Most stable radical is

1. 2.
3. 4.

Subtopic:  Electron Displacement Effects | Reaction Intermediates ; Preparation & Properties |
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Consider the acidity of the following carboxylic acids

(i) PhCOOH

(ii) o-NO2C6H4COOH

(iii) p-NO2C6H4COOH

(iv)m-NO2C6H4COOH

1. i>ii>iii>iv

2. ii>iv>iii>i

3. ii>iv>i>iii

4. ii>iii>iv>i

Subtopic:  Acidic & Basic Character |
 65%
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The correct order of basicities of the following compounds is:

1. 2>1>3>4         2. 1>3>2>4

3. 3>1>2>4         4. 1>2>3>4

Subtopic:  Acidic & Basic Character |
 56%

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The decreasing order of stability of the carbocations among the following is:

1. I>II>III          2. II>III>I

3. III>I>II          4. II>I>III

Subtopic:  Electron Displacement Effects | Reaction Intermediates ; Preparation & Properties |
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The IUPAC name of the compound given below is:

 

1. 1-Bromocyclohexanecarboxylic acid

2. 3-Bromocyclohexanoic acid

3. 3-Bromoheptanoic acid

4. 3-Bromocyclohexane-1-carboxylic acid

Subtopic:  Nomenclature |
 56%
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In the following compounds,

The order of basicity is:

1. IV>I>III>II

2. III>I>IV>II

3. II>I>III>IV

4. I>III>II>IV

Subtopic:  Acidic & Basic Character |
 57%
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Which of the following is the most stable carbocation

1. 

2. 

3. CH2=CH-CH2

4. CH2=CH

Subtopic:  Reaction Intermediates ; Preparation & Properties |
 66%

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A solution of (+)-2 chloro-2-phenylethane in toluene racemizes slowly in the presence of small amount of SbCl5 due to formation of

1. Carbanion           

2. Carbene

3. Free radical          

4. Carbocation

Subtopic:  Reaction Intermediates ; Preparation & Properties |
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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:  Acidic & Basic Character |
 71%
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Maximum enol content is in 

1. 

2.

3.

 

4. 

Subtopic:  Structural Isomers |

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