How many halogen derivatives are possible for ?
1. 2
2. 4
3. 6
4. 9
What is the major product (A) in the following reaction?

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2. | ![]() |
| 3. | ![]() |
4. | ![]() |
Consider the following reaction:

What is the major product A?
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2. | ![]() |
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4. | ![]() |
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
Which of the following compounds will give a racemic mixture on nucleophilic substitution by the OH ion?
| (i) | ![]() |
| (ii) | ![]() |
| (iii) | ![]() |
1. (i)
2. (i), (ii) and (iii)
3. (ii) and (iii)
4. (i) and (iii)
Mark the appropriate reagent used to distinguish vicinal and geminal dihalides.:
| 1. | KOH (aq.) | 2. | KOH(alc.) |
| 3. | Zn dust | 4. | None of these |
Product:
The product of the above mentioned reaction is:
| 1. | ![]() |
2. | ![]() |
| 3. | ![]() |
4. | None of the above |
+ NaI (1 mole) (A); Major product of this reaction is:
1. 
2. 
3. 
4. 
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. |
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. |