(CH3)4N+ is neither an electrophile, nor a nucleophile because it:

1. does not have electron pair for donation as well as cannot attract electron pair

2. neither has electron pair available for donation nor can accommodate electron since all shells of N are fully occupied.

3. can act as Lewis acid and base

4. none of the above

Subtopic:  Nucleophile & Electrophile |
 76%
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Which of the following is an electrophilic reagent?

1. RO-

2. BF3

3. NH3

4. ROH

Subtopic:  Nucleophile & Electrophile |
 77%
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The-I effect is shown by:

1. -COOH

2. -CH3

3. -CH3CH2

4. -CHR2

Subtopic:  Electron Displacement Effects |
 88%
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Which of the following is singlet carbene?

1. (CH3)3C+

2. C2H5-CH

3. CH3CH2CH2-

4. CH=CH-CH2+

Subtopic:  Reaction Intermediates ; Preparation & Properties |
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Sulphur trioxide act as:

1. An electrophile             

2. A nucleophile

3. A homolytic agent         

4. A base

Subtopic:  Nucleophile & Electrophile |
 59%
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Allyl isocyanide has:

1. 9 σ, and 4π-bonds.

2. 8 σ, and 5π-bonds

3. 9 σ, and 3π-bonds, 

4. 8 σ, and 3 π bonds

Subtopic:  Hybridisation & Structure of Carbon Compounds |
 66%
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Buta-1,3-diene and But-2-yne are:

1. Position isomers

2. Functional isomers

3. Chain isomers

4. Tautomers

Subtopic:  Structural Isomers |
 76%
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Diastereomers can be separated by:

1. Fractional distillation

2. simple distillation

3. electrophoresis

4. all of these

Subtopic:  Stereo Isomers |
 59%
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In the following carbocations, the most stabile carbocation:

(1)  RCH2C+H3         

(2) 

 

(3)                

 (4) 

Subtopic:  Reaction Intermediates ; Preparation & Properties |
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The number of optical isomers of pent-3-en-2-ol is:

1. 2             

2. 4

3. 8             

4. 16

Subtopic:  Structural Isomers |
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