Acetophenone,when reacted with a base,C_2H_5O | vedclass

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Question

(C) Acetophenone $(C_6H_5COCH_3)$ contains $\alpha$-hydrogen atoms. When treated with a base like $C_2H_5ONa$,it undergoes an aldol condensation react

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(C) Acetophenone $(C_6H_5COCH_3)$ contains $\alpha$-hydrogen atoms. When treated with a base like $C_2H_5ONa$,it undergoes an aldol condensation reaction. $1$. The base abstracts an $\alpha$-hydrogen to form an enolate ion (nucleophile). $2$. This enolate ion attacks another molecule of acetophenone. $3$. The resulting $\beta$-hydroxy ketone undergoes dehydration upon heating to form an $\alpha, \beta$-unsaturated ketone. $4$. The final product is $4$-phenyl-$4$-phenylbut-$3$-en-$2$-one (or similar structure depending on the specific condensation product),which corresponds to the structure shown in option $C$.

Acetophenone,when reacted with a base,$C_2H_5ONa$,yields a stable compound which has the structure:

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