Identify the major product P in the following | vedclass

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(A) The reaction proceeds through the following steps:$1$. The base $HO^-$ abstracts an $\alpha$-hydrogen from $1,3-	ext{cyclohexanedione}$ to form a

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(A) The reaction proceeds through the following steps:$1$. The base $HO^-$ abstracts an $\alpha$-hydrogen from $1,3-	ext{cyclohexanedione}$ to form an enolate ion.$2$. This enolate ion performs a nucleophilic substitution $(S_N2)$ on $Cl-CH_2-CHO$,displacing the chloride ion.$3$. The resulting intermediate undergoes an intramolecular aldol condensation followed by dehydration to form the final bicyclic product.$4$. The final product is a fused ring system containing a ketone and a furan ring,which corresponds to option $A$.

Identify the major product $P$ in the following reaction:
$1,3-\text{cyclohexanedione} + Cl-CH_2-CHO \xrightarrow{\text{aq. NaOH}} P$

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Identify the major product $P$ in the following reaction:$1,3-\text{cyclohexanedione} + Cl-CH_2-CHO \xrightarrow{\text{aq. NaOH}} P$