tags
sodiumbenzoic acidDichromatechromic acidbenzenenitrotoluenemanganatenitrotolpyrropersulfatechromium saltsdichromatechromium

video tutorial p-Nitrobenzoic acid from p-nitrotoluene using dichromate

  • Starting from pyrro nitro toluene, the video oxidizes it to pyrro nitro benzoic acid using potassium dichromate in sulfuric acid.
  • The reaction setup includes a pressure-equalized addition funnel, controlled acid addition, and heating with reflux; the mixture turns from milky to a brown color as dichromate dissolves.
  • After acid addition, the mixture is heated for about 20 more minutes with gentle reflux; distillate appears milky due to unreacted nitrotoluene.
  • Post-reaction workup involves cooling, precipitation by ice, filtration, and drying to give a crude green/brown solid (about 12 g) containing chromium salts.
  • Purification via a hydroxide treatment converts the product to its sodium salt, precipitating chromium as hydroxide; subsequent acidification with HCl regenerates the product as a green solid.
  • Final isolated product: 8.8 g of pyrro nitro benzoic acid, about 85% yield from starting nitrotoluene; color described as yellow, with trace chromium salts.
  • Note: process carries hazards (strong oxidant, heat, fumes); scale-up requires caution.

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