromethane,...both using ammonium persulfate as the oxidizing agent.</video:description>
<video:content_loc>https://chemplayer.com/media/bromine-preparation-as-a-solution-in-dcm.mp4</video:content_loc>
<video:duration>633.21</video:duration>
<video:rating>4.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
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<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/can-koh-work-as-a-nitroaldol-catalyst-with-nitroethane</loc>
<video:video>
<video:title>Can KOH work as a nitroaldol catalyst with nitroethane</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/can-koh-work-as-a-nitroaldol-catalyst-with-nitroethane.jpg</video:thumbnail_loc>
<video:description>We made this in our previous video.</video:description>
<video:content_loc>https://chemplayer.com/media/can-koh-work-as-a-nitroaldol-catalyst-with-nitroethane.mp4</video:content_loc>
<video:duration>470.0</video:duration>
<video:rating>4.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/can-aluminium-replace-phosphorus-for-alcohol-reduction</loc>
<video:video>
<video:title>Can aluminium replace phosphorus for alcohol reduction</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/can-aluminium-replace-phosphorus-for-alcohol-reduction.jpg</video:thumbnail_loc>
<video:description>We've tested this in a previous video....this is our last reaction video but we've got a few more interesting things</video:description>
<video:content_loc>https://chemplayer.com/media/can-aluminium-replace-phosphorus-for-alcohol-reduction.mp4</video:content_loc>
<video:duration>865.0</video:duration>
<video:rating>4.1</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/can-thiourea-be-used-to-demethylate-vanillin</loc>
<video:video>
<video:title>Can thiourea be used to demethylate vanillin</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/can-thiourea-be-used-to-demethylate-vanillin.jpg</video:thumbnail_loc>
<video:description>Vanillin demethylation using Fioria....We started with 70 grams of anhydrous zinc chloride and 14 grams of aluminium powder mixed together well as you can see here.</video:description>
<video:content_loc>https://chemplayer.com/media/can-thiourea-be-used-to-demethylate-vanillin.mp4</video:content_loc>
<video:duration>896.0</video:duration>
<video:rating>4.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/carbon-monoxide-preparation-and-how-it-is-deadly</loc>
<video:video>
<video:title>Carbon monoxide preparation, and how it is deadly</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/carbon-monoxide-preparation-and-how-it-is-deadly.jpg</video:thumbnail_loc>
<video:description>Today we're going to experiment and try out a few different procedures for making carbon...Carbon monoxide has the formula CO and it's very different stuff.</video:description>
<video:content_loc>https://chemplayer.com/media/carbon-monoxide-preparation-and-how-it-is-deadly.mp4</video:content_loc>
<video:duration>898.01</video:duration>
<video:rating>3.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/chelidamic-acid</loc>
<video:video>
<video:title>Chelidamic acid</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/chelidamic-acid.jpg</video:thumbnail_loc>
<video:description>You will recall that in the previous video we produced chelotonic acid, the heterocyclic...compound. We're now going to use this to create chelodamic acid, the same compound but with</video:description>
<video:content_loc>https://chemplayer.com/media/chelidamic-acid.mp4</video:content_loc>
<video:duration>378.39</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/chelidonic-acid-synthesis-from-diethyloxalate-and-acetone</loc>
<video:video>
<video:title>Chelidonic acid synthesis from diethyloxalate and acetone</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/chelidonic-acid-synthesis-from-diethyloxalate-and-acetone.jpg</video:thumbnail_loc>
<video:description>We prepared this reagent in a previous video. For more details, click the link shown.</video:description>
<video:content_loc>https://chemplayer.com/media/chelidonic-acid-synthesis-from-diethyloxalate-and-acetone.mp4</video:content_loc>
<video:duration>667.48</video:duration>
<video:rating>4.5</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/chemplayer-guide-to-seduction</loc>
<video:video>
<video:title>ChemPlayer guide to seduction</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/chemplayer-guide-to-seduction.jpg</video:thumbnail_loc>
<video:description>To do this we recommend some brutal medieval samurai carbon steel technology....guess the amine game.</video:description>
<video:content_loc>https://chemplayer.com/media/chemplayer-guide-to-seduction.mp4</video:content_loc>
<video:duration>900.0</video:duration>
<video:rating>4.3</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/chemplayer-tutorials-stoichiometry-and-molar-amounts</loc>
<video:video>
<video:title>ChemPlayer tutorials  - stoichiometry and molar amounts</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/chemplayer-tutorials-stoichiometry-and-molar-amounts.jpg</video:thumbnail_loc>
<video:description>For example like one atom of sulfur and one molecule of oxygen reacting when sulfur burns, forming one molecule of sulfur dioxide gas....Or two molecules of hydrogen and one molecule of oxygen reacting and forming two molecules of water.</video:description>
<video:content_loc>https://chemplayer.com/media/chemplayer-tutorials-stoichiometry-and-molar-amounts.mp4</video:content_loc>
<video:duration>637.06</video:duration>
<video:rating>3.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/chemplayer-tutorials-electrons-part-1</loc>
<video:video>
<video:title>ChemPlayer tutorials - electrons part 1</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/chemplayer-tutorials-electrons-part-1.jpg</video:thumbnail_loc>
<video:description>That's all we're going to cover in this video.</video:description>
<video:content_loc>https://chemplayer.com/media/chemplayer-tutorials-electrons-part-1.mp4</video:content_loc>
<video:duration>900.0</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/chemiluminescence-from-borohydride-and-permanganate-solutions</loc>
<video:video>
<video:title>Chemiluminescence from borohydride and permanganate solutions</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/chemiluminescence-from-borohydride-and-permanganate-solutions.jpg</video:thumbnail_loc>
<video:description>Sodium borohydride is a little hard to obtain for the amateur chemist but we were lucky enough to have a professional donate 400 mg for this video.</video:description>
<video:content_loc>https://chemplayer.com/media/chemiluminescence-from-borohydride-and-permanganate-solutions.mp4</video:content_loc>
<video:duration>193.47</video:duration>
<video:rating>4.5</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/chromium-trioxide-and-pyridinium-chlorochromate</loc>
<video:video>
<video:title>Chromium trioxide and pyridinium chlorochromate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/chromium-trioxide-and-pyridinium-chlorochromate.jpg</video:thumbnail_loc>
<video:description>As it dissolves, the dichromate will cool the solution....This is chromic acid, effectively hydrated chromium trioxide, forming in solution.</video:description>
<video:content_loc>https://chemplayer.com/media/chromium-trioxide-and-pyridinium-chlorochromate.mp4</video:content_loc>
<video:duration>362.3</video:duration>
<video:rating>4.1</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/citrazinic-acid-from-citric-acid-and-urea</loc>
<video:video>
<video:title>Citrazinic acid from citric acid and urea</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/citrazinic-acid-from-citric-acid-and-urea.jpg</video:thumbnail_loc>
<video:description>We will be making citrazenic acid. The yields are not so good but the raw materials are very cheap and easy to come by....Start off with 75 grams of citric acid. Our citric acid claimed to be pure acid but was in fact the monohydrate so try to find out what it is you have.</video:description>
<video:content_loc>https://chemplayer.com/media/citrazinic-acid-from-citric-acid-and-urea.mp4</video:content_loc>
<video:duration>328.42</video:duration>
<video:rating>3.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/clemmensen-reduction-of-vanillin-using-zinc-amalgam</loc>
<video:video>
<video:title>Clemmensen reduction of vanillin using zinc amalgam</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/clemmensen-reduction-of-vanillin-using-zinc-amalgam.jpg</video:thumbnail_loc>
<video:description>Well, we salvaged the mercury and here it is. It's very dense and just this tiny drop weighs nearly half a gram....Last time we used plain nitric acid to dissolve it, but it wasn't so successful.</video:description>
<video:content_loc>https://chemplayer.com/media/clemmensen-reduction-of-vanillin-using-zinc-amalgam.mp4</video:content_loc>
<video:duration>761.31</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/coconut-oil-soap-production-saponification</loc>
<video:video>
<video:title>Coconut oil soap production (saponification)</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/coconut-oil-soap-production-saponification.jpg</video:thumbnail_loc>
<video:description>hydroxide we are going to be using coconut oil as you can see this is a...steamy around here stir the solution well until all the hydroxide dissolves</video:description>
<video:content_loc>https://chemplayer.com/media/coconut-oil-soap-production-saponification.mp4</video:content_loc>
<video:duration>263.0</video:duration>
<video:rating>4.1</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/convert-potassium-ferricyanide-into-ferrocyanide</loc>
<video:video>
<video:title>Convert potassium ferricyanide into ferrocyanide</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/convert-potassium-ferricyanide-into-ferrocyanide.jpg</video:thumbnail_loc>
<video:description>The former contains iron in the plus two oxidation state and the latter in the plus three oxidation state....the first thing we're going to do is show you how to convert it back to the ferrocyanide in a nice clean way.</video:description>
<video:content_loc>https://chemplayer.com/media/convert-potassium-ferricyanide-into-ferrocyanide.mp4</video:content_loc>
<video:duration>444.43</video:duration>
<video:rating>4.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/copper-i-cyanide-preparation</loc>
<video:video>
<video:title>Copper (I) cyanide preparation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/copper-i-cyanide-preparation.jpg</video:thumbnail_loc>
<video:description>So here's the starting material for making cyanide via this method....anhydrous because otherwise the water content with react with the sodium and</video:description>
<video:content_loc>https://chemplayer.com/media/copper-i-cyanide-preparation.mp4</video:content_loc>
<video:duration>874.05</video:duration>
<video:rating>4.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/copper-i-oxide-and-filter-paper-art</loc>
<video:video>
<video:title>Copper (I) oxide and 'Filter Paper Art'</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/copper-i-oxide-and-filter-paper-art.jpg</video:thumbnail_loc>
<video:description>weighed out 6.5 grams of hydroxylamine hydrochloride crystals. This is exotic...and not easily OTC but don't worry we'll be showing you another much easier and</video:description>
<video:content_loc>https://chemplayer.com/media/copper-i-oxide-and-filter-paper-art.mp4</video:content_loc>
<video:duration>897.47</video:duration>
<video:rating>4.4</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/cyanogen-iodide-experimental-preparation</loc>
