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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 |
Level 3: 35%-60%
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Which of the following is not nucleophile:-

1. 

2. 

3. 

4. 

Subtopic:  Nucleophile & Electrophile |
 83%
Level 1: 80%+
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Correct order of acidic strength for following is:-

1. I > II > III > IV

2. I > III > II > IV

3. IV > III > I > II

4. III > I > II > IV

Subtopic:  Acidic & Basic Character |
 61%
Level 2: 60%+
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Which of the following although have α-hydrogen but does not show tautomerism :-

1.

2. 

3. 

4. 

Subtopic:  Structural Isomers |
 68%
Level 2: 60%+
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The molecule that exhibits non-planarity is:

1.  2. 
3.  4. 
Subtopic:  Aromaticity & Polarity |
 68%
Level 2: 60%+
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The aromatic compound among the following is:-

1. 2.
3. 4.
Subtopic:  Aromaticity & Polarity |
 77%
Level 2: 60%+
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Which carbocation is the most stable among the options provided?

1. 2.
3. 4.

Subtopic:  Reaction Intermediates ; Preparation & Properties |
 80%
Level 1: 80%+
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The geometrical isomerism is shown by:-

1.  

2.  

3.  

4.  

Subtopic:  Stereo Isomers |
 64%
Level 2: 60%+
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Correct stability order of the following carbocation:-

(1) ii > i > iii > iv

(2) i > ii > iii > iv

(3) iii > i > ii > iv

(4) iv > i > ii > iii

Subtopic:  Reaction Intermediates ; Preparation & Properties |
Level 3: 35%-60%
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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%
Level 2: 60%+
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