The final product C in the below mentioned reaction is:
\(\xrightarrow[]{Ac_2O}\ A\ \xrightarrow[CH_3COOH]{Br_2}\ B\ \xrightarrow[H^+]{H_2O}\ C\)

1.		2.
3.		4.

Aniline when diazotised in cold and then treated with dimethylaniline, gives a coloured product. Its structure would be :                                                                                 

1.

2. 

3. 

4. 

Aniline in a set of the following reactions yielded a coloured product Y.                        

$\underset{(273-278 \mathrm{K})}{\overset{{\mathrm{NaNO}}_2/\mathrm{HCl}}{\to }}X\stackrel{\mathrm{N},\mathrm{N}- \mathrm{dimethylaniline}}{\to }Y$

The structure of Y would be

1.

2. 

3. 

4. 

What is the end product in the following sequences of operations?

Acetamide$\stackrel{{\mathrm{P}}_2{\mathrm{O}}_5}{\to }\mathrm{A}\stackrel{4\mathrm{H}}{\to }\mathrm{B}$

1. CH₃NH₂                              

2. C₂H₅NH₂

3. CH₃CN                                   

4.  CH₃COONH₄

Name the end product in the following series of reactions,

CH₃COOH $\stackrel{{\mathrm{NH}}_3}{\to }$A$\stackrel{∆}{\to }$B$\stackrel{{\mathrm{P}}_2{\mathrm{O}}_5}{\to }$C:

1. CH₄ 

2. CH₃OH

3. acetonitrile 

4. ammonium acetate

Primary, Secondary and tertiary amines may be separated by using:

1. ethanoyl chlorode

2. diethyl oxalate

3. thionyl chlorode

4. none of these

 are ........... isomers.

1.Chain

2. functional

3. position

4. all of these

Primary nitroalkanes on hydrolysis give:

1. RCOOH + NH₂OH

2. RCOOH

3. NH₂OH

4. RCOR

The numbers of primary amines posible for the formula C₄H₁₁N is -

1. 1

2. 2

3. 3

4. 4

The type of isomerism shown by C₆H₅CN and C₆H₅NC is:

1. Position

2. Functional

3. enantiomer

4. Tautomerism