Which haloarenes is most reactive towards electrophilic substitution reaction?

1.		2.
3.		4.

Which nitro derivative of haloarene is most reactive towards nucleophilic substitution reaction?

1. 

 2.

 3. 

4.

End product D of the following reaction will be

(1)
(2)
(3)
(4)

 $\stackrel{\mathrm{Na}/\mathrm{Dry} \mathrm{ether}}{\to }$ (A)

                                                       97%

Product (A) of above reaction is:

1.  

2.  

3.  

4.  

Which hydrogen can the Br radical abstract the most easily?

1. a

2. b

3. c

4. d

Product obtained in above Wurtz reaction is:-
$\stackrel{Na(Dry ether)}{\to }$

(1) 

(2)
(3)        

(4) Both (1) and (2)

$\mathrm{Cl}-{\mathrm{CH}}_2-\underset{{\mathrm{CH}}_3}{\overset{{\mathrm{CH}}_3}{\underset{\left|}{\overset{\right|}{\mathrm{C}}}}}-{\mathrm{CH}}_2-{\mathrm{CH}}_2-\mathrm{Cl}+{\mathrm{I}}^{-} ---> \mathrm{Product}$
The major product of the above reaction is:-

1.$\mathrm{I}-{\mathrm{CH}}_2-\underset{{\mathrm{CH}}_3}{\overset{{\mathrm{CH}}_3}{\underset{\left|}{\overset{\right|}{\mathrm{C}}}}}-{\mathrm{CH}}_2-{\mathrm{CH}}_2-\mathrm{Cl}$

2. $\mathrm{Cl}-{\mathrm{CH}}_2-\underset{{\mathrm{CH}}_3}{\overset{{\mathrm{CH}}_3}{\underset{\left|}{\overset{\right|}{\mathrm{C}}}}}-{\mathrm{CH}}_2-{\mathrm{CH}}_2-\mathrm{I}$

3. ${\mathrm{H}}_2\mathrm{C}=\stackrel{{\mathrm{CH}}_3}{\stackrel{|}{\mathrm{C}}}-{\mathrm{CH}}_2-{\mathrm{CH}}_2=\mathrm{Cl}$

4. $\mathrm{Cl}-{\mathrm{CH}}_2-\underset{{\mathrm{CH}}_3}{\overset{{\mathrm{CH}}_3}{\underset{\left|}{\overset{\right|}{\mathrm{C}}}}}-{\mathrm{CH}}_2={\mathrm{CH}}_2$

+ NaI (1 mole) $\stackrel{\mathrm{Acetone}}{\to }$(A); Major product of this reaction is:

1. 

2. 

3. 

4. 

Which of the following alkyl halide undergo rearrangement in S_N1 reaction?

1. $\begin{array}{ccccccc}{\mathrm{CH}}_3& -& \underset{{\mathrm{CH}}_3}{\underset{|}{\stackrel{{\mathrm{CH}}_3}{\stackrel{|}{\mathrm{C}}}}}& -& \underset{\mathrm{I}}{\underset{|}{\mathrm{CH}}}& -& {\mathrm{CH}}_3\end{array}$

2.  

3.  

4. All of these