The below structure is an example of :

| 1. | Cyanohydrin | 2. | Hemiacetal |
| 3. | Acetal | 4. | Cyanoalcohol |
The structure of Hex-2-en-4-ynoic acid is:
| 1. | ![]() |
| 2. | ![]() |
| 3. | ![]() |
| 4. | None of these |
The major product formed when cyclohexanecarbaldehyde reacts with PhMgBr and H3O+ is:
| 1. | 2. | ||
| 3. | 4. | None of these |
What is the major product of the reaction between cyclohexanecarbaldehyde and Tollens' reagent?
| 1. | 2. | ||
| 3. | 4. | None of these |
The compounds that undergoes the Cannizzaro reaction are:
(i) Methanal
(ii) 2-Methylpentanal
(iii) Benzaldehyde
(iv) Benzophenone
1. (i)
2. (ii)
3. (i), (iii)
4. (i), (ii), (iii)
Propanal and butanal can produce four different aldol condensation products. The possible structure is/are:
| 1. | ![]() |
| 2. | ![]() |
| 3. | Both (1) and (2) |
| 4. | None of the above |
An organic compound with the molecular formula C9H10O forms a 2,4-DNP derivative, reduces Tollens’ reagent, and undergoes the Cannizzaro reaction. On vigorous oxidation, it gives 1,2-benzenedicarboxylic acid. This organic compound will be:
| 1. | 2-Methyl benzaldehyde | 2. | 2-Hydroxy benzaldehyde |
| 3. | 2-Ethyl benzaldehyde | 4. | 4-Ethyl benzaldehyde |
Organic compound (A), having molecular formula C₈H₁₆O₂, on hydrolysis with dilute H₂SO₄ gives a carboxylic acid (B) and an alcohol (C). Oxidation of alcohol (C) with chromic acid gives the same carboxylic acid (B). On dehydration, alcohol (C)
gives but-1-ene.
Identify compound (B).
| 1. | Butanoic acid | 2. | Propanoic acid |
| 3. | Butanol | 4. | Pentanoic acid |