The compound obtained when acetaldehyde reacts with dilute aqueous sodium hydroxide exhibits

Predict the product $X$ for the following reaction:
$2\text{-oxocyclohex-3-en-1-yl} \text{ acetate derivative} \rightarrow{NaBH_4, MeOH} X$

What will be the product $B$ in the following sequence of reactions?
$HC \equiv CH$ $\xrightarrow{30\% \, H_2SO_4, \, HgSO_4} A$ $\xrightarrow{NaOH} B$

An organic compound $(X)$ with molecular formula $C_3H_6O$ is not readily oxidised. On reduction it gives $(C_3H_8O)$ $(Y)$ which reacts with $HBr$ to give a bromide $(Z)$ which is converted to a Grignard reagent. This Grignard reagent on reaction with $(X)$ followed by hydrolysis gives $2,3-$dimethylbutan$-2-$ol. Compounds $(X)$,$(Y)$ and $(Z)$ respectively are $:$

The order of susceptibility of nucleophilic attack on aldehydes follows the order:

The product formed when hydroxylamine $(NH_2OH)$ condenses with a carbonyl compound is called: