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(C) Step $1$: Dehydration of cyclohexylmethanol using $H_3PO_4$ at $120^{\circ}C$ proceeds via an $E1$ mechanism to form the more stable alkene,$1$-me

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$2-$Methylcyclohexanol

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(C) Step $1$: Dehydration of cyclohexylmethanol using $H_3PO_4$ at $120^{\circ}C$ proceeds via an $E1$ mechanism to form the more stable alkene,$1$-methylcyclohexene,as the major product $A$.Step $2$: Hydroboration-oxidation $(HBO)$ of $1$-methylcyclohexene involves the anti-Markovnikov addition of water across the double bond.The $OH$ group attaches to the less hindered carbon atom (the $CH$ group of the double bond),while the $H$ atom attaches to the more hindered carbon atom (the $C-CH_3$ group).Therefore,the final major product $P$ is $2$-methylcyclohexanol.

Consider the above reaction and identify the product $P :$

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