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(A) The reaction of methylenecyclohexane with $H_3O^+$ proceeds via acid-catalyzed hydration,which follows Markownikoff's rule. The carbocation formed

Vedclass · Accepted Answer

Cyclohexylmethanol ; $1-$methylcyclohexanol

Vedclass · Answer

(A) The reaction of methylenecyclohexane with $H_3O^+$ proceeds via acid-catalyzed hydration,which follows Markownikoff's rule. The carbocation formed at the tertiary carbon is more stable,leading to the formation of $1$-methylcyclohexanol $(Y)$.The reaction with $(i) B_2H_6/THF$ and $(ii) H_2O_2/OH^-$ is hydroboration-oxidation,which follows anti-Markownikoff's rule. The hydroxyl group adds to the less substituted carbon,resulting in the formation of cyclohexylmethanol $(X)$.

$X$ and $Y$ respectively are

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