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 |
The increasing order of the boiling points of the major products A, B and C of the following reactions will be :
(a). | |
(b). | |
(c). |
1. C < A < B
2. B < C < A
3. A < B < C
4. A < C < B
Given below are two statements:
Assertion (A): | Vinyl halides do not undergo nucleophilic substitution easily. |
Reason (R): | Even though the intermediate carbocation is stabilized by loosely held p-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. | Both (A) and (R) are false. |
Wurtz reaction is not preferred for the preparation of alkanes containing an odd number of carbon atoms because:
1. | Boiling points of alkanes obtained in the mixture are very close. |
2. | Melting points of alkanes obtained in the mixture are very close. |
3. | Lattice energy of alkanes obtained in the mixture are very close. |
4. | None of the above. |
1. | Bromobenzene | 2. | Benzylbromide |
3. | Acetophenone | 4. | Phenol |
1. | |
2. | |
3. | |
4. |
1. | These compounds are flammable and highly reactive. |
2. | These are non-toxic organic molecules. |
3. | They are used in refrigerators and air conditioners. |
4. | They are the transporting agents for continuously generating chlorine radicals in stratosphere. |