Acetone reacts with $I_2$ in the presence of $NaOH$ to form:

An organic compound $x$ where the molar ratio of $C$, $O$, and $H$ are equal, on treatment with $50\% \ KOH$ under reflux followed by acidification produced $y$. The most likely structure of $y$ is: [Molar mass of $x$ is $58 \ g \ mol^{-1}$]

$CH_3-CO-CH_3$ $\xrightarrow{NaCN/HCl} A$ $\xrightarrow{H_3O^{+}/\Delta} B$. In the above sequence of reactions,$A$ and $B$ are:

Iodoform test is not given by

Identify the name of the reaction in which the carbonyl group of aldehydes and ketones is reduced to a methylene group upon treatment with hydrazine,followed by heating with sodium hydroxide in ethylene glycol.

Identify $A$ in the following reaction: $A + CH_3MgBr$ $\xrightarrow{\text{ether}} \text{complex}$ $\xrightarrow{H_3O^{+}} (CH_3)_3C-OH$