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

1.	\(\mathrm{CH}_3-\mathrm{CHCl}-\mathrm{CH}_2 \mathrm{Cl} \)	2.	\(\mathrm{CH}_2 \mathrm{Cl}-\mathrm{CH}=\mathrm{CH}_2 \)
3.	\(\mathrm{CH}_2 \mathrm{Cl}-\mathrm{CHCl}-\mathrm{CH}_2 \mathrm{Cl} \)	4.	All of the above

 Which of the following products are formed on sulphonation of chlorobenzene(C₆H₅Cl)?

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

Toluene on reaction with N-Bromosuccinimide gives

1. Phenyl bromomethane

2. o-Bromomethyl benzene

3. p-Bromomethyl benzene

4. m-Bromomethyl benzene

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

$\stackrel{\mathrm{Moist}<mspace\; width="1em"></mspace>{\mathrm{Ag}}_2\mathrm{O}}{\to }$ (A) product

Major product (A) is:

1.  

2. 

3. 

4. 

What would be the major product of the given reaction?

1.     

2.    

3.       

4.     

Which of the following reactions does not follow
Hofmann's rule in the formation of the major alkene product?

1.
2.
3.
4.

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.