The esters that get hydrolyzed most easily under alkaline conditions is?
| 1. | ![]() |
| 2. | ![]() |
| 3. | ![]() |
| 4. | ![]() |
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. | ![]() |