Vinylcyclopentane xrightarrow{HCl} Major prod | vedclass

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(A) The reaction proceeds via the formation of a carbocation intermediate. $1$. Protonation of the alkene gives a secondary carbocation on the side ch

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$1-$chloro$-1-$methylcyclohexane

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(A) The reaction proceeds via the formation of a carbocation intermediate. $1$. Protonation of the alkene gives a secondary carbocation on the side chain. $2$. The five-membered ring undergoes ring expansion to form a more stable six-membered ring carbocation. $3$. $A$ $1,2$-hydride shift occurs to form a more stable tertiary carbocation. $4$. Finally,the chloride ion attacks the tertiary carbocation to form $1$-chloro-$1$-methylcyclohexane.

Vinylcyclopentane $\xrightarrow{HCl}$ Major product is

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