The aldol condensation product of acetone on dehydration gives:

Aldol condensation will not take place in

$A$ in the given reaction is

Compound $x$ having molecular formula $C_3H_6O$ is reduced by Red $P/HI$ to give compound $y$ $(C_3H_8)$. Since $x$ reduces Tollen's reagent,what is the possible structure of $x$?

An organic compound contains $69.77 \%$ carbon,$11.63 \%$ hydrogen and the rest is oxygen. The molecular mass of the compound is $86$. It does not reduce Tollens' reagent but forms an addition compound with sodium hydrogensulphite and gives a positive iodoform test. On vigorous oxidation,it gives ethanoic acid and propanoic acid. Write the possible structure of the compound.

The product $(P)$ formed in the following reaction is $:$