A molecule (X) with the following structure i | vedclass

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(D) The molecule $(X)$ is an enol ether. Acidic hydrolysis of an enol ether involves the protonation of the double bond followed by the attack of wate

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$A$ and $D$ Only

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(D) The molecule $(X)$ is an enol ether. Acidic hydrolysis of an enol ether involves the protonation of the double bond followed by the attack of water, leading to the cleavage of the $C-O$ bond to produce a carbonyl compound (aldehyde or ketone) and an alcohol.In this specific case, the hydrolysis of the given enol ether yields propanal $(CH_3CH_2CHO)$ and acetone $(CH_3COCH_3)$.$(Y)$ and $(Z)$ are propanal and acetone.Statement $(A)$ is correct as both products have distinct molar masses, but in general, hydrolysis products can be analyzed for mass. Statement $(D)$ is correct because both propanal (an aldehyde) and acetone (a ketone) contain a carbonyl group $(C=O)$, which reacts with $2,4$-dinitrophenylhydrazine $(2,4-DNP)$ to form a hydrazone derivative (addition-elimination reaction).

$A$ molecule $(X)$ with the following structure is hydrolyzed under mild acidic conditions to produce $(Y)$ and $(Z)$. Identify the correct statements about $(Y)$ and $(Z)$.

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