An organic compound $A$ has the molecular formula $C_3H_6O$ and it undergoes the iodoform test. When saturated with dilute $HCl$,it gives $B$ with the molecular formula $C_9H_{14}O$. $A$ and $B$ respectively are:

Choose the incorrect statement among the following.
$A$. The reactivity of aromatic aldehydes and ketones is less than that of aliphatic carbonyl compounds towards nucleophilic addition reactions.
$B$. Benzaldehyde does not give Fehling's test.
$C$. The $\alpha$-$H$ atoms in ethanal are acidic in nature.
$D$. $p$-nitro benzaldehyde is less reactive than benzaldehyde towards nucleophilic addition reactions.

Product $(A)$ of the reaction is

Cannizzaro reaction between formaldehyde molecules involves the formation of

Which of the following reagents can react with both aldehydes and ketones?

$CaOCl_2 + H_2O \longrightarrow Ca(OH)_2 + X$
$X + CH_3CHO \longrightarrow Y$
$Y + Ca(OH)_2 \longrightarrow CHCl_3$
What is '$Y$'?