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  2. Potassium permanganate - Wikipedia

    en.wikipedia.org/wiki/Potassium_permanganate

    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 ...

  3. Glycol cleavage - Wikipedia

    en.wikipedia.org/wiki/Glycol_cleavage

    Warm concentrated potassium permanganate (KMnO 4) will react with an alkene to form a glycol. Following this dihydroxylation , the KMnO 4 can then cleave the glycol to give aldehydes or ketones. The aldehydes will react further with (KMnO 4 ), being oxidized to become carboxylic acids .

  4. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    The oxidation of primary alcohols to carboxylic acids normally proceeds via the corresponding aldehyde, which is transformed via an aldehyde hydrate (gem-diol, R-CH(OH) 2) by reaction with water. Thus, the oxidation of a primary alcohol at the aldehyde level without further oxidation to the carboxylic acid is possible by performing the reaction ...

  5. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    When treated with a hot concentrated, acidified solution of KMnO 4, alkenes are cleaved to form ketones and/or carboxylic acids. The stoichiometry of the reaction is sensitive to conditions. This reaction and the ozonolysis can be used to determine the position of a double bond in an unknown alkene.

  6. Permanganate - Wikipedia

    en.wikipedia.org/wiki/Permanganate

    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 carboxylic acid, [12] oxalic acid to carbon dioxide, [13] and an alkene to a diol. [14] This list is not exhaustive. In alkene oxidations one intermediate is a cyclic Mn(V) species: [15]

  7. Dihydroxylation - Wikipedia

    en.wikipedia.org/wiki/Dihydroxylation

    Dihydroxylation is the process by which an alkene is converted into a vicinal diol.Although there are many routes to accomplish this oxidation, the most common and direct processes use a high-oxidation-state transition metal (typically osmium or manganese).

  8. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3. If a higher priority group is present (such as an aldehyde , ketone , or carboxylic acid ), then the prefix hydroxy- is used, [ 19 ] e.g., as in 1-hydroxy-2 ...

  9. Syn and anti addition - Wikipedia

    en.wikipedia.org/wiki/Syn_and_anti_addition

    When alkenes undergo hydrobromination, the alkyl bromides are formed Markovnikov. Alkyne oxymercuration-demercuration: In this reaction, HgSO 4 reacts with an alkyne in a Markovnikov regioselective manner to form an enol that is tautomerized into a ketone. This process utilizes anti addition of an OH group to the more substituted carbon, making ...