(A) | ![]() |
(B) | ![]() |
(C) | ![]() |
(D) | ![]() |
Statement I: | In the Hofmann rearrangement reaction, the alkyl group shifts from a carbonyl carbon atom to the nitrogen atom. |
Statement II: | The tertiary amine formed in Hofman rearrangement reaction contains one carbon less than that present in the original amide. |
1. | Both Statement I & Statement II are true. |
2. | Both Statement I & Statement II are false. |
3. | Statement I is true while Statement II is false. |
4. | Statement I is false while Statement II is true. |
Assertion (A): | In strongly acidic solutions, aniline becomes more reactive towards electrophilic reagents. |
Reason (R): | The amino group being completely protonated in a strongly acidic solution, the lone pair of electrons on the nitrogen is no longer available for resonance |
1. | Both (A) & (R) are True and the reason is the correct explanation of the (A). |
2. | Both (A) & (R) are True but the reason is not the correct explanation of the (A). |
3. | (A) is True but (R) is False. |
4. | (A) is False but (R) is True. |
Amine (List–I) | List - II pKb (aqueous medium) | ||
A. | Aniline | (i) | 9.0 |
B. | Ethanamine | (ii) | 3.29 |
C. | N-Ethylethanamine | (iii) | 3.25 |
D. | N,N-diethylethanamine | (iv) | 3.0 |
A | B | C | D | |
1. | (i) | (ii) | (iv) | (iii) |
2. | (i) | (iv) | (iii) | (ii) |
3. | (i) | (ii) | (iii) | (iv) |
4. | (ii) | (iii) | (iv) | (i) |
The most reactive amine towards dilute hydrochloric acid is:
1. | ![]() |
2. | ![]() |
3. | ![]() |
4. | ![]() |
1. | ![]() |
2. | ![]() |
3. | ![]() |
4. | ![]() |
Assertion (A): | p-Toluidine is a stronger base than m-toluidine. |
Reason (R): | The methyl group from m-position exerts a smaller electron-donating inductive (+l) effect than from p-position. |
1. | Both (A) and (R) are True and (R) is the correct explanation for (A). |
2. | Both (A) and (R) are True but (R) is not the correct explanation for (A). |
3. | (A) is True but (R) is False. |
4. | Both (A) and (R) are False. |
Which of the following should be most volatile?
I. | \(\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{CH}_2 \mathrm{NH}_2\) |
II. | \(\left(\mathrm{CH}_3\right)_3 \mathrm{~N}\) |
III. | ![]() |
IV. | \(\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{CH}_3\) |
1. | II | 2. | IV |
3. | I | 4. | III |
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3. | ![]() |
4. | ![]() |