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Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.
Addition of concentrated sulfuric acid to potassium permanganate gives Mn 2 O 7. [76] Although no reaction may be apparent, the vapor over the mixture will ignite paper impregnated with alcohol. Potassium permanganate and sulfuric acid react to produce some ozone, which has a high oxidizing power and rapidly oxidizes the alcohol, causing it to ...
The exothermic (heat producing) reaction between potassium permanganate (KMnO 4), a strong oxidizing agent, and glycerol (C 3 H 5 (OH) 3), a readily oxidised organic substance, is an example of an experiment sometimes referred to as a "chemical volcano". [7] [8]
For instance, potassium permanganate decomposes at 230 °C to potassium manganate and manganese dioxide, releasing oxygen gas: 2 KMnO 4 → K 2 MnO 4 + MnO 2 + O 2 A permanganate can oxidize an amine to a nitro compound , [ 7 ] [ 8 ] an alcohol to a ketone , [ 9 ] an aldehyde to a carboxylic acid , [ 10 ] [ 11 ] a terminal alkene to a ...
The chemical chameleon reaction shows the process in reverse, by reducing violet potassium permanganate first to green potassium manganate and eventually to brown manganese dioxide: [1] [2] [5] KMnO 4 (violet) → K 2 MnO 4 (green) → MnO 2 (brown/yellow suspension) Blue potassium hypomanganate may also form as an intermediate. [6]
Potassium permanganate will decompose into potassium manganate, manganese dioxide and oxygen gas: 2 KMnO 4 → K 2 MnO 4 + MnO 2 + O 2. This reaction is a laboratory method to prepare oxygen, but produces samples of potassium manganate contaminated with MnO 2. The former is soluble and the latter is not.
The reaction initially produces permanganic acid, HMnO 4 (structurally, HOMnO 3), which is dehydrated by cold sulfuric acid to form its anhydride, Mn 2 O 7: 2 KMnO 4 + 2 H 2 SO 4 → Mn 2 O 7 + H 2 O + 2 KHSO 4. Mn 2 O 7 can react further with sulfuric acid to give the remarkable manganyl(VII) cation MnO + 3, which is isoelectronic with CrO 3:
[1] [2] The initial reaction product is a dihydropyridine which can be oxidized in a subsequent step to a pyridine. [3] The driving force for this second reaction step is aromatization. This reaction was reported in 1881 by Arthur Rudolf Hantzsch. A 1,4-dihydropyridine dicarboxylate is also called a 1,4-DHP compound or a Hantzsch ester.