CH₃CH₂Cl$\stackrel{\mathrm{NaCN}}{\to }$X$\stackrel{\mathrm{Ni}/{\mathrm{H}}_2}{\to }$Y$\stackrel{\mathrm{Acetic}<mspace\; width="1em"></mspace>\mathrm{anhydride}}{\to }$Z

In the above reaction sequence, Z is                                  

1. CH₃CH₂CH₂NHCOCH₃

2. CH₃CH₂CH₂NH₂

3. CH₃CH₂CH₂CONHCH₃

4. CH₃CH₂CH₂CONHCOCH₃

Aniline in a set of reactions yield the following products                                                   

The structure of the product D would be -

1. C₆H₅CH₂NH₂

2. C₆H₅NHCH₂CH₃

3. C₆H₅NHOH

4. C₆H₅CH₂OH

Product Q in the above reaction is             

1.
2.
3.
4.

Which one of the following on reduction with LiAlH₄ yields a secondary amine ?

[2007]

1. Methyl isocyanide

2. Acetamide

3. Methyl cyanide

4. Nitroethane

In the reaction,

${\mathrm{CH}}_3\mathrm{CN}+2\mathrm{H}\underset{{\mathrm{SnCl}}_2}{\overset{\mathrm{HCl}}{\to }}X<mspace\; width="1em"></mspace>\stackrel{\mathrm{Boiling}<mspace\; width="1em"></mspace>{\mathrm{H}}_2\mathrm{O}}{\to }<mspace\; width="1em"></mspace>Y,$ the term Y is 

[1999]

1. Acetone

2. Ethanamine

3. Acetaldehyde

4. Dimethyl amine

RMgX on reacting with cyanogen chloride gives:

1. R-NC

2. R-Cl

3. R-CN

4. None of the above

The compound obtained by heating a mixture of primary amine and chloroform with ethanolic potassium hydroxide (KOH) is

[1997]

1. An alkyl isocyanide

2. An alkyl halide

3. An amide

4. An amide and nitro compound

Alkyl halide (RX) on treatment with KCN followed by reduction leads to the formation of:

1. RNH₂

2. RCH₂NH₂

3. RH + NH₃

4. RCH₃ + N₂

Dehydration of an amide gives:

1. Cyanide

2. Amine

3. Isocyanide

4. Fatty acid

The compound A and B respectively are:

1.		2.
3.		4.