<video:video>
<video:title>Cyanogen iodide experimental preparation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/cyanogen-iodide-experimental-preparation.jpg</video:thumbnail_loc>
<video:description>was possible to isolate cyanogen iodide without killing ourselves....We figured that if the cyanide was 70% pure, it would be possible to isolate cyanogen iodide</video:description>
<video:content_loc>https://chemplayer.com/media/cyanogen-iodide-experimental-preparation.mp4</video:content_loc>
<video:duration>412.34</video:duration>
<video:rating>3.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/cyclohexanone-oxime</loc>
<video:video>
<video:title>Cyclohexanone oxime</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/cyclohexanone-oxime.jpg</video:thumbnail_loc>
<video:description>Check out our other video for details of how we made this.</video:description>
<video:content_loc>https://chemplayer.com/media/cyclohexanone-oxime.mp4</video:content_loc>
<video:duration>328.0</video:duration>
<video:rating>4.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/cyclohexanone-via-jones-reagent-oxidation</loc>
<video:video>
<video:title>Cyclohexanone via Jones reagent oxidation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/cyclohexanone-via-jones-reagent-oxidation.jpg</video:thumbnail_loc>
<video:description>The reaction works in the 3 to 1 to 8 ratio technically, but we're going to use slightly more dichronate and acid to make sure it goes to completion....Notice that all of the dichronate has now dissolved.</video:description>
<video:content_loc>https://chemplayer.com/media/cyclohexanone-via-jones-reagent-oxidation.mp4</video:content_loc>
<video:duration>677.09</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/cyclohexylamine-via-oxime-reduction-using-zinc-and-acetic-acid</loc>
<video:video>
<video:title>Cyclohexylamine via oxime reduction using zinc and acetic acid</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/cyclohexylamine-via-oxime-reduction-using-zinc-and-acetic-acid.jpg</video:thumbnail_loc>
<video:description>In this video, we're going to try out a different way of reducing N-Otisim to an amine....Check out our previous video for details of how we made this using cyclohexanone and hydroxylamine hydrochloride.</video:description>
<video:content_loc>https://chemplayer.com/media/cyclohexylamine-via-oxime-reduction-using-zinc-and-acetic-acid.mp4</video:content_loc>
<video:duration>535.48</video:duration>
<video:rating>4.1</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/desoxybenzoin-synthesis-2-phenylacetophenone</loc>
<video:video>
<video:title>Desoxybenzoin synthesis (2-phenylacetophenone)</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/desoxybenzoin-synthesis-2-phenylacetophenone.jpg</video:thumbnail_loc>
<video:description>In this video we're going to prepare D6-e-benzoin or 2-phenylacetophenone,</video:description>
<video:content_loc>https://chemplayer.com/media/desoxybenzoin-synthesis-2-phenylacetophenone.mp4</video:content_loc>
<video:duration>436.0</video:duration>
<video:rating>4.2</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/diethyl-oxalate-preparation</loc>
<video:video>
<video:title>Diethyl oxalate preparation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/diethyl-oxalate-preparation.jpg</video:thumbnail_loc>
<video:description>Place the relatively anhydrous oxalic acid into a 500 ml flask....This is almost certainly excess oxalic acid decomposing.</video:description>
<video:content_loc>https://chemplayer.com/media/diethyl-oxalate-preparation.mp4</video:content_loc>
<video:duration>362.0</video:duration>
<video:rating>3.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/diethylmalonate-synthesis-from-chloroacetic-acid</loc>
<video:video>
<video:title>Diethylmalonate synthesis from chloroacetic acid</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/diethylmalonate-synthesis-from-chloroacetic-acid.jpg</video:thumbnail_loc>
<video:description>In this video we'll be preparing diethylmelonate but starting all the way back from chloroacetic...Note we've created this video using clips from various different preparations that</video:description>
<video:content_loc>https://chemplayer.com/media/diethylmalonate-synthesis-from-chloroacetic-acid.mp4</video:content_loc>
<video:duration>865.0</video:duration>
<video:rating>4.4</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/dry-distillation-of-calcium-propionate-and-benzoate</loc>
<video:video>
<video:title>Dry distillation of calcium propionate and benzoate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/dry-distillation-of-calcium-propionate-and-benzoate.jpg</video:thumbnail_loc>
<video:description>Here we will be attempting to prepare propiophenone via the distillation of a mixture of calcium...and propionic acid.</video:description>
<video:content_loc>https://chemplayer.com/media/dry-distillation-of-calcium-propionate-and-benzoate.mp4</video:content_loc>
<video:duration>401.15</video:duration>
<video:rating>4.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/ethyl-chloroacetate-preparation</loc>
<video:video>
<video:title>Ethyl chloroacetate preparation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/ethyl-chloroacetate-preparation.jpg</video:thumbnail_loc>
<video:description>To start we're using the corresponding carboxylic acid that we require, chloroacetic acid, which...We'll add the ethanol to the chloroacetic acid and dissolve it.</video:description>
<video:content_loc>https://chemplayer.com/media/ethyl-chloroacetate-preparation.mp4</video:content_loc>
<video:duration>521.0</video:duration>
<video:rating>4.3</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/ethyl-iodide-using-iodine-and-aluminium-foil</loc>
<video:video>
<video:title>Ethyl iodide using iodine and aluminium foil</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/ethyl-iodide-using-iodine-and-aluminium-foil.jpg</video:thumbnail_loc>
<video:description>In this video we're going to try out an unusual preparation of ethyl iodide.</video:description>
<video:content_loc>https://chemplayer.com/media/ethyl-iodide-using-iodine-and-aluminium-foil.mp4</video:content_loc>
<video:duration>562.0</video:duration>
<video:rating>4.1</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/ethylacetopyruvate-synthesis-from-diethyl-oxalate-and-acetone</loc>
<video:video>
<video:title>Ethylacetopyruvate synthesis from diethyl oxalate and acetone</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/ethylacetopyruvate-synthesis-from-diethyl-oxalate-and-acetone.jpg</video:thumbnail_loc>
<video:description>In this video we'll be synthesizing the compound called ethyl acetopyruvate....Click on the link shown here for our video which demonstrates this.</video:description>
<video:content_loc>https://chemplayer.com/media/ethylacetopyruvate-synthesis-from-diethyl-oxalate-and-acetone.mp4</video:content_loc>
<video:duration>546.0</video:duration>
<video:rating>4.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/experimental-preparation-of-pyridine-n-oxide</loc>
<video:video>
<video:title>Experimental preparation of pyridine-N-oxide</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/experimental-preparation-of-pyridine-n-oxide.jpg</video:thumbnail_loc>
<video:description>In this video we'll prepare pyridine and oxide.</video:description>
<video:content_loc>https://chemplayer.com/media/experimental-preparation-of-pyridine-n-oxide.mp4</video:content_loc>
<video:duration>581.22</video:duration>
<video:rating>3.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/experiments-with-raspberries</loc>
<video:video>
<video:title>Experiments with raspberries</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/experiments-with-raspberries.jpg</video:thumbnail_loc>
<video:description>cooking with chemistry this is the first in a series of two cooking videos we're doing to</video:description>
<video:content_loc>https://chemplayer.com/media/experiments-with-raspberries.mp4</video:content_loc>
<video:duration>900.0</video:duration>
<video:rating>4.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/extract-limonene-and-citrate-from-lemons</loc>
<video:video>
<video:title>Extract limonene and citrate from lemons</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/extract-limonene-and-citrate-from-lemons.jpg</video:thumbnail_loc>
<video:description>Hope you enjoy this video and stay tuned for more soon.</video:description>
<video:content_loc>https://chemplayer.com/media/extract-limonene-and-citrate-from-lemons.mp4</video:content_loc>
<video:duration>898.33</video:duration>
<video:rating>4.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/extraction-of-a-tranquiliser-and-froedhe-s-test</loc>
<video:video>
<video:title>Extraction of a tranquiliser and Froedhe's test</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/extraction-of-a-tranquiliser-and-froedhe-s-test.jpg</video:thumbnail_loc>
<video:description>Benzodiazepine drugs to be invented, and still used in medicine....Well, diazepam isn't that bad.</video:description>
<video:content_loc>https://chemplayer.com/media/extraction-of-a-tranquiliser-and-froedhe-s-test.mp4</video:content_loc>
<video:duration>892.16</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/extreme-grignard-reagents-how-wet-can-you-get</loc>
<video:video>
<video:title>Extreme Grignard reagents -- how wet can you get</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/extreme-grignard-reagents-how-wet-can-you-get.jpg</video:thumbnail_loc>
<video:description>So we attempted to make a Grignard reagent using methyl iodide but using some extreme conditions....While it cooled, our magnesium turnings are from a metal shop.</video:description>
<video:content_loc>https://chemplayer.com/media/extreme-grignard-reagents-how-wet-can-you-get.mp4</video:content_loc>
<video:duration>410.0</video:duration>
<video:rating>3.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/fremy-s-salt-and-a-chemical-mystery</loc>
<video:video>
<video:title>Fremy's salt and a chemical mystery</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/fremy-s-salt-and-a-chemical-mystery.jpg</video:thumbnail_loc>
<video:description>We'll save that for a future video. This is the potassium hydroxylamine disulfonate which we prepared in a previous video....So we've weighed out 1 gram of potassium permanganate crystals.</video:description>
<video:content_loc>https://chemplayer.com/media/fremy-s-salt-and-a-chemical-mystery.mp4</video:content_loc>
<video:duration>588.0</video:duration>
<video:rating>4.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/friedel-crafts-acylation-using-benzene-and-propionic-acid</loc>
<video:video>
<video:title>Friedel-Crafts acylation using benzene and propionic acid</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/friedel-crafts-acylation-using-benzene-and-propionic-acid.jpg</video:thumbnail_loc>
<video:description>You can check out our other video for details of how to make this using zinc chloride.</video:description>
<video:content_loc>https://chemplayer.com/media/friedel-crafts-acylation-using-benzene-and-propionic-acid.mp4</video:content_loc>
<video:duration>438.0</video:duration>
<video:rating>4.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/fuming-nitric-acid-and-nitrogen-pentoxide</loc>
<video:video>
<video:title>Fuming nitric acid and nitrogen pentoxide</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/fuming-nitric-acid-and-nitrogen-pentoxide.jpg</video:thumbnail_loc>
<video:description>We've seen lots of videos on the internet for preparing, fuming nitric acid,...First we start with 35 grams of potassium nitrate.</video:description>
