The below structure is an example of :

1. Cyanohydrin 2. Hemiacetal
3. Acetal 4. Cyanoalcohol

Subtopic:  Isomers & Reaction Mechanism |
 71%
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The IUPAC name for \(\mathrm{CH}_3 \mathrm{COCH}_2 \mathrm{COCH}_3\) is:
1. Pentane-2,4-dione
2. Pentane-1,4-dione
3. Pentane-2,2-dione
4. Pentane-3,4-dione
Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 89%
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The structure of Hex-2-en-4-ynoic acid is:

1.
2.
3.
4. None of these
Subtopic:  Carboxylic Acids: Preparation & Properties |
 89%
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The IUPAC name for PhCOPh is:
1. Diphenylmethanone
2. Benzophenone
3. Dibenzylmethanone
4. Dibenzylketone

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 54%
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The major product formed when cyclohexanecarbaldehyde reacts with PhMgBr and H3O+ is:

1.  2.
3. 4.  None of these
Subtopic:  Aldehydes & Ketones: Preparation & Properties | Isomers & Reaction Mechanism |
 85%
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What is the major product of the reaction between cyclohexanecarbaldehyde and Tollens' reagent?

1.  2.
3. 4. None of these
Subtopic:  Aldehydes & Ketones: Preparation & Properties | Name Reaction |
 78%
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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

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 74%
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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) 

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 74%
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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
Subtopic:  Name Reaction |
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Cyclohexanone forms cyanohydrin in a good yield, but 2,2,6-trimethylcyclohexanone does not. It is due to:

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

Subtopic:  Name Reaction |
 77%
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