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Cyclopentanecarboxylic acid is an organic compound with the formula C 5 H 9 CO 2 H. It is a colorless nonvolatile oil. It is a colorless nonvolatile oil. It can be produced by the palladium -catalyzed hydrocarboxylation of cyclopentene : [ 2 ]
The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.
Palladium-catalyzed hydrocarboxylation of cyclopentene gives cyclopentanecarboxylic acid: [8] C 5 H 8 + CO + H 2 O → C 5 H 9 CO 2 H. References
Cyclohexanecarboxylic acid is a precursor to the nylon-6 precursor caprolactam via its reaction with nitrosylsulfuric acid. It can also be oxidized to cyclohexene. [2] Cyclohexanecarboxylic acid exhibits the reactions typical of carboxylic acids, including its conversion to the acid chloride cyclohexanecarbonyl chloride. [3] [4]
The Favorskii rearrangement is principally a rearrangement of cyclopropanones and α-halo ketones that leads to carboxylic acid derivatives. In the case of cyclic α-halo ketones, the Favorskii rearrangement constitutes a ring contraction.
C. Calconcarboxylic acid; Candesartan; Candoxatril; Canrenoic acid; Captopril; Carbenzide; Carbestrol; Carbonic acid; Carboxyatractyloside; 9-Carboxymethoxymethylguanine
Cyclopentanecarboxylic acid; Ethyl methacrylate; Hexane-2,5-dione (2R)-2-Methylpent-4-enoic acid This page was last edited on 31 January 2024, at 01:00 ...
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