Which of the following compound exhibit optical isomerism?

1. 

2. 

3. 

4. All of these

Subtopic:  Stereo Isomers |
 72%
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Arrange the following in order of their reactivity toward electrophilic substitution reaction:

I. II.
III. Iv.
 
1. I > II > III > IV 2. IV > III > II > I
3. II > I > IV > III 4. II > I > III > IV
Subtopic:  Nucleophile & Electrophile |
 62%
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Which of the following compound requires minimum energy for free rotation across double bond between ring :

1. 2.
3. 4.

Subtopic:  Aromaticity & Polarity |
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The molecule that exhibits non-planarity is:
 

1.  2. 
3.  4. 

Subtopic:  Aromaticity & Polarity |
 68%
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The aromatic compound among the following is:-

1. 2.
3. 4.
Subtopic:  Aromaticity & Polarity |
 77%
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Which carbocation is the most stable among the options provided?

1. 2.
3. 4.

Subtopic:  Reaction Intermediates ; Preparation & Properties |
 79%
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The presence of a halogen on the benzene ring in a nitration reaction leads to:

1. Direct nitro group to come at meta and deactivate the ring due to –I effect of halogen.
2. Direct nitro group to come at ortho and para position and deactivate the ring due to –I effect of halogen.
3. Direct nitro group to come at meta and activate the ring toward nitration reaction.
4. Nitration reaction does not take place due to deactivation caused by –I effect of halogen.
Subtopic:  Types of Reaction |
 72%
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The pair of structures that does not represent isomers is:

1. 2.
3. 4.

Subtopic:  Structural Isomers |
 67%
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Which among these can exhibit tautomerism?

1. a only

2. b only

3. c only

4. a and c

Subtopic:  Structural Isomers |
 56%
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Total number of stereoisomers of the compound:-

1. 10

2. 8

3. 6

4. 4

Subtopic:  Stereo Isomers |
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