The reaction of a carbonyl compound with one of the following reagents involves nucleophilic addition followed by the elimination of water. The reagents are:
1. | A Grignard reagent. |
2. | Hydrazine in the presence of a feebly acidic solution. |
3. | Hydrocyanic acid. |
4. | Sodium hydrogen sulphite. |
Compounds that can exhibit tautomerism, are:
1. l and ll
2. l and lll
3. ll and lll
4. l, ll and lll
The compound among the following that will not be soluble in
sodium hydrogen carbonate is:
1. | 2, 4, 6-Trinitrophenol | 2. | Benzoic acid |
3. | o-Nitrophenol | 4. | Benezenesulphonic acid |
1. | 2. | ||
3. | 4. |
What is the order of the stability of the following tautomeric compounds?
Benzaldehyde cannot be prepared by:
1. | |
2. | |
3. | |
4. |
Predict the products in the given reaction,
1. | 2. | ||
3. | 4. |
Acetone is treated with excess ethanol in the presence of hydrochloric acid.
The product obtained will be:
1. | |
2. | |
3. | |
4. |
The correct order of decreasing acid strength of
trichloroacetic acid (A), trifluoroacetic acid (B), acetic acid (C), and formic acid (D) is:
1. B > A > D > C
2. B > D > C > A
3. A > B > C > D
4. A > C > B >D