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Electrical EngineeringQ&A LibraryThe base-promoted rearrangement of an a-haloketone to a carboxylic acid, known as the Favorskii rearrangement, is illustrated by the conversion of 2-chlorocyclohexanone to cyclopentanecarboxylic acid. CI CO Na+ COH NaOH NaOH HCI THF THF H,O A proposed intermediate It is proposed that NaOH first converts the a-haloketone to the substituted cyclopropa- none shown in brackets and then to the sodium salt of cyclopentanecarboxylic acid.Start your trial now! First week only $4.99!*arrow_forward*

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Propose a mechanism for base-promoted conversion of 2-chlorocyclohexanone to the proposed intermediate.

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