CH3CHO and C6H5CH2CHO can be distinguished by:

1. Benedict test

2. Iodoform test

3. Tollen's reagent test

4. Fehling solution test

Subtopic:  Isomers & Reaction Mechanism |
 66%
From NCERT
AIPMT - 2012
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Which acid doesn't exhibit optical isomerism?

1. Maleic acid

2. α-amino acid

3. Lactic acid

4. Tartaric acid

Subtopic:  Isomers & Reaction Mechanism |
 54%
From NCERT
AIPMT - 2012
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The Clemmensen reduction of a ketone is carried out in the presence of:

1. Zn-Hg with HCl

2. LiAlH4

3. H2 and Pt as a catalyst

4. Glycol with KOH

Subtopic:  Name Reaction |
 93%
From NCERT
AIPMT - 2011
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The product 'D' in the below-mentioned reaction will be:

 

1.  2.
3. 4.
 

Subtopic:  Isomers & Reaction Mechanism |
 65%
From NCERT
AIPMT - 2011
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The example of a nucleophilic substitution reaction among the following is:

1.
2.
3.
4.
Subtopic:  Isomers & Reaction Mechanism |
 65%
From NCERT
AIPMT - 2011
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The compound that is most susceptible to a nucleophilic attack in the carbonyl group is:

1. CH3COOCH3

2. CH3CONH2

3. CH3COOCOCH3

4. CH3COCl

Subtopic:  Isomers & Reaction Mechanism |
 67%
AIPMT - 2010
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In a basic medium, acetophenone yields a stable compound A with C2H5ONa.

The structure of A is:

1.  2.
3. 4.
Subtopic:  Name Reaction |
 65%
From NCERT
AIPMT - 2008
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A strong base can abstract an α-hydrogen from:

1. Alkene
2. Amine
3. Ketone
4. Alkane
Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 70%
From NCERT
AIPMT - 2008
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A compound with the molecular formula C5H10 that yields acetone on ozonolysis is:
1. 2-Methyl-2-butene
2. 2-Methyl-1-butene
3. Cyclopentane
4. 3-Methyl-1-butene

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 81%
From NCERT
AIPMT - 2007
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The compound on hydrolysis of 50% aqueous sodium hydroxide that produces the corresponding alcohol and acid is:

1. C6H5CH2CHO

2. C6H5CHO

3. CH3CH2CH2CHO

4. CH3-C||O-CH3

Subtopic:  Name Reaction |
 72%
From NCERT
AIPMT - 2007
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