| List-I | List-II | ||
| P. | Cis-2-Butene, trans-2-butene |
1. | Functional isomers |
| Q. | Diethyl ether, Butanol |
2. | Stereoisomers |
| R. | 1-Butene, 2-Butene |
3. | Position isomers |
| S. | n-Pentane, Isopentane |
4. | Chain isomers |
| P | Q | R | S | |
| 1. | 2 | 3 | 4 | 1 |
| 2. | 2 | 1 | 3 | 4 |
| 3. | 3 | 2 | 4 | 1 |
| 4. | 4 | 2 | 1 | 3 |

| (I) | \(\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{Cl} \) |
| (II) | \(\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{OH} \) |
| (III) | ![]() |
| (IV) | ![]() |
| (V) | ![]() |
| 1. | 4 (Four) | 2. | 2 (Two) |
| 3. | 1 (One) | 4. | 8 (Eight) |
| 1. | Seven (7) | 2. | Nine (9) |
| 3. | Six (6) | 4. | Five (5) |
| Statement I: | is optically active. |
| Statement II: | is mirror image of above compound A. |
The absolute configuration of the given compound is :

1. (2R, 3S)
2. (2S, 3R)
3. (2S, 3S)
4. (2R, 3R)
Following types of compounds (as I, II) are studied in terms of isomerism in:
| (I) | CH3CH=CHCH3 |
| (II) |
1. Chain isomerism
2. Position isomerism
3. Conformers
4. Stereisomerism