Given the following reaction:
CH3
CHO+HCNX
(Assume compound X has a chiral centre)
The optical activity associated with product X would be: 

1. Laevorotatory 
2. Dextrorotatory
3. Mesocompound
4. Racemic mixture

Subtopic:  Isomers & Reaction Mechanism |
 75%
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Benzophenone can be converted into benzene using 

1. anhydrous AlCl3

2. acidified dichromate

3. sodium amalgam in water

4. fused alkali

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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Which of the following react with NaOH to produce an acid and alcohol?

1. CH3COOH

2. HCHO

3. C6H5COOH

4. CH3CH2COOH

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 73%
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Which of the following is incorrect?

1. Fehling solution is used in detection of glucose

2. NaHSO3 is used in detection of carbonyl compounds

3. FeCl3 is used in detection of phenols

4. Tollen's reagent is used in detection of unsaturation.

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 74%
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Formaldehyde on condensation in presence of Ca(OH)2 gives

1. formose

2. fructose

3. maltose

4. xylose

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 55%
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In the following reaction, product 'P' is 

R-CO-Cl Pd-BaSO4H2 P

1. RCOOH

2. RCHO

3. RCH3

4. RCH2OH

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 89%
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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%
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CH3CHCl2, on hydrolysis will give

1. CH3CHO

2. CH3COOH

3. CHCl3

4. CH3CH2OH

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 72%
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The reagent used for the separation of acetaldehyde from acetophenone is 

1. NH2OH

2. NaHSO3

3.  NaOH/I2

4. C6H5NHNH2

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 60%
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Acetaldehyde gives orange coloured precipitate on treatment with

1. 2, 4-DNP

2. NH2OH

3. NaHSO3

4. NaOH

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 82%
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