Identify A in the reaction: | vedclass

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(B) The reaction involves the acid-catalyzed hydration of an alkene. $1$. Protonation of the double bond by $H^+$ leads to the formation of a carbocat

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(B) The reaction involves the acid-catalyzed hydration of an alkene. $1$. Protonation of the double bond by $H^+$ leads to the formation of a carbocation. $2$. Due to the strain in the bicyclic system,a ring expansion occurs to form a more stable carbocation. $3$. Water acts as a nucleophile and attacks the carbocation. $4$. Deprotonation yields the final alcohol product,which is a bicyclic alcohol with a methyl and hydroxyl group on adjacent carbons.

Identify $A$ in the reaction:

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