<video:content_loc>https://chemplayer.com/media/fuming-nitric-acid-and-nitrogen-pentoxide.mp4</video:content_loc>
<video:duration>420.19</video:duration>
<video:rating>4.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/ghetto-grignard</loc>
<video:video>
<video:title>Ghetto Grignard</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/ghetto-grignard.jpg</video:thumbnail_loc>
<video:description>grams of cyclohexanone which we prepared in a previous video this is half the</video:description>
<video:content_loc>https://chemplayer.com/media/ghetto-grignard.mp4</video:content_loc>
<video:duration>900.0</video:duration>
<video:rating>3.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/glycine-nitrosyl-chloride-essence-of-smurf</loc>
<video:video>
<video:title>Glycine + Nitrosyl chloride = Essence of Smurf</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/glycine-nitrosyl-chloride-essence-of-smurf.jpg</video:thumbnail_loc>
<video:description>nitrous acid,...Here's a little bit of concentrated 36% hydrochloric acid.</video:description>
<video:content_loc>https://chemplayer.com/media/glycine-nitrosyl-chloride-essence-of-smurf.mp4</video:content_loc>
<video:duration>900.0</video:duration>
<video:rating>4.3</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/glyoxylic-acid-and-experimental-prep-of-hydroxymandelic-acid</loc>
<video:video>
<video:title>Glyoxylic acid and experimental prep of hydroxymandelic acid</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/glyoxylic-acid-and-experimental-prep-of-hydroxymandelic-acid.jpg</video:thumbnail_loc>
<video:description>to prepare a solution of glyoxylic acid then we're going to see if this can...we're starting with 30 grams of oxalic acid dihydrate</video:description>
<video:content_loc>https://chemplayer.com/media/glyoxylic-acid-and-experimental-prep-of-hydroxymandelic-acid.mp4</video:content_loc>
<video:duration>550.06</video:duration>
<video:rating>4.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/henry-condensation-between-vanillin-and-nitroethane-using-a-microwave</loc>
<video:video>
<video:title>Henry condensation between vanillin and nitroethane using a microwave</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/henry-condensation-between-vanillin-and-nitroethane-using-a-microwave.jpg</video:thumbnail_loc>
<video:description>In this video we'll be performing a famous condensation reaction between an...Check out our other video linked here for details about how this can be synthesized.</video:description>
<video:content_loc>https://chemplayer.com/media/henry-condensation-between-vanillin-and-nitroethane-using-a-microwave.mp4</video:content_loc>
<video:duration>438.35</video:duration>
<video:rating>3.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/henry-reaction-between-vanillin-and-nitromethane</loc>
<video:video>
<video:title>Henry reaction between vanillin and nitromethane</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/henry-reaction-between-vanillin-and-nitromethane.jpg</video:thumbnail_loc>
<video:description>now for our nitromethane we prepared this in the previous video so click on...video so we use this to start with this is about a gram of slightly damp slushy</video:description>
<video:content_loc>https://chemplayer.com/media/henry-reaction-between-vanillin-and-nitromethane.mp4</video:content_loc>
<video:duration>644.38</video:duration>
<video:rating>3.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/hydrolysis-of-piracetam-a-nootropic-drug</loc>
<video:video>
<video:title>Hydrolysis of piracetam, a 'nootropic' drug</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/hydrolysis-of-piracetam-a-nootropic-drug.jpg</video:thumbnail_loc>
<video:description>But we'll maybe do this in a future video if we find a use for it.</video:description>
<video:content_loc>https://chemplayer.com/media/hydrolysis-of-piracetam-a-nootropic-drug.mp4</video:content_loc>
<video:duration>814.0</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/hypophosphorus-acid-preparation</loc>
<video:video>
<video:title>Hypophosphorus acid preparation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/hypophosphorus-acid-preparation.jpg</video:thumbnail_loc>
<video:description>we recently acquired an interesting chemical sodium hypophosphate it's the...sodium salt of hypophosphorus acid which can apparently be used together with iodine instead</video:description>
<video:content_loc>https://chemplayer.com/media/hypophosphorus-acid-preparation.mp4</video:content_loc>
<video:duration>452.39</video:duration>
<video:rating>4.5</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/ibuprofen-extraction-and-optical-isomerism</loc>
<video:video>
<video:title>Ibuprofen extraction and optical isomerism</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/ibuprofen-extraction-and-optical-isomerism.jpg</video:thumbnail_loc>
<video:description>tablets today we're going to extract and purify ibuprofen from these and also...milligrams of ibuprofen so that's 16 grams in total</video:description>
<video:content_loc>https://chemplayer.com/media/ibuprofen-extraction-and-optical-isomerism.mp4</video:content_loc>
<video:duration>858.21</video:duration>
<video:rating>3.5</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/iodobenzene-preparation</loc>
<video:video>
<video:title>Iodobenzene preparation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/iodobenzene-preparation.jpg</video:thumbnail_loc>
<video:description>In this camp layer we'll be preparing iodo benzene using a variation on the classic organ....Use ventilation and caution when handling benzene because it seems to act as a trigger</video:description>
<video:content_loc>https://chemplayer.com/media/iodobenzene-preparation.mp4</video:content_loc>
<video:duration>449.17</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-acetyl-chloride-from-acetonitrile</loc>
<video:video>
<video:title>Make acetyl chloride from acetonitrile</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-acetyl-chloride-from-acetonitrile.jpg</video:thumbnail_loc>
<video:description>Then check our other video on how to do this.</video:description>
<video:content_loc>https://chemplayer.com/media/make-acetyl-chloride-from-acetonitrile.mp4</video:content_loc>
<video:duration>814.39</video:duration>
<video:rating>3.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-benzaldehyde-from-benzyl-alcohol-via-persulfate-oxidation</loc>
<video:video>
<video:title>Make benzaldehyde from benzyl alcohol via persulfate oxidation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-benzaldehyde-from-benzyl-alcohol-via-persulfate-oxidation.jpg</video:thumbnail_loc>
<video:description>In this video we'll show you how to produce a decent sized quantity of</video:description>
<video:content_loc>https://chemplayer.com/media/make-benzaldehyde-from-benzyl-alcohol-via-persulfate-oxidation.mp4</video:content_loc>
<video:duration>802.0</video:duration>
<video:rating>4.2</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-dimethyl-oxalate</loc>
<video:video>
<video:title>Make dimethyl oxalate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-dimethyl-oxalate.jpg</video:thumbnail_loc>
<video:description>As we said before, this is useful stuff and we'll be coming back to it in some future videos and also trying it out in some of the preparations we've done in the past with the ethyl esters.</video:description>
<video:content_loc>https://chemplayer.com/media/make-dimethyl-oxalate.mp4</video:content_loc>
<video:duration>676.0</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-hydrazine-using-bleach-and-urea</loc>
<video:video>
<video:title>Make hydrazine using bleach and urea</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-hydrazine-using-bleach-and-urea.jpg</video:thumbnail_loc>
<video:description>By viewer request in this video we're going to prepare hydrazine sulfate starting from household bleach....There are a few other good videos out there which show how to make hydrazine, but none which show this method using urea, and this one does a bit more OTC, although the yields aren't as good.</video:description>
<video:content_loc>https://chemplayer.com/media/make-hydrazine-using-bleach-and-urea.mp4</video:content_loc>
<video:duration>896.34</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-methylamine-hydrochloride</loc>
<video:video>
<video:title>Make methylamine hydrochloride</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-methylamine-hydrochloride.jpg</video:thumbnail_loc>
<video:description>In this video we'll be making methylamine hydrochloride by reacting ammonium chloride and formaldehyde solution....If you liked this video,</video:description>
<video:content_loc>https://chemplayer.com/media/make-methylamine-hydrochloride.mp4</video:content_loc>
<video:duration>484.0</video:duration>
<video:rating>4.3</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-nitrovanillin-via-nitration-of-vanillin</loc>
<video:video>
<video:title>Make nitrovanillin via nitration of vanillin</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-nitrovanillin-via-nitration-of-vanillin.jpg</video:thumbnail_loc>
<video:description>we'd have a go at making one up. Vanillin is a phenol, so the aromatic ring is pretty activated...towards electrophilic attack. So nitration should be pretty easy. With phenol for instance dilute</video:description>
<video:content_loc>https://chemplayer.com/media/make-nitrovanillin-via-nitration-of-vanillin.mp4</video:content_loc>
<video:duration>722.0</video:duration>
<video:rating>4.4</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-p-aminophenol-from-paracetamol</loc>
<video:video>
<video:title>Make p-aminophenol from paracetamol</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-p-aminophenol-from-paracetamol.jpg</video:thumbnail_loc>
<video:description>paracetamol from tablets using an organic solvent such as acetone, ethanol or isopropanol....Acetone is our favorite as it's efficient and easy, and evaporates quickly leaving crystals</video:description>
<video:content_loc>https://chemplayer.com/media/make-p-aminophenol-from-paracetamol.mp4</video:content_loc>
<video:duration>805.0</video:duration>
<video:rating>5.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-piperonal-from-piperinic-acid</loc>
<video:video>
<video:title>Make piperonal from piperinic acid</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-piperonal-from-piperinic-acid.jpg</video:thumbnail_loc>
<video:description>We prepared this in previous videos, starting all the way back from iodine, so go back and...oily component remaining so enjoyed the view from the DCM extract video if you liked this video please subscribe to my channel and hit the bell icon to get notified of future videos</video:description>
<video:content_loc>https://chemplayer.com/media/make-piperonal-from-piperinic-acid.mp4</video:content_loc>
<video:duration>898.0</video:duration>
<video:rating>3.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-potassium-chromate-and-dichromate</loc>
<video:video>
<video:title>Make potassium chromate and dichromate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-potassium-chromate-and-dichromate.jpg</video:thumbnail_loc>
<video:description>Potassium Dichromate Preparation...Potassium Hydroxide</video:description>
<video:content_loc>https://chemplayer.com/media/make-potassium-chromate-and-dichromate.mp4</video:content_loc>
<video:duration>684.0</video:duration>
<video:rating>4.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-potassium-hydroxylamine-disulfonate</loc>
