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(A) The reaction involves the acid-catalyzed dehydration of $cis-4-methylcyclohexanol$ using $H^+$ and heat $(\Delta)$.This process proceeds via an $E

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Racemic

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(A) The reaction involves the acid-catalyzed dehydration of $cis-4-methylcyclohexanol$ using $H^+$ and heat $(\Delta)$.This process proceeds via an $E1$ mechanism involving the formation of a carbocation intermediate.The dehydration leads to the formation of $4-methylcyclohexene$.Since the product $4-methylcyclohexene$ has a chiral center at the $C4$ position,the reaction produces a pair of enantiomers in equal amounts,which is known as a racemic mixture.

The products obtained in the following reaction are:

Similar Questions

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