What will be the product in the following rea | vedclass

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(A) The reaction proceeds via an $S_N1$ mechanism.$1$. The leaving group $Cl^-$ departs to form a tertiary $(3^{\circ})$ carbocation at the $1$-positi

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$1-$methylcyclohexanol

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(A) The reaction proceeds via an $S_N1$ mechanism.$1$. The leaving group $Cl^-$ departs to form a tertiary $(3^{\circ})$ carbocation at the $1$-position of the cyclohexane ring.$2$. This $3^{\circ}$ carbocation is already stable and does not undergo rearrangement.$3$. Water $(H_2O)$ acts as a nucleophile and attacks the carbocation.$4$. Subsequent deprotonation yields $1$-methylcyclohexanol as the final product.

What will be the product in the following reaction?
$1$-chloro-$1$-methylcyclohexane $\xrightarrow{H_2O}$ ?

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What will be the product in the following reaction?$1$-chloro-$1$-methylcyclohexane $\xrightarrow{H_2O}$ ?