Which of the following is the most unlikely resonance structure for the p-nitrophenoxide ion?

1. 2.
3. 4.

Subtopic:  Electron Displacement Effects |
 57%
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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 (inductive effect) is shown by:

1. -CH3

2. -OH

3. -F

4. -C6H5

Subtopic:  Electron Displacement Effects |
 85%
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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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Arrange H, CH₃, C₂H₅, and C₃H₇ in order of increasing positive inductive effect:

1. H < CH3 < C2H5 < C3H7

2. H> CH3 <C2H5 > C3H7

3. H < C2H5 < CH3 <C3H7

4. None of the above

Subtopic:  Electron Displacement Effects |
 82%
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To which ring size cycloalkanes, Baeyer’s strain theory is not valid?

(1) 3 carbon

(2) 4 carbon

(3) 5 carbon

(4) ≥6 carbon

Subtopic:  Hybridisation & Structure of Carbon Compounds |
 68%
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The shifting of electrons of  multiple bonds under the influence of a reagent is called:

1. I-effect

2. E-effect

3. M-effect

4. None of the above.

Subtopic:  Electron Displacement Effects |
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Which of the following statements accurately describes the stability of allyl and propyl carbocations?

1. Allyl carbocation (CH2=CH-CH2+) is more stable than propyl carbocation

2. Propyl carbocation is more stable than allyl carbocation

3. Both are equally stable

4. None of the above

Subtopic:  Reaction Intermediates ; Preparation & Properties |
 68%
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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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