<video:video>
<video:title>Make potassium hydroxylamine disulfonate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-potassium-hydroxylamine-disulfonate.jpg</video:thumbnail_loc>
<video:description>In this video we'll take you on a journey. A journey of failure and woe, but with a positive</video:description>
<video:content_loc>https://chemplayer.com/media/make-potassium-hydroxylamine-disulfonate.mp4</video:content_loc>
<video:duration>893.27</video:duration>
<video:rating>3.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-potassium-perchlorate</loc>
<video:video>
<video:title>Make potassium perchlorate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-potassium-perchlorate.jpg</video:thumbnail_loc>
<video:description>It's worth noting that you can do this reaction using sodium chlorate instead, which may be easier to obtain....We're starting off with 30 grams of potassium chlorate crystals as you can see here.</video:description>
<video:content_loc>https://chemplayer.com/media/make-potassium-perchlorate.mp4</video:content_loc>
<video:duration>682.02</video:duration>
<video:rating>4.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-potassium-permanganate</loc>
<video:video>
<video:title>Make potassium permanganate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-potassium-permanganate.jpg</video:thumbnail_loc>
<video:description>We're going to prepare potassium permanganate starting with manganese dioxide....Prepare the manganese dioxide, which is 35 grams shown here.</video:description>
<video:content_loc>https://chemplayer.com/media/make-potassium-permanganate.mp4</video:content_loc>
<video:duration>581.31</video:duration>
<video:rating>4.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-silver-metal-and-solid-iodine-from-silver-iodide</loc>
<video:video>
<video:title>Make silver metal and solid iodine from silver iodide</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-silver-metal-and-solid-iodine-from-silver-iodide.jpg</video:thumbnail_loc>
<video:description>Check out our previous video for full details of how to make this.</video:description>
<video:content_loc>https://chemplayer.com/media/make-silver-metal-and-solid-iodine-from-silver-iodide.mp4</video:content_loc>
<video:duration>755.0</video:duration>
<video:rating>4.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-sodium-azide-using-hydrazine-sulfate</loc>
<video:video>
<video:title>Make sodium azide using hydrazine sulfate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-sodium-azide-using-hydrazine-sulfate.jpg</video:thumbnail_loc>
<video:description>Check out our previous video for details of how you can make this using urea and sodium</video:description>
<video:content_loc>https://chemplayer.com/media/make-sodium-azide-using-hydrazine-sulfate.mp4</video:content_loc>
<video:duration>899.42</video:duration>
<video:rating>4.3</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-sodium-dithionite</loc>
<video:video>
<video:title>Make sodium dithionite</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-sodium-dithionite.jpg</video:thumbnail_loc>
<video:description>Sovium diphenate is a useful reducing agent in organic synthesis, but unfortunately we...We're starting off with 50 grams of sovium bisulfite which is a fine white powder as</video:description>
<video:content_loc>https://chemplayer.com/media/make-sodium-dithionite.mp4</video:content_loc>
<video:duration>522.38</video:duration>
<video:rating>3.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/make-solid-sodium-ethoxide</loc>
<video:video>
<video:title>Make solid sodium ethoxide</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/make-solid-sodium-ethoxide.jpg</video:thumbnail_loc>
<video:description>As always work quickly with sodium because it tends to rapidly react with atmospheric...Dry the sodium and make sure it's free of mineral oil from storage.</video:description>
<video:content_loc>https://chemplayer.com/media/make-solid-sodium-ethoxide.mp4</video:content_loc>
<video:duration>311.31</video:duration>
<video:rating>4.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/making-urushibara-nickel</loc>
<video:video>
<video:title>Making Urushibara nickel</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/making-urushibara-nickel.jpg</video:thumbnail_loc>
<video:description>Ideally you start off with nickel to chloride crystals, but we don't have those available. Instead we do have basic nickel to carbonate which is a fine green powder as you can see here....What might be useful to remember later is that this contains just over 2.3 grams of nickel metal.</video:description>
<video:content_loc>https://chemplayer.com/media/making-urushibara-nickel.mp4</video:content_loc>
<video:duration>818.0</video:duration>
<video:rating>3.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/malonic-acid-synthesis</loc>
<video:video>
<video:title>Malonic acid synthesis</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/malonic-acid-synthesis.jpg</video:thumbnail_loc>
<video:description>In this video we'll prepare Malonic Acid....We may do a future video on making this, but for this experiment we're using a commercial product.</video:description>
<video:content_loc>https://chemplayer.com/media/malonic-acid-synthesis.mp4</video:content_loc>
<video:duration>854.38</video:duration>
<video:rating>4.3</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/manganese-iii-acetate-preparation</loc>
<video:video>
<video:title>Manganese (III) acetate preparation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/manganese-iii-acetate-preparation.jpg</video:thumbnail_loc>
<video:description>Today we're going to prepare a very unusual compound, manganese 3-acetate which has manganese...And now here's 16 grams of sodium carbonate.</video:description>
<video:content_loc>https://chemplayer.com/media/manganese-iii-acetate-preparation.mp4</video:content_loc>
<video:duration>860.0</video:duration>
<video:rating>4.1</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/manganese-dioxide-and-preparation-of-benzaldehyde-from-benzyl-alcohol</loc>
<video:video>
<video:title>Manganese dioxide and preparation of benzaldehyde from benzyl alcohol</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/manganese-dioxide-and-preparation-of-benzaldehyde-from-benzyl-alcohol.jpg</video:thumbnail_loc>
<video:description>In part 1 of this video we'll prepare what is known as active or chemical</video:description>
<video:content_loc>https://chemplayer.com/media/manganese-dioxide-and-preparation-of-benzaldehyde-from-benzyl-alcohol.mp4</video:content_loc>
<video:duration>715.0</video:duration>
<video:rating>4.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/methyl-iodide-preparation</loc>
<video:video>
<video:title>Methyl iodide preparation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/methyl-iodide-preparation.jpg</video:thumbnail_loc>
<video:description>The first uses methanol with potassium iodide and 85% phosphoric acid....The second is the method we will use which uses the slightly more exotic iodine and red phosphorus.</video:description>
<video:content_loc>https://chemplayer.com/media/methyl-iodide-preparation.mp4</video:content_loc>
<video:duration>327.35</video:duration>
<video:rating>4.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/methyl-iodide-via-the-aluminium-foil-method</loc>
<video:video>
<video:title>Methyl iodide via the 'aluminium foil' method</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/methyl-iodide-via-the-aluminium-foil-method.jpg</video:thumbnail_loc>
<video:description>We've done this experiment before in the previous video where we used iodine and</video:description>
<video:content_loc>https://chemplayer.com/media/methyl-iodide-via-the-aluminium-foil-method.mp4</video:content_loc>
<video:duration>837.0</video:duration>
<video:rating>5.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/methylamine-from-ammonium-methylsulfate</loc>
<video:video>
<video:title>Methylamine from ammonium methylsulfate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/methylamine-from-ammonium-methylsulfate.jpg</video:thumbnail_loc>
<video:description>and a borosilicate glass test tube to do the test scale reaction in....Here's one gram of our ammonium methyl sulfate crushed up into a powder.</video:description>
<video:content_loc>https://chemplayer.com/media/methylamine-from-ammonium-methylsulfate.mp4</video:content_loc>
<video:duration>900.0</video:duration>
<video:rating>4.4</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/methylpropiophenone-synthesis-via-friedel-crafts-acylation</loc>
<video:video>
<video:title>Methylpropiophenone synthesis via Friedel-Crafts acylation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/methylpropiophenone-synthesis-via-friedel-crafts-acylation.jpg</video:thumbnail_loc>
<video:description>You can check out our video for details of how to make this.</video:description>
<video:content_loc>https://chemplayer.com/media/methylpropiophenone-synthesis-via-friedel-crafts-acylation.mp4</video:content_loc>
<video:duration>900.0</video:duration>
<video:rating>4.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/methylpropiophenone-synthesis-via-friedel-crafts-acylation-with-james-earl-jones</loc>
<video:video>
<video:title>Methylpropiophenone synthesis via Friedel-Crafts acylation with James Earl Jones</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/methylpropiophenone-synthesis-via-friedel-crafts-acylation.jpg</video:thumbnail_loc>
<video:description>undefined</video:description>
<video:content_loc>https://chemplayer.com/media/methylpropiophenone-synthesis-via-friedel-crafts-acylation-with-james-earl-jones.mp4</video:content_loc>
<video:duration>900.0</video:duration>
<video:rating>3.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/mono-nitration-of-phenol</loc>
<video:video>
<video:title>Mono-nitration of phenol</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/mono-nitration-of-phenol.jpg</video:thumbnail_loc>
<video:description>We've been wanting to try out the nitration of phenol for a long time,...We won't be making picric acid as it's very dangerous and ultimately not very useful.</video:description>
<video:content_loc>https://chemplayer.com/media/mono-nitration-of-phenol.mp4</video:content_loc>
<video:duration>679.0</video:duration>
<video:rating>4.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/nitroethane-from-ethyl-iodide-and-silver-nitrite-victor-meyer-reaction</loc>
<video:video>
<video:title>Nitroethane from ethyl iodide and silver nitrite ('Victor Meyer reaction')</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/nitroethane-from-ethyl-iodide-and-silver-nitrite-victor-meyer-reaction.jpg</video:thumbnail_loc>
<video:description>The second part is the reaction of this with ethyl iodide to form nitroethane....Badly and potentially burn. Next we weigh out 19 grams of sodium nitrate.</video:description>
<video:content_loc>https://chemplayer.com/media/nitroethane-from-ethyl-iodide-and-silver-nitrite-victor-meyer-reaction.mp4</video:content_loc>
<video:duration>621.23</video:duration>
<video:rating>3.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/nitrogen-triiodide-can-it-convert-aldehyde-to-nitrile</loc>
<video:video>
<video:title>Nitrogen triiodide - can it convert aldehyde to nitrile</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/nitrogen-triiodide-can-it-convert-aldehyde-to-nitrile.jpg</video:thumbnail_loc>
<video:description>video by reducing vanillin there's not enough here to analyze so this might be</video:description>
<video:content_loc>https://chemplayer.com/media/nitrogen-triiodide-can-it-convert-aldehyde-to-nitrile.mp4</video:content_loc>
