When CH₃CH₂CHCl₂ is treated with NaNH₂, the product formed is:                             

1. CH₃-CH=CH₂ 

2. CH₃-C$\equiv$CH

3. CH₃CH₂CH${<}_{{\mathrm{NH}}_2}^{{\mathrm{NH}}_2}$   

4. CH₃CH₂C${<}_{{\mathrm{NH}}_2}^{\mathrm{Cl}}$

Chlorobenzene reacts with Mg in dry ether to give a compound (A).
A and ethanol continue to react in order to produce?

R-CH₂-CCl₂-R $\stackrel{\mathrm{Reagent}}{\to }$R-C$\equiv$C-R. The reagent is

1. Na

2. HCl in H₂O

3. KOH in C₂H₅OH

4. Zn in alcohol

Ethyl chloride is converted into diethyl ether by -                                                  

 1. Wurtz reaction                           
 2. Grignard reaction
 3. Perkin's reaction                       
 4. Williamson's synthesis

The alkyl halide is converted into an alcohol by:                                    

What is produced when Br₂ is added to cis-but-2-ene?

1. Racemic mixture of 2,3-Dibromobutane

2. Meso form of 2,3-Dibromobutane

3. Dextro form of 2,3-Dibromobutane

4. Laevo form of 2,3-Dibromobutane 

When ethane and bromine are allowed to interact in sunlight, how many distinct substitution products are possible?

 , Cl obtained by chlorination of n-butane, will be                

1. meso form              

2. racemic mixture

3. d-form                 

4. l-form

The reactivity order of halides for dehydrohalogenation is 

1. R-F>R-Cl>R-Br>R-I

2. R-I>R-Br>R-Cl>R-F

3. R-I>R-Cl>R-Br>R-F

4.  R-F>R-I>R-Br>R-Cl

In ${\mathrm{S}}_{{\mathrm{N}}^2}$ reactions, the correct order of reactivity for the following compounds : ${\mathrm{CH}}_3\mathrm{Cl}$, ${\mathrm{CH}}_3{\mathrm{CH}}_2\mathrm{Cl}$, ${\left({\mathrm{CH}}_3\right)}_2\mathrm{CHCl}$ and ${\left({\mathrm{CH}}_3\right)}_3\mathrm{CCl}$ is :

1. ${\mathrm{CH}}_3\mathrm{Cl}$>${\left({\mathrm{CH}}_3\right)}_2\mathrm{CHCl}$>${\mathrm{CH}}_3{\mathrm{CH}}_2\mathrm{Cl}$>${\left({\mathrm{CH}}_3\right)}_3\mathrm{CCl}$

2. ${\mathrm{CH}}_3\mathrm{Cl}$>${\mathrm{CH}}_3{\mathrm{CH}}_2\mathrm{Cl}$>${\left({\mathrm{CH}}_3\right)}_2\mathrm{CHCl}$>${\left({\mathrm{CH}}_3\right)}_3\mathrm{CCl}$

3. ${\mathrm{CH}}_3{\mathrm{CH}}_2\mathrm{Cl}$>${\mathrm{CH}}_3\mathrm{Cl}$>${\left({\mathrm{CH}}_3\right)}_2\mathrm{CHCl}$>${\left({\mathrm{CH}}_3\right)}_3\mathrm{CCl}$

4. ${\left({\mathrm{CH}}_3\right)}_2\mathrm{CHCl}$>${\mathrm{CH}}_3{\mathrm{CH}}_2\mathrm{Cl}$>${\mathrm{CH}}_3\mathrm{Cl}$>${\left({\mathrm{CH}}_3\right)}_3\mathrm{CCl}$