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 |
For the following substrates, the characteristic aldol condensation occurs with?
i) Methanal (ii) 2-Methylpentanal (iii) Benzaldehyde
(iv) Benzophenone (v) Cyclohexanone (vi) 1-Phenylpropanone
(vii) Phenylacetaldehyde (viii) Butan-1-ol (ix) 2,2-Dimethylbutanal
1. (ii), (v), (vi), (vii)
2. (iii) & (iv)
3. all of the above
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 structures are:
1. | ![]() |
2. | ![]() |
3. | Both (1) and (2) |
4. | None of these |
1. Low electrophilicity in 2,2,6-trimethylcyclohexanone
2. Less steric crowd in 2,2,6-trimethylcyclohexanone
3. More steric crowd in 2,2,6-trimethylcyclohexanone
4. High electrophilicity in 2,2,6-trimethylcyclohexanone