<video:duration>895.18</video:duration>
<video:rating>3.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/nitromethane-preparation-from-chloroacetic-acid</loc>
<video:video>
<video:title>Nitromethane preparation from chloroacetic acid</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/nitromethane-preparation-from-chloroacetic-acid.jpg</video:thumbnail_loc>
<video:description>Today, we're going to prepare nitromethane via a classic reaction starting from chloroacetic...First, we measured out 45 grams of solid sodium hydroxide into a beaker.</video:description>
<video:content_loc>https://chemplayer.com/media/nitromethane-preparation-from-chloroacetic-acid.mp4</video:content_loc>
<video:duration>786.0</video:duration>
<video:rating>3.5</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/nitrotoluene-from-the-mixed-acid-nitration-of-toluene</loc>
<video:video>
<video:title>Nitrotoluene from the mixed acid nitration of toluene</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/nitrotoluene-from-the-mixed-acid-nitration-of-toluene.jpg</video:thumbnail_loc>
<video:description>listed at the end of this video.</video:description>
<video:content_loc>https://chemplayer.com/media/nitrotoluene-from-the-mixed-acid-nitration-of-toluene.mp4</video:content_loc>
<video:duration>587.0</video:duration>
<video:rating>3.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/nitrourea-preparation-scaled-up</loc>
<video:video>
<video:title>Nitrourea preparation scaled up</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/nitrourea-preparation-scaled-up.jpg</video:thumbnail_loc>
<video:description>previous video and to react with this we've measured out 32 mils of 68%...That's all for this video.</video:description>
<video:content_loc>https://chemplayer.com/media/nitrourea-preparation-scaled-up.mp4</video:content_loc>
<video:duration>743.0</video:duration>
<video:rating>4.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/openchem</loc>
<video:video>
<video:title>OpenChem</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/openchem.jpg</video:thumbnail_loc>
<video:description>if this gives someone a kickstart just like the great videos which in part are</video:description>
<video:content_loc>https://chemplayer.com/media/openchem.mp4</video:content_loc>
<video:duration>506.47</video:duration>
<video:rating>4.4</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/oxalic-acid-from-cane-sugar-and-nitric-acid</loc>
<video:video>
<video:title>Oxalic acid from cane sugar and nitric acid</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/oxalic-acid-from-cane-sugar-and-nitric-acid.jpg</video:thumbnail_loc>
<video:description>In this video we will prepare oxalic acid using an old-fashioned preparation</video:description>
<video:content_loc>https://chemplayer.com/media/oxalic-acid-from-cane-sugar-and-nitric-acid.mp4</video:content_loc>
<video:duration>282.35</video:duration>
<video:rating>3.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/phenyl-2-propanone-from-acetone-and-benzene</loc>
<video:video>
<video:title>Phenyl-2-propanone from acetone and benzene</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/phenyl-2-propanone-from-acetone-and-benzene.jpg</video:thumbnail_loc>
<video:description>In this video we're going to prepare a very notorious ketone, phenyl 2-propanone....For information about how to make this from zinc chloride, check out our other video linked.</video:description>
<video:content_loc>https://chemplayer.com/media/phenyl-2-propanone-from-acetone-and-benzene.mp4</video:content_loc>
<video:duration>866.13</video:duration>
<video:rating>4.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/phenylacetic-acid-from-mandelic-acid-via-hi-reduction</loc>
<video:video>
<video:title>Phenylacetic acid from mandelic acid via HI reduction</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/phenylacetic-acid-from-mandelic-acid-via-hi-reduction.jpg</video:thumbnail_loc>
<video:description>Check out our other video for full information on this.</video:description>
<video:content_loc>https://chemplayer.com/media/phenylacetic-acid-from-mandelic-acid-via-hi-reduction.mp4</video:content_loc>
<video:duration>545.0</video:duration>
<video:rating>4.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/phthalimide-preparation-from-phthalic-anhydride</loc>
<video:video>
<video:title>Phthalimide preparation from phthalic anhydride</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/phthalimide-preparation-from-phthalic-anhydride.jpg</video:thumbnail_loc>
<video:description>Thalamite is an extremely useful compound, which can be quickly, and easily produced from phthalic anhydride, the anhydride itself if, a common chemical, or you can also produce it yourself, by heating phthalic acid, until it forms a melt, the phthalic anhydride, should be an amorphous white solid, like, this, if you have crystals then your phthalic anhydride has, probably slowly absorbed water from the air and turned back, into phthalic acid, in which case you will have,...to, melt it and convert back into the anhydride again, start by weighing out, 35 grams of anhydride, there are two ways to produce thalamite, one involves extended, heating with ammonia solution, the other method uses urea, and, we find this to be the more convenient way,</video:description>
<video:content_loc>https://chemplayer.com/media/phthalimide-preparation-from-phthalic-anhydride.mp4</video:content_loc>
<video:duration>235.0</video:duration>
<video:rating>4.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/piperidine-from-the-sodium-metal-reduction-of-pyridine</loc>
<video:video>
<video:title>Piperidine from the sodium metal reduction of pyridine</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/piperidine-from-the-sodium-metal-reduction-of-pyridine.jpg</video:thumbnail_loc>
<video:description>ring of the pyridine to form pi-pyridine. A pretty serious reduction. And it's going to...oil isn't as dry as we thought. 56 grams is a lot of sodium metal. Nearly two and a half moles.</video:description>
<video:content_loc>https://chemplayer.com/media/piperidine-from-the-sodium-metal-reduction-of-pyridine.mp4</video:content_loc>
<video:duration>898.1</video:duration>
<video:rating>4.2</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/piperine-from-black-pepper-microwave-extraction</loc>
<video:video>
<video:title>Piperine from black pepper (microwave extraction)</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/piperine-from-black-pepper-microwave-extraction.jpg</video:thumbnail_loc>
<video:description>In this kemp layer we will be extracting piperine from peppercorns, white pepper is the best...to use because it usually contains a higher percentage of piperine and less</video:description>
<video:content_loc>https://chemplayer.com/media/piperine-from-black-pepper-microwave-extraction.mp4</video:content_loc>
<video:duration>620.3</video:duration>
<video:rating>4.5</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/piperine-hydrolysis-to-piperinic-acid-and-piperidine</loc>
<video:video>
<video:title>Piperine hydrolysis to piperinic acid and piperidine</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/piperine-hydrolysis-to-piperinic-acid-and-piperidine.jpg</video:thumbnail_loc>
<video:description>Check out our previous video for details of how we did this.</video:description>
<video:content_loc>https://chemplayer.com/media/piperine-hydrolysis-to-piperinic-acid-and-piperidine.mp4</video:content_loc>
<video:duration>871.35</video:duration>
<video:rating>3.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/piss-piss-bang-bang</loc>
<video:video>
<video:title>Piss piss bang bang</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/piss-piss-bang-bang.jpg</video:thumbnail_loc>
<video:description>As you know, organic compounds such as alcohols and acids which contain oxygen are more likely...So the alcohol in that beer we drank? Well it will have been oxidized very transiently</video:description>
<video:content_loc>https://chemplayer.com/media/piss-piss-bang-bang.mp4</video:content_loc>
<video:duration>815.0</video:duration>
<video:rating>4.4</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/potassium-chlorochromate-and-oxidation-of-benzyl-alcohol</loc>
<video:video>
<video:title>Potassium chlorochromate and oxidation of benzyl alcohol</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/potassium-chlorochromate-and-oxidation-of-benzyl-alcohol.jpg</video:thumbnail_loc>
<video:description>We made potassium dichromate in a previous video, so check this out for details of how...We won't show you how to convert this to pure benzaldehyde because we've done this before in a couple of videos.</video:description>
<video:content_loc>https://chemplayer.com/media/potassium-chlorochromate-and-oxidation-of-benzyl-alcohol.mp4</video:content_loc>
<video:duration>801.04</video:duration>
<video:rating>4.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/potassium-cyanate-and-reduction-to-cyanide</loc>
<video:video>
<video:title>Potassium cyanate and reduction to cyanide</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/potassium-cyanate-and-reduction-to-cyanide.jpg</video:thumbnail_loc>
<video:description>we're back from our vacation and today we'll be making potassium cyanate to do...grams of urea we're using urea here in a 2.2 molar ratio which apparently gives a good yield</video:description>
<video:content_loc>https://chemplayer.com/media/potassium-cyanate-and-reduction-to-cyanide.mp4</video:content_loc>
<video:duration>751.0</video:duration>
<video:rating>4.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/potassium-cyanide-preparation</loc>
<video:video>
<video:title>Potassium cyanide preparation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/potassium-cyanide-preparation.jpg</video:thumbnail_loc>
<video:description>out in the previous video we used ethanol to precipitate the cyanide salt but in this</video:description>
<video:content_loc>https://chemplayer.com/media/potassium-cyanide-preparation.mp4</video:content_loc>
<video:duration>859.0</video:duration>
<video:rating>3.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/potassium-thiocyanate-preparation</loc>
<video:video>
<video:title>Potassium thiocyanate preparation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/potassium-thiocyanate-preparation.jpg</video:thumbnail_loc>
<video:description>the dihydrate crystals. If you have these then dehydrate them in an oven at 150 degrees C for...powdered sulfur. In theory the reaction requires five mole equivalents of sulfur for each ferrocyanide</video:description>
<video:content_loc>https://chemplayer.com/media/potassium-thiocyanate-preparation.mp4</video:content_loc>
<video:duration>731.31</video:duration>
<video:rating>4.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/preparation-of-crude-benzyl-cyanide-from-benzyl-chloride</loc>
<video:video>
<video:title>Preparation of crude benzyl cyanide from benzyl chloride</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/preparation-of-crude-benzyl-cyanide-from-benzyl-chloride.jpg</video:thumbnail_loc>
<video:description>In this video we prepare benzyl cyanide using the cold netrile synthesis you'll...Check out our other video for details of how we, do this by heating potassium, ferrocyanide</video:description>
<video:content_loc>https://chemplayer.com/media/preparation-of-crude-benzyl-cyanide-from-benzyl-chloride.mp4</video:content_loc>
<video:duration>439.09</video:duration>
<video:rating>3.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/preparation-of-liquid-nitrogen-dioxide</loc>
