Toluene on reaction with N-Bromosuccinimide gives

1. Phenyl bromomethane

2. o-Bromomethyl benzene

3. p-Bromomethyl benzene

4. m-Bromomethyl benzene

On sulphonation of C₆H₅Cl, the product obtained is-

1. m-Chlorobenzene sulphonic acid is formed

2. Benzene sulphonic acid is formed

3. o-Chlorobenzene sulphonic acid is formed

4. o-and p-Chlorobenzene sulphonic acid is formed

Propene upon heating with \(\mathrm{Cl}_2 \text { at } 500{ }^{\circ} \mathrm{C}\) forms:

Addition of KI accelerates the hydrolysis of primary alkyl halides because:

1. KI is soluble in organic solvents

2. The iodide ion is a weak base and a poor leaving group

3. The iodide ion is a strong base

4. The iodide ion is a powerful nucleophile as well as a good leaving group

$\stackrel{\mathrm{Moist} {\mathrm{Ag}}_2\mathrm{O}}{\to }$ (A) product

Major product (A) is:

1.  

2. 

3. 

4. 

What would be the major product of the given reaction?

1.     

2.    

3.       

4.     

In which reaction product formation does not take place by Hofmann's Rule?

1. $C{H}_3-C{H}_2 - CH-C{H}_3 \underset{∆}{\overset{t-Bu\stackrel{\Theta }{O}\stackrel{\oplus }{K}}{\to }}$
$|$
$Br$

2. $C{H}_3 - C{H}_2 - CH-C{H}_3 \underset{∆}{\overset{C_2{H}_{3}OK}{\to }}$
$|$
$F$

3. ${\mathrm{CH}}_3 - {\mathrm{CH}}_2 - \mathrm{CH}-{\mathrm{CH}}_3 \underset{∆}{\overset{\mathrm{C}{\mathrm{H}}_3\stackrel{-}{\mathrm{O}}\stackrel{+}{\mathrm{K}}}{\to }}$
$|$
$\mathrm{I}$

4. $C{H}_3 - C{H}_2 - CH-\stackrel{\oplus }{N}{\left(C{H}_3\right)}_3{I}^{-} \underset{∆}{\overset{O{H}^{-}}{\to }}$
$|$
$C{H}_3$
$$^-
$$
$$

Which of the following compound would not give an E2 product when treated with sodium ethoxide?

1. 

2. 

3. 

4. 

Product A is

1. 

2. 

3. 

4. 

$\stackrel{NaI/Acetone}{\to }Product$

Which of the following is not a product of the above reaction?

1. 

2. 

3. 

4.