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As an example, electrolysis of acetic acid yields ethane and carbon dioxide: CH 3 COOH → CH 3 COO − → CH 3 COO· → CH 3 · + CO 2 2CH 3 · → CH 3 CH 3. Another example is the synthesis of 2,7-dimethyl-2,7-dinitrooctane from 4-methyl-4-nitrovaleric acid: [3] The Kolbe reaction has also been occasionally used in cross-coupling reactions.
A well-known electrosynthesis is the Kolbe electrolysis, in which two carboxylic acids decarboxylate, and the remaining structures bond together: A variation is called the non-Kolbe reaction when a heteroatom (nitrogen or oxygen) is present at the α-position. The intermediate oxonium ion is trapped by a nucleophile, usually solvent.
2-ketoglutaric acid 2-oxoglutaric acid oxoglutaric acid: HOOC(CH 2) 2 COCOOH 3-oxopentanedioic acid: acetonedicarboxylic acid 3-oxoglutaric acid β-ketoglutaric acid 3-ketoglutaric acid: HOOCCH 2 COCH 2 COOH furan-2-carboxylic acid: 2-furoic acid α-furoic acid pyromucic acid 2-carboxyfuran α-furancarboxylic acid: furyl-COOH tetrahydrofuran-2 ...
In organic chemistry, a carboxylic acid is an organic acid that contains a carboxyl group (−C(=O)−OH) [1] attached to an R-group. The general formula of a carboxylic acid is often written as R−COOH or R−CO 2 H, sometimes as R−C(O)OH with R referring to an organyl group (e.g., alkyl, alkenyl, aryl), or hydrogen, or other groups ...
Dimers of carboxylic acids are often found in the vapour phase. Anhydrous carboxylic acids form dimers by hydrogen bonding of the acidic hydrogen and the carbonyl oxygen. For example, acetic acid forms a dimer in the gas phase, where the monomer units are held together by hydrogen bonds. [3] Many OH-containing molecules form dimers, e.g. the ...
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.
The Koch reaction is an organic reaction for the synthesis of tertiary carboxylic acids from alcohols or alkenes and carbon monoxide.Some commonly industrially produced Koch acids include pivalic acid, 2,2-dimethylbutyric acid and 2,2-dimethylpentanoic acid. [1]
It is also possible to realize the kinetic resolution of racemic alcohols by modifying the compositions of the reactants, i.e., by forming MA through reactions between achiral carboxylic acid and the appropriate carboxylic acid anhydride; then, by activating the racemic alcohols using the MA, optically active alcohols and optically active ...