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 |
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
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
(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 Hoffmann's Rule?
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Which of the following compound would not give an E2 product when treated with sodium ethoxide?
1.
2.
3.
4.
Which of the following is not a product of the above reaction?
1.
2.
3.
4.