Predict the product (A) of the following reac | vedclass

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(A) The reaction proceeds via the following steps:$1$. Protonation of the alkene to form a stable $3^{\circ}$ carbocation.$2$. Ring expansion of the c

Vedclass · Accepted Answer

$1,2-$dimethylcyclohex$-1-$ene

Vedclass · Answer

(A) The reaction proceeds via the following steps:$1$. Protonation of the alkene to form a stable $3^{\circ}$ carbocation.$2$. Ring expansion of the cyclobutane ring to a more stable cyclohexane ring.$3$. $A$ $1,2$-methyl shift to form a more stable tertiary carbocation.$4$. Deprotonation to form the most stable alkene,which is $1,2$-dimethylcyclohex-$1$-ene.

Predict the product $(A)$ of the following reaction:

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