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(C) $HCl$ does not show the peroxide effect (Kharasch effect). The reaction proceeds via Electrophilic Addition Reaction $(EAR)$.$1$. Protonation of t

Vedclass · Accepted Answer

$1-$chloro$-1-$methylcyclohexane

Vedclass · Answer

(C) $HCl$ does not show the peroxide effect (Kharasch effect). The reaction proceeds via Electrophilic Addition Reaction $(EAR)$.$1$. Protonation of the alkene leads to the formation of a more stable carbocation.$2$. The $1$-methylcyclopentyl carbocation undergoes ring expansion to form a more stable $6$-membered ring (cyclohexyl carbocation).$3$. The chloride ion $(Cl^-)$ then attacks the carbocation to form $1$-chloro-$1$-methylcyclohexane as the major product.

$M$ is

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