Identify the product A in the following react | vedclass

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(A) The reaction involves the conjugate addition (also known as $1,4$-addition) of an organometallic reagent to an $\alpha,\beta$-unsaturated carbonyl

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$2-$phenylcyclohexanone

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(A) The reaction involves the conjugate addition (also known as $1,4$-addition) of an organometallic reagent to an $\alpha,\beta$-unsaturated carbonyl compound.In the presence of copper salts (like $CuCl$),the Grignard reagent $(PhMgBr)$ forms an organocopper species $(PhCu)$,which acts as a 'soft' nucleophile.Soft nucleophiles prefer to attack the $\beta$-carbon of the $\alpha,\beta$-unsaturated system rather than the carbonyl carbon (which is a 'hard' electrophilic site).Therefore,the phenyl group $(Ph)$ adds to the $\beta$-position of the cyclohexenone ring,followed by protonation $(H^+)$ of the resulting enolate to yield $2$-phenylcyclohexanone.

Identify the product $A$ in the following reaction:
$1$-phenylcyclohex-$1$-en-$1$-one $\xrightarrow[(2) H^+]{(1) PhMgBr/CuCl} (A) (C_{19}H_{20}O)$

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Identify the product $A$ in the following reaction:$1$-phenylcyclohex-$1$-en-$1$-one $\xrightarrow[(2) H^+]{(1) PhMgBr/CuCl} (A) (C_{19}H_{20}O)$