$C_{7}H_{10}O$ reacts with $CH_{3}MgBr$ to give a compound $C_{8}H_{12}O$ which gives a positive iodoform test. Identify the structure of $A$.

The product formed by the reaction of an aldehyde with a primary amine is

Which of the following does not give Fehling solution test?

Given below are the four isomeric compounds $(P, Q, R, S)$. Identify the correct statements from below.
$A$. $Q, R$ and $S$ will give a precipitate with $2,4-DNP$.
$B$. $P$ and $Q$ will give a positive Bayer's test.
$C$. $Q$ and $R$ will give a sooty flame.
$D$. $R$ and $S$ will give a yellow precipitate with $I_2/NaOH$.
$E$. $Q$ alone will deposit silver with Tollen's reagent.
Choose the correct option.

The major product formed in the following reaction sequence is $CH_3-CH=CH_2$ $\xrightarrow[\substack{(iii) \ CH_3-CH_2-CHO \\ (iv) \ CrO_3}]{\substack{(i) \ HBr, \text{ peroxide} \\ (ii) \ Mg}}$

Benzaldehyde can be converted to benzonitrile by treatment with