<video:video>
<video:title>Preparation of liquid nitrogen dioxide</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/preparation-of-liquid-nitrogen-dioxide.jpg</video:thumbnail_loc>
<video:description>Today we're celebrating our 1000th Kimplaheer channel subscriber, and as a reward this video</video:description>
<video:content_loc>https://chemplayer.com/media/preparation-of-liquid-nitrogen-dioxide.mp4</video:content_loc>
<video:duration>667.13</video:duration>
<video:rating>4.4</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/preparation-of-nitrous-oxide-gas</loc>
<video:video>
<video:title>Preparation of nitrous oxide gas</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/preparation-of-nitrous-oxide-gas.jpg</video:thumbnail_loc>
<video:description>In this video we'll prepare nitrous oxide gas via the oxidation of a</video:description>
<video:content_loc>https://chemplayer.com/media/preparation-of-nitrous-oxide-gas.mp4</video:content_loc>
<video:duration>323.0</video:duration>
<video:rating>4.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/preparation-of-potassium-iodate</loc>
<video:video>
<video:title>Preparation of potassium iodate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/preparation-of-potassium-iodate.jpg</video:thumbnail_loc>
<video:description>In this video we're going to prepare Potassium Iodate starting with Potassium Chlorate.</video:description>
<video:content_loc>https://chemplayer.com/media/preparation-of-potassium-iodate.mp4</video:content_loc>
<video:duration>659.26</video:duration>
<video:rating>4.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/preparation-of-potassium-periodate</loc>
<video:video>
<video:title>Preparation of potassium periodate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/preparation-of-potassium-periodate.jpg</video:thumbnail_loc>
<video:description>That's all for this video.</video:description>
<video:content_loc>https://chemplayer.com/media/preparation-of-potassium-periodate.mp4</video:content_loc>
<video:duration>605.09</video:duration>
<video:rating>4.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/preparation-of-potassium-phthalimide</loc>
<video:video>
<video:title>Preparation of potassium phthalimide</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/preparation-of-potassium-phthalimide.jpg</video:thumbnail_loc>
<video:description>In this video we'll prepare potassium thalimide, the reagent we plan to use in a future video....To start we weighed out 17.5 grams of thalimide. Check out our other video for details of how to make this yourself from phthalic anhydride.</video:description>
<video:content_loc>https://chemplayer.com/media/preparation-of-potassium-phthalimide.mp4</video:content_loc>
<video:duration>381.02</video:duration>
<video:rating>4.2</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/preparation-of-propionyl-chloride</loc>
<video:video>
<video:title>Preparation of propionyl chloride</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/preparation-of-propionyl-chloride.jpg</video:thumbnail_loc>
<video:description>We are going to prepare propionyl chloride....Add the propionic acid to the dry flask and add a magnetic stir bar to the flask.</video:description>
<video:content_loc>https://chemplayer.com/media/preparation-of-propionyl-chloride.mp4</video:content_loc>
<video:duration>317.18</video:duration>
<video:rating>3.5</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/prepare-nano-copper-powder-using-ascorbic-acid-vitamin-c</loc>
<video:video>
<video:title>Prepare 'nano' copper powder using ascorbic acid (vitamin C)</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/prepare-nano-copper-powder-using-ascorbic-acid-vitamin-c.jpg</video:thumbnail_loc>
<video:description>in this experiment we are going to prepare nano copper nanometer scale fine...Now measure out 24 grams of ascorbic acid. We're using pure food grade vitamin C here which is the L-enantiomer of ascorbic acid.</video:description>
<video:content_loc>https://chemplayer.com/media/prepare-nano-copper-powder-using-ascorbic-acid-vitamin-c.mp4</video:content_loc>
<video:duration>441.0</video:duration>
<video:rating>3.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/prepare-aromatic-ketones-from-calcium-benzoate</loc>
<video:video>
<video:title>Prepare aromatic ketones from calcium benzoate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/prepare-aromatic-ketones-from-calcium-benzoate.jpg</video:thumbnail_loc>
<video:description>We did this reaction previously in a different video using calcium propionate and calcium benzoate to make propiothenone.</video:description>
<video:content_loc>https://chemplayer.com/media/prepare-aromatic-ketones-from-calcium-benzoate.mp4</video:content_loc>
<video:duration>895.29</video:duration>
<video:rating>4.5</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/prepare-isopropyl-nitrite</loc>
<video:video>
<video:title>Prepare isopropyl nitrite</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/prepare-isopropyl-nitrite.jpg</video:thumbnail_loc>
<video:description>prepare isopropyl nitrate....Start by weighing 72 grams of sodium nitrite and dissolve in 120 ml of water.</video:description>
<video:content_loc>https://chemplayer.com/media/prepare-isopropyl-nitrite.mp4</video:content_loc>
<video:duration>294.0</video:duration>
<video:rating>3.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/prepare-solid-iodine</loc>
<video:video>
<video:title>Prepare solid iodine</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/prepare-solid-iodine.jpg</video:thumbnail_loc>
<video:description>We will prepare extremely useful solid iodine...using a very quick and simple reaction involving potassium iodide and a</video:description>
<video:content_loc>https://chemplayer.com/media/prepare-solid-iodine.mp4</video:content_loc>
<video:duration>200.0</video:duration>
<video:rating>3.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/prepare-solid-iodine-with-james-earl-jones</loc>
<video:video>
<video:title>Prepare solid iodine (with James Earl Jones)</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/prepare-solid-iodine-with-james-earl-jones.jpg</video:thumbnail_loc>
<video:description>undefined</video:description>
<video:content_loc>https://chemplayer.com/media/prepare-solid-iodine-with-james-earl-jones.mp4</video:content_loc>
<video:duration>200.0</video:duration>
<video:rating>4.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/prepare-succinic-acid-from-monosodium-glutamate</loc>
<video:video>
<video:title>Prepare succinic acid from monosodium glutamate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/prepare-succinic-acid-from-monosodium-glutamate.jpg</video:thumbnail_loc>
<video:description>today we're starting with a very common food additive msg or monosodium...first thing we're going to do is convert this into the more useful glutamic acid</video:description>
<video:content_loc>https://chemplayer.com/media/prepare-succinic-acid-from-monosodium-glutamate.mp4</video:content_loc>
<video:duration>618.0</video:duration>
<video:rating>4.4</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/prepare-urea-hydrogen-peroxide-crystalline-adduct</loc>
<video:video>
<video:title>Prepare urea-hydrogen peroxide crystalline adduct</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/prepare-urea-hydrogen-peroxide-crystalline-adduct.jpg</video:thumbnail_loc>
<video:description>We going to start today by preparing a useful reagent, carbamide peroxide....Instead of the crystals forming a water-hydrated salt, they trap hydrogen peroxide instead of form of solid adduct.</video:description>
<video:content_loc>https://chemplayer.com/media/prepare-urea-hydrogen-peroxide-crystalline-adduct.mp4</video:content_loc>
<video:duration>277.0</video:duration>
<video:rating>4.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/preparing-guanidine-from-ammonium-thiocyanate</loc>
<video:video>
<video:title>Preparing guanidine from ammonium thiocyanate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/preparing-guanidine-from-ammonium-thiocyanate.jpg</video:thumbnail_loc>
<video:description>in this video we're going to have a go at making guanidine guanidine is an</video:description>
<video:content_loc>https://chemplayer.com/media/preparing-guanidine-from-ammonium-thiocyanate.mp4</video:content_loc>
<video:duration>709.23</video:duration>
<video:rating>4.4</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/preparing-our-favourite-psychoactive-substance</loc>
<video:video>
<video:title>Preparing our favourite psychoactive substance</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/preparing-our-favourite-psychoactive-substance.jpg</video:thumbnail_loc>
<video:description>drug thanks for watching and we hope you enjoyed this video and learn need</video:description>
<video:content_loc>https://chemplayer.com/media/preparing-our-favourite-psychoactive-substance.mp4</video:content_loc>
<video:duration>750.05</video:duration>
<video:rating>3.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/propionic-anhydride-testing-two-preparation-methods</loc>
<video:video>
<video:title>Propionic anhydride - testing two preparation methods</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/propionic-anhydride-testing-two-preparation-methods.jpg</video:thumbnail_loc>
<video:description>Hope you enjoyed this video.</video:description>
<video:content_loc>https://chemplayer.com/media/propionic-anhydride-testing-two-preparation-methods.mp4</video:content_loc>
<video:duration>799.0</video:duration>
<video:rating>3.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/propiophenone-synthesis-from-benzene-and-propionyl-chloride</loc>
<video:video>
<video:title>Propiophenone synthesis from benzene and propionyl chloride</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/propiophenone-synthesis-from-benzene-and-propionyl-chloride.jpg</video:thumbnail_loc>
<video:description>In this video, we'll synthesize propiophenone</video:description>
<video:content_loc>https://chemplayer.com/media/propiophenone-synthesis-from-benzene-and-propionyl-chloride.mp4</video:content_loc>
<video:duration>526.26</video:duration>
<video:rating>5.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/propiophenone-synthesis-from-benzene-and-propionyl-chloride-with-james-earl-jones</loc>
<video:video>
<video:title>Propiophenone synthesis from benzene and propionyl chloride with James Earl Jones</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/propiophenone-synthesis-from-benzene-and-propionyl-chloride.jpg</video:thumbnail_loc>
<video:description>undefined</video:description>
<video:content_loc>https://chemplayer.com/media/propiophenone-synthesis-from-benzene-and-propionyl-chloride-with-james-earl-jones.mp4</video:content_loc>
<video:duration>526.26</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/pyridine-hydrochloride-and-can-it-demethylate-vanillin</loc>
<video:video>
<video:title>Pyridine hydrochloride, and can it demethylate vanillin</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/pyridine-hydrochloride-and-can-it-demethylate-vanillin.jpg</video:thumbnail_loc>
<video:description>You can make pyridine hydrochloride by bubbling dry HCl gas through an ether solution of pyridine....So let's get the flask set up in there and we'll get the pyridine chilling down.</video:description>
<video:content_loc>https://chemplayer.com/media/pyridine-hydrochloride-and-can-it-demethylate-vanillin.mp4</video:content_loc>
<video:duration>892.09</video:duration>
<video:rating>4.3</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/radical-alkylation-using-manganese-iii-acetate</loc>
