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(C) The reaction proceeds as follows:$1$. The first step is the anti-Markovnikov addition of $HBr$ to methylenecyclohexane in the presence of a peroxi

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Cyclohexylacetic acid.

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(C) The reaction proceeds as follows:$1$. The first step is the anti-Markovnikov addition of $HBr$ to methylenecyclohexane in the presence of a peroxide,$(C_6H_5CO)_2O_2$. This yields (cyclohexylmethyl) bromide,$C_6H_{11}CH_2Br$.$2$. The second step is a nucleophilic substitution reaction with $KCN$,where the bromide ion is replaced by a cyanide group,yielding cyclohexylacetonitrile,$C_6H_{11}CH_2CN$.$3$. The third step is the acid-catalyzed hydrolysis of the nitrile group followed by heating,which converts the $-CN$ group into a carboxylic acid group,$-COOH$. The final product is cyclohexylacetic acid,$C_6H_{11}CH_2COOH$.

The major product in the following reaction is:

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