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(A) The reaction is an acid-catalyzed hydration of an alkene. $1$. The proton $(H^+)$ attacks the double bond to form the most stable carbocation inte

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$I$

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(A) The reaction is an acid-catalyzed hydration of an alkene. $1$. The proton $(H^+)$ attacks the double bond to form the most stable carbocation intermediate. $2$. The protonation of the alkene leads to a tertiary carbocation at the carbon attached to the cyclohexyl group. $3$. Water $(H_2O)$ then acts as a nucleophile and attacks this tertiary carbocation. $4$. Subsequent deprotonation yields the tertiary alcohol as the major product,which corresponds to structure $I$.

What is the major product of the following reaction?

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