Which of the following statements about the conformers of ethane is correct?”
| 1. | Bond angle changes, but bond length remains the same. |
| 2. | Both bond angle and bond length change. |
| 3. | Both bond angle and bond length remain the same. |
| 4. | Bond angle remains the same, but the bond length changes. |
The correct order with respect to –I effect of the substituents is:
(R = alkyl)
1. –NH2 > –OR < –F
2. –NR2 < –OR < –F
3. –NH2 > –OR > –F
4. –NR2 > –OR > –F
The most stable carbocation among the following is:
| 1. | ` |
2. | ![]() |
| 3. | ![]() |
4. | ![]() |
The correct statement about the SN1 reaction is:
| 1. | 100 % racemisation. |
| 2. | Inversion more than retention leads to partial racemisation. |
| 3. | 100 % retention. |
| 4. | 100 % Inversion. |
Which one of the following statements is not correct for a nucleophile?
1. Nucleophile is a lewis acid.
2. Ammonia is a nucleophile.
3. Nucleophiles attack low electron density sites.
4. Nucleophiles are not electron-seeking.
Two possible stereo-structures of CH3CHOH.COOH, that are optically active, called:
| 1. | Diastereomers | 2. | Atropisomers |
| 3. | Enantiomers | 4. | Mesomers |
In Duma's method for estimation of nitrogen, 0.25 g of an organic compound gave 40 mL of nitrogen collected at 300 K temperature and 725 mm pressure. If the aqueous tension at 300 K is 25 mm, the percentage of nitrogen in the compound is:
| 1. | 17.36 | 2. | 18.20 |
| 3. | 16.76 | 4. | 15.76 |
Which of the following compounds gives the most stable carbocation on ionization of its C–Cl bond?
| 1. | ![]() |
2. | ![]() |
| 3. | ![]() |
4. | ![]() |
Hyperconjugation occurs among the following compounds:

| 1. | I only | 2. | II only |
| 3. | III only | 4. | I and III |
The enolic form of ethyl acetoacetate is given below:

The number of σ and π bonds in the enolic form are respectively:
1. 18 sigma bonds and 2 pi-bonds
2. 16 sigma bonds and 1 pi-bond
3. 9 sigma bonds and 2 pi-bonds
4. 9 sigma bonds and 1 pi-bond