(1) 
(2)
(3)
(4)None of these

Subtopic:  Reaction Intermediates |
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(CH3)3CCI + (CH3)3CO- K+ → Product

1. SN Product will be more

2. E2 Product will be more

3. Both will be the same

4. None of the above

Subtopic:  Hofmann's Elimination & Saytzeff Elimination |
 57%
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Neopentyl iodide is treated with aq. AgNO3 solution, a yellow precipitate is formed along with another compound which is

1. (CH3)3CCH2ONO2

2. 

3. (CH3)3CCH2OH

4. 

Subtopic:  Reaction Intermediates |
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The major end product of the following reaction is

1. 
2.
3.
4.

Z

Subtopic:  Reaction Intermediates |
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The product of following reacting is

(1) 
(2)
(3)
(4)
Subtopic:  Hofmann's Elimination & Saytzeff Elimination |
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The product in the given reaction is

(1) 
(2)
(3)
(4)
Subtopic:  SN1 & SN2 Reactions |
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Conversion of cyclohexene to cyclohexanol can be conveniently achieved by:

1. NaOH + H2O

2. Br2-H2O

3. Hydroboration, oxidation

4. Hydroboration hydrolysis

Subtopic:  SN1 & SN2 Reactions |
 60%
From NCERT
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Bromination of (E)-2-butenedioic acid gives

(1) (2R, 3S)-2, 3-dibromosuccinic acid

(2) (2R, 3R)-2, 3-dibroniosuccinic acid

(3) a mixture of (2R, 3R) and (2S, 3S)-2, 3-dibromosuccinic acid

(4) (2S, 3S)-2, 3-dibromosuccinic acid

Subtopic:  Hofmann's Elimination & Saytzeff Elimination |
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HBr(X) acetoneNaI(Y) (Major); Product (Y) is:

(1) cis-2-butene                                 

(2) trans-2-butene

(3) 1-butene                                   

(4) Iso-butene

 

Subtopic:  Reagents |
 65%
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Which position will be attacked most rapidly by the nitronium ion (-NO2)+ when the compound undergoes nitration with HNO3/H2SO4 :-

1. A

2. B

3. C

4. D

Subtopic:  Directive Effect of functional grp |
 59%
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