Glucose and fructose are-

1. Chain isomers 2. Position isomers
3. Functional isomers 4. Optical isomers

Subtopic:  Stereo Isomers |
 63%
Level 2: 60%+
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The optically active compound among the following is-

1. Isobutyric acid

2. beta-Chloropropionic acid

3. Propionic acid

4. alpha-Chloropropionic acid

Subtopic:  Stereo Isomers |
 57%
Level 3: 35%-60%
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Which is incorrect about enantiomorphs?

(1) They rotate the plane of polarized light in different directions

(2) They have mostly identical physical properties

(3) They have same configuration

(4) They have different biological properties

Subtopic:  Stereo Isomers |
 55%
Level 3: 35%-60%
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The isomeric cis-2-Butene and trans-2-Butene can be distinguished on the basis of:

1. Their colour.

2. Their reduction products.

3. The products they give on ozonolysis..

4. The products they give on addition to bromine.

Subtopic:  Stereo Isomers |
 58%
Level 3: 35%-60%
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Number of optically active forms possible for a compound with the following formula are:

CHOCHOHCHOHCHOHCH2OH

1. 2 2. 4
3. 3 4. 8
Subtopic:  Conformational Isomers |
 56%
Level 3: 35%-60%
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The intermediate during the addition of HCl to propene in the presence of peroxide is:

1. CH3CHCH2Cl

2. CH3C+HCH3

3. CH3CH2CH2

4. CH3CH2C+H2

Subtopic:  Reaction Intermediates ; Preparation & Properties |
 53%
Level 3: 35%-60%
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The number of isomers for the compound with molecular formula C2BrCIFI is:

(1) 3

(2) 4

(3) 5

(4) 6

Subtopic:  Stereo Isomers |
Level 3: 35%-60%
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Geometrical isomerism is not shown by:

1. 

2. 

3. CH2=CClCH3

4. CH3-CH=CH-CH=CH2

Subtopic:  Stereo Isomers |
 73%
Level 2: 60%+
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The maximum number of stereoisomers possible for 3-hydroxy-2-methyl butanoic acid is:

1. 1               2. 2

3. 3               4. 4

Subtopic:  Stereo Isomers |
 69%
Level 2: 60%+
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The enol form of acetone after treatment with D2O gives:

1. OD
|
CH3C=CH2

2. O
||
CH3CCD3

3. OH
|
CH2=CCH2D

4. OD
|
CD2=CCD3

Subtopic:  Structural Isomers |
 59%
Level 3: 35%-60%
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