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(B) The reaction of an alkene with a peroxyacid (like $mCPBA$) followed by acid-catalyzed hydrolysis $(H_3O^+)$ is a two-step process that results in

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$1,2-$dimethylcyclopentane$-1,2-$diol (trans-isomer)

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(B) The reaction of an alkene with a peroxyacid (like $mCPBA$) followed by acid-catalyzed hydrolysis $(H_3O^+)$ is a two-step process that results in anti-dihydroxylation.$1$. The alkene reacts with $mCPBA$ to form an epoxide.$2$. The epoxide undergoes acid-catalyzed ring opening by water,which proceeds via an $S_N2$-like mechanism,leading to the anti-addition of two hydroxyl groups.For $1,2-dimethylcyclopent-1-ene$,this results in the formation of the trans$-1,2-$dimethylcyclopentane$-1,2-$diol.

Choose the correct product of the following reaction:
$1$,$2$-dimethylcyclopent$-1-$ene $\xrightarrow[2. H_3O^+]{1. mCPBA}$ Product

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Choose the correct product of the following reaction:$1$,$2$-dimethylcyclopent$-1-$ene $\xrightarrow[2. H_3O^+]{1. mCPBA}$ Product