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 $x$?

When a nucleophile encounters a ketone,the site of attack is

The major product formed in the following reaction is:

Considering the following reaction sequence,the correct statement$(s)$ is(are):
$A$. Compounds $P$ and $Q$ are carboxylic acids.
$B$. Compound $S$ decolorizes bromine water.
$C$. Compounds $P$ and $S$ react with hydroxylamine to give the corresponding oximes.
$D$. Compound $R$ reacts with dialkylcadmium to give the corresponding tertiary alcohol.

Which of the following compounds,upon hydrolysis followed by heating,gives a product that yields a positive iodoform test?

Which of the following substances cannot be used as a starting material for the preparation of iodoform?