 
| 1. | Bromobenzene | 2. | Benzylbromide | 
| 3. | Acetophenone | 4. | Phenol | 
Identify A and B in the chemical reaction:
| 1. | |
| 2. | |
| 3. | |
| 4. | 
Which of the following compounds will show retention in the configuration on nucleophilic substitution by OH– ion ?
1.
2.
3.
4.
Consider the reaction sequence given below :
The correct statement among the following is:
| 1. | Changing the concentration of base will have no effect on reaction (1) | 
| 2. | Changing the concentration of base will have no effect on reaction (2) | 
| 3. | Changing the base from -OH to -OR will have no effect on reaction (2) | 
| 4. | Doubling the concentration of base will double the rate of both the reactions. | 
The compound form precipitate with aq. AgNO3 solution most readily among the following is-
1. 
2. 
3. 
4. 
Increasing order of reactivity of the following compounds for SN1 substitution is :
1. (A) < (B) < (D) < (C)
2. (B) < (C) < (D) < (A)
3. (B) < (C) < (A) < (D)
4. (B) < (A) < (D) < (C)
What are the major products (A) and (B) for the following reactions, respectively?

| 1. |  | 
| 2. |  | 
| 3. |  | 
| 4. |  | 
The major product (A) of the following reaction is:
| 1. | 2. | ||
| 3. | 4. | 
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. |