Find the correct sequence of the bond enthalpy of the "C-X" bond among the following:
1. CH3-F < CH3-Cl > CH3-Br > CH3-I
2. CH3-Cl > CH3-F > CH3-Br > CH3-I
3. CH3-F < CH3-Cl < CH3-Br < CH3-I
4. CH3-F > CH3-Cl > CH3-Br > CH3-I

Which of the following biphenyls is optically active?
| 1. | 2. | ||
| 3. | 4. |
| 1. | ![]() |
2. | ![]() |
| 3. | \(\mathrm{CH_3CH_2OH}\) | 4. | \(\mathrm{CH_3CH_2Cl}\) |
| 1. | ![]() |
| 2. | ![]() |
| 3. | ![]() |
| 4. | ![]() |
| 1. | (IV) > (III) > (II) > (I) |
| 2. | (I) > (II) > (III) > (IV) |
| 3. | (I) > (III) > (II) > (IV) |
| 4. | (IV) > (II) > (III) > (I) |
The correct reaction among the following is:
| 1. | ![]() |
| 2. | ![]() |
| 3. | ![]() |
| 4. | ![]() |
| 1. | A racemic mixture shows zero optical rotation |
| 2. | SN1 reaction yields a 1:1 mixture of both enantiomers |
| 3. | The product obtained by SN2 reaction of haloalkane having chirality at the reactive site shows the inversion of configuration |
| 4. | Enantiomers are superimposable mirror images on each other |