The suitable product of this reaction is:

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(A) The reaction involves the electrophilic addition of $HF$ to methylenecyclohexane to form a tertiary carbocation intermediate. $1$. Protonation of

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$1-$methyl$-1-$phenylcyclohexane

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(A) The reaction involves the electrophilic addition of $HF$ to methylenecyclohexane to form a tertiary carbocation intermediate. $1$. Protonation of the double bond in methylenecyclohexane by $HF$ generates a stable tertiary carbocation at the $1$-position of the cyclohexane ring. $2$. This tertiary carbocation then acts as an electrophile in a Friedel-Crafts alkylation reaction with benzene. $3$. The benzene ring attacks the carbocation,resulting in the formation of $1$-methyl-$1$-phenylcyclohexane as the final product.

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