$A$ carbonyl compound $X$ $(C_3H_6O)$ on oxidation gives a carboxylic acid $Y$ $(C_3H_6O_2)$. The oxime of $X$ is:

Predict the products in the given reaction.

$A$ $(C_3H_6O)$ $\xrightarrow{NaCN/H_2SO_4}$ cyanohydrin of $A$. If the cyanohydrin is optically active,then the possible structure of $A$ is:

Which of the following can undergo a disproportionation reaction on heating with concentrated alkali?

Which of the following statements are $TRUE$ about Haloform reaction?
$A$. Sodium hypochlorite reacts with $KI$ to give $KOI$.
$B$. $KOI$ is a reducing agent.
$C$. $\alpha, \beta$-unsaturated methylketone will give iodoform reaction.
$D$. Isopropyl alcohol will not give iodoform test.
$E$. Methanoic acid will give positive iodoform test.
Choose the correct answer from the options given below:

The conversion of acetophenone into benzoic acid can be achieved by its reaction with