What is the product of the following reaction | vedclass

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(B) The reaction proceeds in two main steps:$1$. Epoxidation: Cyclohexene reacts with a peroxyacid $(RCO_3H)$ to form cyclohexene oxide (an epoxide).$

Vedclass · Accepted Answer

$2-$methylcyclohexanol (trans-isomer)

Vedclass · Answer

(B) The reaction proceeds in two main steps:$1$. Epoxidation: Cyclohexene reacts with a peroxyacid $(RCO_3H)$ to form cyclohexene oxide (an epoxide).$2$. Nucleophilic Ring Opening: The Grignard reagent $(CH_3MgBr)$ acts as a nucleophile $(CH_3^-)$ and attacks the epoxide ring. The attack occurs from the side opposite to the oxygen atom,leading to an anti-addition.$3$. Protonation: Subsequent treatment with $H_3O^+$ protonates the alkoxide to form the alcohol.$4$. Stereochemistry: The $CH_3$ group and the $OH$ group are added in a trans-configuration relative to each other. Thus,the product is trans$-2-$methylcyclohexanol.

What is the product of the following reaction?

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