Methods of Preparation of Amines

How will you convert benzene into $\mathrm{N},\mathrm{N}$-dimethylaniline?

The source of nitrogen in Gabriel synthesis of amines is _____.(Potassium phthalimide/Potassium cyanide)

What is the product $\left(\mathrm{X}\right)$ in the given reaction?

What is the product $\left(\mathrm{X}\right)$ in the given reaction?

Acetanilide on nitration followed by alkaline hydrolysis mainly gives

Which of the following reactions will give a primary amine?

What is the product $\left(\mathrm{X}\right)$ in the given reaction?

The most suitable reagent for the conversion of $2-$phenylpropanamide into $1-$phenylethylamine is:-

Which of the following reagents would not be a good choice for reducing an aryl nitro compound to an amine?

Bromoethane reacts with ${\mathrm{NH}}_3$ to from:

Which one of the following gives secondary amine on reduction:

Ethanamide on Hoffman degradation produces _____.(Methanamine/Ethanamine)

The above reaction is conversion of Nitrobenzene to aniline. It is a _____ reaction for nitrobenzene as oxygen is removed.

Consider the following reaction,

${\mathrm{C}}_2{\mathrm{H}}_5\mathrm{Cl}+\mathrm{AgCN}\stackrel{\mathrm{EtOH}/{\mathrm{H}}_2\mathrm{O}}{⟶}\underset{¯}{\mathrm{X}}$ (major)

Which one of the following statements is true for $\underset{¯}{\mathrm{X}}?$

$\left(\mathrm{I}\right)$ It gives propionic acid on hydrolysis
$\left(\mathrm{II}\right)$ It has an ester functional group
$\left(\mathrm{III}\right)$ It has a nitrogen linked to ethyl carbon
$\left(\mathrm{IV}\right)$ It has a cyanide group

Identify the compound 'B' in the following series of reactions.

Ethanenitrile $\stackrel{\mathrm{Na}/\mathrm{alcohol}}{\to }$A $\stackrel{{\mathrm{NaNO}}_2 /\mathrm{dil}.\mathrm{HCl}}{\to }$B

How many moles of methyl iodide are required to convert ethylamine, diethylamine and triethylamine into quaternary ammonium salt, respectively?

Aromatic amines can be prepared by the reaction of aryl halides with an alcoholic solution of ammonia.