<video:video>
<video:title>Radical alkylation using manganese (III) acetate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/radical-alkylation-using-manganese-iii-acetate.jpg</video:thumbnail_loc>
<video:description>We're going to try this out in this video.</video:description>
<video:content_loc>https://chemplayer.com/media/radical-alkylation-using-manganese-iii-acetate.mp4</video:content_loc>
<video:duration>899.0</video:duration>
<video:rating>4.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/reduction-of-trichloroacetic-acid-using-zinc</loc>
<video:video>
<video:title>Reduction of trichloroacetic acid using zinc</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/reduction-of-trichloroacetic-acid-using-zinc.jpg</video:thumbnail_loc>
<video:description>trichloroacetic acid crystals take care with this as the pure acid is a strong...can react with a suitably reactive metal and form hydrogen gas you've probably</video:description>
<video:content_loc>https://chemplayer.com/media/reduction-of-trichloroacetic-acid-using-zinc.mp4</video:content_loc>
<video:duration>860.44</video:duration>
<video:rating>3.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/reduction-of-vanillin-to-vanillyl-alcohol</loc>
<video:video>
<video:title>Reduction of vanillin to vanillyl alcohol</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/reduction-of-vanillin-to-vanillyl-alcohol.jpg</video:thumbnail_loc>
<video:description>can easily be oxidized to the corresponding carboxylic acid, but it can...and 99% pure. As you can see from the structure, vanillin is a phenol</video:description>
<video:content_loc>https://chemplayer.com/media/reduction-of-vanillin-to-vanillyl-alcohol.mp4</video:content_loc>
<video:duration>887.0</video:duration>
<video:rating>4.2</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/reduction-of-vanillin-nitroethane-condensation-product-with-borohydride</loc>
<video:video>
<video:title>Reduction of vanillin-nitroethane condensation product with borohydride</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/reduction-of-vanillin-nitroethane-condensation-product-with-borohydride.jpg</video:thumbnail_loc>
<video:description>Next measure out 40 mils of ethyl acetate. This has a habit of sucking up...same reduction using tin chloride. Worth looking into. Add the borohydride to the solvent in</video:description>
<video:content_loc>https://chemplayer.com/media/reduction-of-vanillin-nitroethane-condensation-product-with-borohydride.mp4</video:content_loc>
<video:duration>636.0</video:duration>
<video:rating>4.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/semicarbazide-from-the-reduction-of-nitrourea</loc>
<video:video>
<video:title>Semicarbazide from the reduction of nitrourea</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/semicarbazide-from-the-reduction-of-nitrourea.jpg</video:thumbnail_loc>
<video:description>in a previous video we prepared nitro urea today we're going to take this</video:description>
<video:content_loc>https://chemplayer.com/media/semicarbazide-from-the-reduction-of-nitrourea.mp4</video:content_loc>
<video:duration>899.0</video:duration>
<video:rating>3.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/separating-paracetamol-and-codeine-from-strong-analgesic-tablets</loc>
<video:video>
<video:title>Separating paracetamol and codeine from strong analgesic tablets</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/separating-paracetamol-and-codeine-from-strong-analgesic-tablets.jpg</video:thumbnail_loc>
<video:description>Each tablet contains 500 mg of paracetamol and 30 mg of codeine phosphate....Paracetamol is fairly temperature-stable, but codeine is a delicate substance, so we want to be careful we don't heat it above about 70 degrees C for too long.</video:description>
<video:content_loc>https://chemplayer.com/media/separating-paracetamol-and-codeine-from-strong-analgesic-tablets.mp4</video:content_loc>
<video:duration>881.31</video:duration>
<video:rating>4.5</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/sodium-bromate-oxidation-of-tetrahydrofuran</loc>
<video:video>
<video:title>Sodium bromate oxidation of tetrahydrofuran</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/sodium-bromate-oxidation-of-tetrahydrofuran.jpg</video:thumbnail_loc>
<video:description>This is a viewer's suggestion to see if tetrahydrofuran can be oxidized by sodium bromate...Here's some sodium bromate crystals</video:description>
<video:content_loc>https://chemplayer.com/media/sodium-bromate-oxidation-of-tetrahydrofuran.mp4</video:content_loc>
<video:duration>898.0</video:duration>
<video:rating>4.3</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/sodium-percarbonate-preparation</loc>
<video:video>
<video:title>Sodium percarbonate preparation</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/sodium-percarbonate-preparation.jpg</video:thumbnail_loc>
<video:description>In this video we're going to create another hydrogen peroxide adduct, only this time with</video:description>
<video:content_loc>https://chemplayer.com/media/sodium-percarbonate-preparation.mp4</video:content_loc>
<video:duration>552.05</video:duration>
<video:rating>3.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/sodium-potassium-cyanide</loc>
<video:video>
<video:title>Sodium-potassium cyanide</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/sodium-potassium-cyanide.jpg</video:thumbnail_loc>
<video:description>wrong the preparation involves a reaction between potassium ferrocyanide...this one first of all measure out 40 grams exactly of anhydrous potassium</video:description>
<video:content_loc>https://chemplayer.com/media/sodium-potassium-cyanide.mp4</video:content_loc>
<video:duration>391.26</video:duration>
<video:rating>4.4</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/sulfuric-acid-from-sulfur-using-hydrogen-peroxide</loc>
<video:video>
<video:title>Sulfuric acid from sulfur using hydrogen peroxide</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/sulfuric-acid-from-sulfur-using-hydrogen-peroxide.jpg</video:thumbnail_loc>
<video:description>we recently got hold of some really nice quality sulfur but we couldn't think of...had some old hydrogen the rock side solution of unknown strength lying around so we thought we'd</video:description>
<video:content_loc>https://chemplayer.com/media/sulfuric-acid-from-sulfur-using-hydrogen-peroxide.mp4</video:content_loc>
<video:duration>416.0</video:duration>
<video:rating>4.3</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/supporting-chemplayer-in-2016-research-projects</loc>
<video:video>
<video:title>Supporting ChemPlayer in 2016 + Research projects</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/supporting-chemplayer-in-2016-research-projects.jpg</video:thumbnail_loc>
<video:description>We want to keep this project going and bring you more interesting experiments and videos.</video:description>
<video:content_loc>https://chemplayer.com/media/supporting-chemplayer-in-2016-research-projects.mp4</video:content_loc>
<video:duration>293.0</video:duration>
<video:rating>4.1</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/synthesis-of-a-piperidine-ephedrone-analogue</loc>
<video:video>
<video:title>Synthesis of a piperidine ephedrone analogue</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/synthesis-of-a-piperidine-ephedrone-analogue.jpg</video:thumbnail_loc>
<video:description>Check out our other video for details of how to make this yourself.</video:description>
<video:content_loc>https://chemplayer.com/media/synthesis-of-a-piperidine-ephedrone-analogue.mp4</video:content_loc>
<video:duration>870.31</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/synthesis-of-a-piperidine-ephedrone-analogue-with-james-earl-jones</loc>
<video:video>
<video:title>Synthesis of a piperidine ephedrone analogue - with James Earl Jones</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/synthesis-of-a-piperidine-ephedrone-analogue.jpg</video:thumbnail_loc>
<video:description>undefined</video:description>
<video:content_loc>https://chemplayer.com/media/synthesis-of-a-piperidine-ephedrone-analogue-with-james-earl-jones.mp4</video:content_loc>
<video:duration>870.31</video:duration>
<video:rating>4.3</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/synthesis-of-a-quinazolinone-heterocycle</loc>
<video:video>
<video:title>Synthesis of a quinazolinone heterocycle</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/synthesis-of-a-quinazolinone-heterocycle.jpg</video:thumbnail_loc>
<video:description>In this video we're going to synthesize a quinazolinone heterosilic compound using acetoanthanilic</video:description>
<video:content_loc>https://chemplayer.com/media/synthesis-of-a-quinazolinone-heterocycle.mp4</video:content_loc>
<video:duration>697.0</video:duration>
<video:rating>4.3</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/synthesis-of-anisole-from-phenol-and-methyl-iodide</loc>
<video:video>
<video:title>Synthesis of anisole from phenol and methyl iodide</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/synthesis-of-anisole-from-phenol-and-methyl-iodide.jpg</video:thumbnail_loc>
<video:description>iodide and phenol, using a strong base....Add the methanol into a flask equipped with a thermometer, and stir bar.</video:description>
<video:content_loc>https://chemplayer.com/media/synthesis-of-anisole-from-phenol-and-methyl-iodide.mp4</video:content_loc>
<video:duration>593.18</video:duration>
<video:rating>3.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/synthesis-of-anthranilic-acid-via-hofmann-rearrangement</loc>
<video:video>
<video:title>Synthesis of anthranilic acid via Hofmann rearrangement</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/synthesis-of-anthranilic-acid-via-hofmann-rearrangement.jpg</video:thumbnail_loc>
<video:description>With stirring and the temperature at around 10 degrees C, add the thalamide powder to...the sodium hydroxide.</video:description>
<video:content_loc>https://chemplayer.com/media/synthesis-of-anthranilic-acid-via-hofmann-rearrangement.mp4</video:content_loc>
<video:duration>379.34</video:duration>
<video:rating>3.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/synthesis-of-benzil-from-benzoin</loc>
<video:video>
<video:title>Synthesis of benzil from benzoin</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/synthesis-of-benzil-from-benzoin.jpg</video:thumbnail_loc>
<video:description>In the previous video we showed you how to prepare benzoin from benzaldehyde using a cyanide catalyst....You can also use thiamine as a more OTC catalyst for that reaction.</video:description>
<video:content_loc>https://chemplayer.com/media/synthesis-of-benzil-from-benzoin.mp4</video:content_loc>
<video:duration>588.0</video:duration>
<video:rating>3.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/synthesis-of-benzilic-acid-from-benzil</loc>
<video:video>
<video:title>Synthesis of benzilic acid from benzil</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/synthesis-of-benzilic-acid-from-benzil.jpg</video:thumbnail_loc>
<video:description>In our previous video we prepared benzyl via the reaction from benzoin, which in...turn was prepared from benzaldehyde which we prepared before in a few different videos.</video:description>
<video:content_loc>https://chemplayer.com/media/synthesis-of-benzilic-acid-from-benzil.mp4</video:content_loc>
<video:duration>765.47</video:duration>
<video:rating>4.1</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/synthesis-of-benzocaine</loc>
<video:video>
