The relative stability order of carbanions CH≡C-, CH- and CH2=CH- is ____________

1. CHC->CH2=CH->CH3-

2. CH3->CH2=CH->CHC-

3. CHC-<CH2=CH->CH3-

4. CH2=CH-<CHC-<CH3-

Subtopic:  Reaction Intermediates ; Preparation & Properties |
 69%
Level 2: 60%+
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Which of the following is the strongest nucleophile in aprotic solvent?

1. Br-         
2. OH-
3. CN-        
4. CH3O-

Subtopic:  Nucleophile & Electrophile |
Level 4: Below 35%
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Which of the following is the most stable carbocation
 

1.
2.
3.
4.


 

Subtopic:  Reaction Intermediates ; Preparation & Properties |
 53%
Level 3: 35%-60%
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What is the decreasing order of acidity for the compounds given below?

1. III>IV>I>II 2. I>IV>III>II
3. II>I>III>IV 4. IV>III>I>II
Subtopic:  Acidic & Basic Character |
 78%
Level 2: 60%+
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The correct increasing order of carbon-carbon bond length in the given compounds is: 

1. III<II<I<IV

2. IV<I<II<III

3. I<II<III<IV

4. I<IV<III<II

Subtopic:  Hybridisation & Structure of Carbon Compounds |
 83%
Level 1: 80%+
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The IUPAC name of the following compounds is:
 

1. 1-Bromocyclohexane carboxylic acid

2. 3-Bromocyclohexanoic acid

3. 3-Bromoheptanoic acid

4. 3-Bromocyclohexanecarboxylic acid

Subtopic:  Nomenclature |
 52%
Level 3: 35%-60%
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The correct order of basicities of the following compounds is:

(1)

(2) CH3-CH2-NH2

(3) (CH3)2NH

(4) CH3-C||O-NH2

1. 2>1>3>4         

2. 1>3>2>4

3. 3>1>2>4         

4. 1>2>3>4

Subtopic:  Acidic & Basic Character |
 57%
Level 3: 35%-60%
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The most reactive of these compounds towards sulphonation is

1. Toluene                2. Chlorobenzene

3. Nitrobenzene        4. m-Xylene

Subtopic:  Nucleophile & Electrophile |
Level 3: 35%-60%
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How many geometrical isomers are possible of the following?

 CH3-CH=CH-CH=CH-CH3

1. 2             2. 3

3. 4             4. 6

Subtopic:  Stereo Isomers |
Level 3: 35%-60%
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The configuration of given tartaric acid is

 

1. 2R, 3R         2. 2R, 3S

3. 2S, 3S         4. 2S, 3R

Subtopic:  Stereo Isomers |
 64%
Level 2: 60%+
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