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(D) The rate of $SN^1$ reaction depends upon the stability of the carbocation intermediate formed in the rate-determining step. $1$. $A$ forms a secon

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$1-$Methyl$-3-$chlorocyclohexene

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(D) The rate of $SN^1$ reaction depends upon the stability of the carbocation intermediate formed in the rate-determining step. $1$. $A$ forms a secondary carbocation. $2$. $B$ forms an allylic secondary carbocation,which is stabilized by resonance. $3$. $C$ forms a tertiary carbocation. $4$. $D$ forms an allylic tertiary carbocation,which is the most stable due to both the tertiary nature and resonance stabilization. Therefore,$D$ is the most reactive for the $SN^1$ reaction.

Which one of the following will be most reactive for $SN^1$ reaction?

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