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
There is only one –NH2 group involved in semicarbazone formation out of two –NH2 group. It is due to:
1. Resonance of one type of –NH2 group
2. Inductive effect of one type of –NH2 group
3. Hyperconjugation of one type of –NH2 group
4. Reverse hyperconjugation of one type of -NH2 group