| Column I | Column II | ||
| a. | ![]() |
i. | Primary amine |
| b. | ![]() |
ii. | Secondary amine |
| c. | \(\mathrm{(C_2H_5)_2CHNH_2}\) | iii. | Tertiary amine |
| d. | \(\mathrm{(C_2H_5)_2NH}\) |
1. a-iii; b-iii; c-i; d-ii
2. a-ii; b-iii c-i; d-ii
3. a-i; b-iii c-i; d-ii
4. a-ii; b-i c-i; d-ii
1. 7
2. 6
3. 8
4. 9
Benzene \(\xrightarrow[conc. HNO_{3}]{conc. H_{2}SO_{4}}\) A \(\xrightarrow[ethanol]{H_{2}, Pd}\) B
B is-
| 1. | Aniline | 2. | Benzene |
| 3. | Cyclohexylamine | 4. | 1-Nitrocyclohexane |
Aniline with excess of methyl iodide in the presence of sodium carbonate solution gives:
1. N, N, N−Trimethylanilinium carbonate.
2. N, N-Dimethylaniline.
3. N, N-Diethylaniline.
4. N, N, N−Triethylanilinium carbonate.