The order of basicity of

in water is

1.  IV < III < I < II

2.  II < I < IV < III

3.  IV < I < III < II

4.  II < III < I < IV

Subtopic:  Acidic & Basic Character |
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The order of basicity of the following compounds is:

     

1.  I > II > IV > III

2.  IV > II > I > III

3.  III > II > I > IV

4.  I > II > III > IV

Subtopic:  Acidic & Basic Character |
 57%
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The most basic nitrogen in the following compounds is

             

1.  I

2.  II

3.  III

4.  IV

Subtopic:  Acidic & Basic Character |

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Which of the following molecules cannot show geometric isomerism?

1.  CH3CH = NOH

2.  CH32C = NOH

3.  HO - C = N - OH

4.  

Subtopic:  Stereo Isomers |
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The order of acidity of compounds I - IV, is

1.  I < III < II < IV

2.  IV < I < II < III

3.  III < I < II < IV

4.  II < IV < III < I

Subtopic:  Acidic & Basic Character |
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The sequence of steps involved in aromatic nucleophilic substitution involving a benzyne intermediate is

1.  Addition-elimination

2.  Elimination-addition

3.  Addition-rearrangement

4.  Elimination-rearrangement

Subtopic:  Reaction Intermediates ; Preparation & Properties |

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Levonorgestrel is a commonly used contraceptive. The number of chiral centers present in this molecules are

 

1.  4

2.  5

3.  6

4.  7

Subtopic:  Stereo Isomers |
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The increasing reactivity of the sites (a-d) in the following compound in SN1 reaction is

       

1.  d > b > c > a

2.  d > c > a > b

3.  d > c > b > a

4.  c > d > b > a

Subtopic:  Electron Displacement Effects |
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Pairs of functional isomers  possible of molecular formula C4H10O are:

1. 2

2. 4

3. 8

4. 12

Subtopic:  Structural Isomers |
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Which type of structure(s) is/are possible for C3H6O?

1. Cyclic alcohols

2. Cyclic Ether

3. Ketone

4. All of the above

Subtopic:  Structural Isomers |
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