<video:title>Synthesis of benzocaine</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/synthesis-of-benzocaine.jpg</video:thumbnail_loc>
<video:description>In this video we're going to do a few more reactions with this and transform it into something very interesting....In a video we did recently we checked out a few different ways to do this reduction</video:description>
<video:content_loc>https://chemplayer.com/media/synthesis-of-benzocaine.mp4</video:content_loc>
<video:duration>885.17</video:duration>
<video:rating>3.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/synthesis-of-chlorbutol-from-chloroform-and-acetone</loc>
<video:video>
<video:title>Synthesis of chlorbutol from chloroform and acetone</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/synthesis-of-chlorbutol-from-chloroform-and-acetone.jpg</video:thumbnail_loc>
<video:description>In this video we'll prepare chlorbutol, a very old fashioned medicine used as an antiseptic</video:description>
<video:content_loc>https://chemplayer.com/media/synthesis-of-chlorbutol-from-chloroform-and-acetone.mp4</video:content_loc>
<video:duration>394.0</video:duration>
<video:rating>4.1</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/synthesis-of-mandelic-acid-from-benzaldehyde</loc>
<video:video>
<video:title>Synthesis of mandelic acid from benzaldehyde</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/synthesis-of-mandelic-acid-from-benzaldehyde.jpg</video:thumbnail_loc>
<video:description>First measure out 15 grams of benzaldehyde ours is a bit discolored but relatively pure...and free from benzoic acid.</video:description>
<video:content_loc>https://chemplayer.com/media/synthesis-of-mandelic-acid-from-benzaldehyde.mp4</video:content_loc>
<video:duration>573.42</video:duration>
<video:rating>4.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/synthesis-of-parabanic-acid</loc>
<video:video>
<video:title>Synthesis of parabanic acid</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/synthesis-of-parabanic-acid.jpg</video:thumbnail_loc>
<video:description>In this video, we're going to be preparing an interesting heterocyclic compound called...reagent is thymethyloxylate. We prepared this in a video not so long ago, so if you want more</video:description>
<video:content_loc>https://chemplayer.com/media/synthesis-of-parabanic-acid.mp4</video:content_loc>
<video:duration>733.0</video:duration>
<video:rating>3.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/synthesis-of-phenytoin-an-anti-seizure-drug</loc>
<video:video>
<video:title>Synthesis of phenytoin; an anti-seizure drug</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/synthesis-of-phenytoin-an-anti-seizure-drug.jpg</video:thumbnail_loc>
<video:description>In this video, we're going to perform another experiment with Benz-Yl....We prepared this using the procedure we covered in a previous video.</video:description>
<video:content_loc>https://chemplayer.com/media/synthesis-of-phenytoin-an-anti-seizure-drug.mp4</video:content_loc>
<video:duration>685.0</video:duration>
<video:rating>4.3</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/synthesis-of-sodium-ethyl-nitrophenylpyruvate</loc>
<video:video>
<video:title>Synthesis of sodium ethyl nitrophenylpyruvate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/synthesis-of-sodium-ethyl-nitrophenylpyruvate.jpg</video:thumbnail_loc>
<video:description>We prepared this in the previous video by reacting ethanol and anhydroxalic acid, so...Again, we prepared this back in our first ever completer video by nitrating toluene and</video:description>
<video:content_loc>https://chemplayer.com/media/synthesis-of-sodium-ethyl-nitrophenylpyruvate.mp4</video:content_loc>
<video:duration>681.0</video:duration>
<video:rating>4.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/testing-otc-friedel-crafts-catalysts</loc>
<video:video>
<video:title>Testing OTC Friedel-Crafts catalysts</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/testing-otc-friedel-crafts-catalysts.jpg</video:thumbnail_loc>
<video:description>Check out some of our other videos for details of how to make this.</video:description>
<video:content_loc>https://chemplayer.com/media/testing-otc-friedel-crafts-catalysts.mp4</video:content_loc>
<video:duration>732.0</video:duration>
<video:rating>4.2</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/the-maillard-reaction</loc>
<video:video>
<video:title>The Maillard reaction</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/the-maillard-reaction.jpg</video:thumbnail_loc>
<video:description>I'll show you how you can extract pure piperine from black pepper in a previous video....And then it's time to add the brandy and we'll light the alcohol and flambe the mixture.</video:description>
<video:content_loc>https://chemplayer.com/media/the-maillard-reaction.mp4</video:content_loc>
<video:duration>892.0</video:duration>
<video:rating>3.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/the-aromatic-nitro-reduction-contest</loc>
<video:video>
<video:title>The aromatic nitro reduction contest</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/the-aromatic-nitro-reduction-contest.jpg</video:thumbnail_loc>
<video:description>tin and hydrochloric acid. We've done this in the previous video so check it out for more information.</video:description>
<video:content_loc>https://chemplayer.com/media/the-aromatic-nitro-reduction-contest.mp4</video:content_loc>
<video:duration>898.33</video:duration>
<video:rating>4.8</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/theobromine-extraction-from-cocoa-powder</loc>
<video:video>
<video:title>Theobromine extraction from cocoa powder</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/theobromine-extraction-from-cocoa-powder.jpg</video:thumbnail_loc>
<video:description>caffeine from coffee. Caffeine is a xanthate stimulant. Today we're going to extract a...different xanthate stimulant, theobromine, and we're going to be starting with cocoa powder</video:description>
<video:content_loc>https://chemplayer.com/media/theobromine-extraction-from-cocoa-powder.mp4</video:content_loc>
<video:duration>569.1</video:duration>
<video:rating>5.0</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/time-for-a-pick-me-up-tiramisu</loc>
<video:video>
<video:title>Time for a pick-me-up; Tiramisu!</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/time-for-a-pick-me-up-tiramisu.jpg</video:thumbnail_loc>
<video:description>There's no end music on this video.</video:description>
<video:content_loc>https://chemplayer.com/media/time-for-a-pick-me-up-tiramisu.mp4</video:content_loc>
<video:duration>892.0</video:duration>
<video:rating>4.6</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/tips-on-equipping-your-own-mini-lab</loc>
<video:video>
<video:title>Tips on equipping your own mini-lab</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/tips-on-equipping-your-own-mini-lab.jpg</video:thumbnail_loc>
<video:description>ours are polycarbonate ones from a hardware store then we have light...We are lucky enough to have about 10 of these pro quality 100 mil Duran storage containers,</video:description>
<video:content_loc>https://chemplayer.com/media/tips-on-equipping-your-own-mini-lab.mp4</video:content_loc>
<video:duration>737.0</video:duration>
<video:rating>4.4</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/toluidine-via-the-reduction-of-nitrotoluene</loc>
<video:video>
<video:title>Toluidine via the reduction of nitrotoluene</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/toluidine-via-the-reduction-of-nitrotoluene.jpg</video:thumbnail_loc>
<video:description>In this video we'll prepare ortho-toluidine by reducing ortho-nitric</video:description>
<video:content_loc>https://chemplayer.com/media/toluidine-via-the-reduction-of-nitrotoluene.mp4</video:content_loc>
<video:duration>439.44</video:duration>
<video:rating>4.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/trying-out-a-preparation-of-phenylacetic-acid</loc>
<video:video>
<video:title>Trying out a preparation of phenylacetic acid</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/trying-out-a-preparation-of-phenylacetic-acid.jpg</video:thumbnail_loc>
<video:description>video, but this time we're going to try a different procedure to see if we can get a...We've prepared this in the previous video from benzoyl alcohol, so check it out at the</video:description>
<video:content_loc>https://chemplayer.com/media/trying-out-a-preparation-of-phenylacetic-acid.mp4</video:content_loc>
<video:duration>899.22</video:duration>
<video:rating>4.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/two-more-attempts-to-make-vanillyl-nitrile</loc>
<video:video>
<video:title>Two more attempts to make vanillyl nitrile</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/two-more-attempts-to-make-vanillyl-nitrile.jpg</video:thumbnail_loc>
<video:description>In fact we've done this in a previous video with exactly these two reagents....We prepared this in a previous video by reacting sodium acetate and acetyl chloride, so check</video:description>
<video:content_loc>https://chemplayer.com/media/two-more-attempts-to-make-vanillyl-nitrile.mp4</video:content_loc>
<video:duration>875.0</video:duration>
<video:rating>4.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/o-nitrotoluene-using-nitric-acid-in-dcm</loc>
<video:video>
<video:title>o-Nitrotoluene using nitric acid in DCM</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/o-nitrotoluene-using-nitric-acid-in-dcm.jpg</video:thumbnail_loc>
<video:description>Today we're going to try out an experimental procedure which claims to be able to nitrate toluene selectively in the ortho position....The reagent is nitric acid dissolved in dichloromethane.</video:description>
<video:content_loc>https://chemplayer.com/media/o-nitrotoluene-using-nitric-acid-in-dcm.mp4</video:content_loc>
<video:duration>753.0</video:duration>
<video:rating>4.3</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
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<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/p-nitrobenzoic-acid-from-p-nitrotoluene-using-dichromate</loc>
<video:video>
<video:title>p-Nitrobenzoic acid from p-nitrotoluene using dichromate</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/p-nitrobenzoic-acid-from-p-nitrotoluene-using-dichromate.jpg</video:thumbnail_loc>
<video:description>In this video we're going to oxidize this to pyrro nitro benzoic acid.</video:description>
<video:content_loc>https://chemplayer.com/media/p-nitrobenzoic-acid-from-p-nitrotoluene-using-dichromate.mp4</video:content_loc>
<video:duration>696.02</video:duration>
<video:rating>3.9</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
<url>
<loc>https://chemplayer.com/p-nitrobenzoic-acid-from-p-nitrotoluene-using-dichromate-narrated-by-james-earl-jones</loc>
<video:video>
<video:title>p-Nitrobenzoic acid from p-nitrotoluene using dichromate (narrated by James Earl Jones)</video:title>
<video:thumbnail_loc>https://chemplayer.com/media/p-nitrobenzoic-acid-from-p-nitrotoluene-using-dichromate-narrated-by-james-earl-jones.jpg</video:thumbnail_loc>
<video:description>undefined</video:description>
<video:content_loc>https://chemplayer.com/media/p-nitrobenzoic-acid-from-p-nitrotoluene-using-dichromate-narrated-by-james-earl-jones.mp4</video:content_loc>
<video:duration>696.02</video:duration>
<video:rating>4.7</video:rating>
<video:live>no</video:live>
</video:video>
<lastmod>2025-12-07T12:51:56.265Z</lastmod>
<changefreq>daily</changefreq>
<priority>1</priority>
</url>
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