Which of the following best describes the nucleophilic addition step in the acid-catalyzed hydrolysis of acetonitrile $(CH_3CN)$?

What are $X$ and $Y$ respectively in the following reactions?

Considering the reaction sequence given below,the correct statement$(s)$ is(are):
$A$. $P$ can be reduced to a primary alcohol using $NaBH_4$.
$B$. Treating $P$ with conc. $NH_4OH$ solution followed by acidification gives $Q$.
$C$. Treating $Q$ with a solution of $NaNO_2$ in aq. $HCl$ liberates $N_2$.
$D$. $P$ is more acidic than $CH_3CH_2COOH$.

The product $(A)$ of the reaction is:

The reaction sequence is:
$2-\text{hydroxycyclohexylacetone}$ $\xrightarrow{I_2/NaOH}$ $\xrightarrow{\Delta}$ $\xrightarrow{H^+}$ $\xrightarrow{\Delta} A$
$A$ is:

In the following reaction,$X$ and $Y$ are respectively
$CH_3 COOH + NH_3$ $\longrightarrow X \stackrel{\Delta}{}$ ${\longrightarrow} Y + H_2 O$