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• Alcohol
  ...c acids can be carried out using [[potassium permanganate]] or the [[Jones reagent]].
  6 KB (832 words) - 21:26, 29 June 2019
• Jones oxidation
  [[File:Jones oxidation-0.png|thumb|328x328px|Left: Freshly prepared Jones reagent. Right: The end products, with the color of chromium(III) indicating comple ...the latter to [[carboxylic acid]]s. The alcohol is acted upon by the Jones reagent, which consists of [[chromium trioxide]] or [[potassium dichromate]] dissol
  5 KB (879 words) - 18:55, 11 July 2019
• 2-Octanone
  The simplest method of preparing 2-octanol is by the [[Jones oxidation]] of 2-octanol.<br> Complete neutralization can be done with an oxidizing mixture, like Fenton's reagent, by adding it in small amounts. Since it's not very flammable, it should be
  5 KB (542 words) - 21:21, 13 September 2020
• Sec-Butanol
  sec-Butanol can be oxidized to butanone aka methyl ethyl ketone using Jones reagent.
  4 KB (506 words) - 18:40, 27 May 2023
• Carboxylic acid
  ...e presence of sulfuric acid will give their respective carboxylic acids. [[Jones oxidation]] is another route. Carbonation of a [[Grignard reagent|Grignard]] and organolithium reagents, followed by acidification:
  4 KB (526 words) - 13:34, 31 December 2021
• Redox
  *[[Jones oxidation]] *''Miscellaneous'': [[bromine water]], [[Fenton's reagent]], Frémy's salt, [[lead(IV) acetate]]
  4 KB (400 words) - 15:01, 2 January 2022
• Ketone
  ...lic addition upon the carbonyl is common, as in the reaction of [[Grignard reagent]]s with ketones. They form adducts with bisulfite and hydroxylamine, a prop Ketones can be easily prepared through the [[Jones oxidation]] of secondary alcohols, using [[chromium trioxide]] or [[potassi
  3 KB (428 words) - 22:37, 10 June 2018
• Khusimol
  As it contains a primary alcohol, khusimol can be oxidized with the Jones reagent to its respective carboxylic acid.
  4 KB (402 words) - 22:46, 30 July 2023