Arrange the following in the order of C-Br bond strength in a polar solvent
1. I<II<III<IV
2. III<IV<I<II
3. IV<III<II<I
4. II<I<III<IV
What is the correct order of reactivity for the following compounds in an \(S_N 1\) reaction?
1. | II > I > III | 2. | III > II > I |
3. | I > II > III | 4. | I > III > II |
1. | Bromobenzene | 2. | Benzylbromide |
3. | Acetophenone | 4. | Phenol |
Which of the following compounds will give racemic mixture on nucleophilic substitution by OH ion?
(i) | |
(ii) | |
(iii) |
1. (iii)
2. (i), (ii) and (iii)
3. (ii) and (iii)
4. (i) and (iii)
How many unique substitution products can be formed when ethane reacts with bromine under sunlight?
1. | 9 | 2. | 6 |
3. | 8 | 4. | 5 |
1. | |
2. | |
3. | |
4. |
Assertion (A): | Vinyl halides do not undergo nucleophilic substitution easily. |
Reason (R): |
Even though the intermediate carbocation is stabilized by loosely held \(\pi-\)electrons, the cleavage is difficult because of strong bonding.
|
1. | Both (A) and (R) are True and (R) is the correct explanation of (A). |
2. | Both (A) and (R) are True but (R) is not the correct explanation of (A). |
3. | (A) is True but (R) is False. |
4. | (A) is False but (R) is True. |