The hydrogenation of benzoyl chloride in the presence of Pd and BaSO4 gives:

1. Benzyl alcohol

2. Benzaldehyde

3. Benzoic acid

4. Phenol

Subtopic:  Name Reaction |
 91%
Level 1: 80%+
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Oxalic acid on reduction with zinc and H2SO4 gives:

1. Glycol

2. Glyoxal

3. Glyoxalic acid

4. Glycolic acid

Subtopic:  Carboxylic Acids: Preparation & Properties |
Level 4: Below 35%
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X + CH3COOH   →   Ester  +  H2O  
X is:

1. Alcohol 2. Pyridine
3. Secondary amine 4. Acid
Subtopic:  Carboxylic Acids: Preparation & Properties |
 88%
Level 1: 80%+
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Lactic acid on oxidation with alkaline potassium permanganate gives:

1. Propionic acid

2. Cinnamic acid

3. Pyruvic acid

4. Tartaric acid

Subtopic:  Carboxylic Acids: Preparation & Properties |
 58%
Level 3: 35%-60%
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The compound that can give a positive iodoform test is:

1. 2-Phenylethanol

2. Pentanal

3. 3-Pentanol

4. 1-Phenylethanol

Subtopic:  Name Reaction |
 58%
Level 3: 35%-60%
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Which reagent is used to convert benzoic acid into benzoyl chloride?

1. Cl2, hv

2. SO2

3. SOCl2

4. Cl2, H2O

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
 80%
Level 1: 80%+
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When treated with alkali and iodine, what substance will not give iodoform?
1. Acetone 2. Ethanol
3. Diethyl ketone 4. Isopropyl alcohol
Subtopic:  Name Reaction |
 77%
Level 2: 60%+
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The compound that responds to Tollen's test is

1. CH3COCH3

2. CH3CHO

3. CH3COOH

4. C2H5OC2H5

Subtopic:  Name Reaction |
 89%
Level 1: 80%+
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Concentrated sodium hydroxide and benzaldehyde react to produce:

1. Cinnamic acid

2. Hydrobenzamide

3. Benzyl alcohol

4. Benzophenone

Subtopic:  Name Reaction |
 78%
Level 2: 60%+
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An alkene “A” on reaction with O3 and Zn - H2O gives propanone and ethanal in an equimolar ratio. The addition of HCl to alkene “A” gives “B” as the major product. The structure of product “B” is:

1.  2.
3. 4.
 

Subtopic:  Isomers & Reaction Mechanism |
 84%
Level 1: 80%+
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