Embibe Experts Solutions for Chapter: Amines, Exercise 2: Exercise 2

Starting from propanoic acid, the following reactions were carried out: Propanoic acid $\stackrel{{\mathrm{SOCl}}_2}{⟶}\mathrm{X}\stackrel{{\mathrm{NH}}_3}{⟶}\mathrm{Y}\stackrel{{\mathrm{Br}}_2+\mathrm{KOH}}{⟶}\mathrm{Z}$. What is the compound $\mathrm{Z}$?

Aniline when acetylated, the product on nitration followed by alkaline hydrolysis gives:

An aromatic amine $\left(\mathrm{X}\right)$ was treated with alcoholic potash and another compound $\left(\mathrm{Y}\right)$, then the foul smelling gas ${\mathrm{C}}_6{\mathrm{H}}_5\mathrm{NC}$ is formed. The compound $\left(\mathrm{Y}\right)$ was formed by reacting compound $\left(\mathrm{Z}\right)$ with ${\mathrm{Cl}}_2$ in the presence of slaked lime. The compound $\left(\mathrm{Z}\right)$ is:

$\mathrm{p}$ -chloroaniline and anilinium hydrogen chloride can be distinguished by

In the diazotisation of aniline with sodium nitrite and hydrochloric acid, an excess of hydrochloric acid is used primarily to

An organic compound with the molecular formula ${\mathrm{C}}_3{\mathrm{H}}_5 \mathrm{N}$ on hydrolysis forms an acid which reduces Fehling's solution. The compound can be ____________

Which of the following gives a primary amine on reduction?

Correct basic strength order is: