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Aldol condensation will not take place in

1. HCHO 

2. CH3CHO

3. CH3COCH3

4. CH3CH2CHO

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 87%
Level 1: 80%+
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In the below reaction, product 'P' is:

1.  2.
3. 4.
Subtopic:  Carboxylic Acids: Preparation & Properties |
 83%
Level 1: 80%+
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The -OH group of an alcohol or the -COOH group of a carboxylic acid can be replaced by -Cl using     

1. phosphorus pentachloride

2. hypochlorous acid

3. chlorine

4. hydrochloric acid

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 74%
Level 2: 60%+
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What ester produces a white crystalline acid when boiled with KOH, cooled, and acidified with conc. HCl?

1. Methyl acetate 

2. Ethyl acetate

3. Ethyl formate 

4. Ethyl benzoate

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
Level 3: 35%-60%
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The compound formed when malonic acid heated with urea, is                  

1. cinnamic acid

2. butyric acid

3. barbituric acid

4. crotonic acid

Subtopic:  Isomers & Reaction Mechanism |
Level 3: 35%-60%
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Trichloroacetaldehyde, CCl3CHO reacts with chlorobenzene in the presence of sulphuric acid and produces                                                                         
 

1.
2.
3.
4.

1.  

2.  

3.  

4.  

Subtopic:  Isomers & Reaction Mechanism |
 51%
Level 3: 35%-60%
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What compound results from the catalytic dehydrogenation of a primary alcohol?

1. Aldehyde 

2. Ketone 

3. Alkene

4. Acid 

Subtopic:  Isomers & Reaction Mechanism |
 73%
Level 2: 60%+
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The compound which on reduction with LiAlH4 gives two diffrent alcohols:

1. CH3COOCH3                         

2.  CH3COOC2H5

3. CH3COCH3                           

4.  CH3CHO

Subtopic:  Aldehydes & Ketones: Preparation & Properties | Isomers & Reaction Mechanism | Acid Derivatives - Preparation, Properties & Uses |
Level 3: 35%-60%
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HCHO and HCOOH are distinguished by treating with:

1. Tollens reagent

2. NaHCO3

3. Fehling's Solution

4. Benedict Solution

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 61%
Level 2: 60%+
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Lacrymator or tear gas is:

1. C6H5COCl                               

2. C6H5OC6H5

3. C6H5COCH2Cl                         

4. C6H5COCH3

Subtopic:  Acid Derivatives - Preparation, Properties & Uses | Name Reaction |
 52%
Level 3: 35%-60%
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