EtOH,KOHAmajor

Product (A) is:

1.

2.

3.

4.

Subtopic:  Chemical Properties |
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Product A is:

1.     2.   
3.    4.
Subtopic:  Chemical Properties |
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(A)In the above reaction, maximum Saytzeff product will obtained when
     (a) X = I    (b) X = -Cl      (c) X = -Br       (d) X = -F

(B) In the above reaction Hofmann product is major when X is:
      (a) -I          (b) -Cl            (c) -Br             (d) -F

1. A- a , B - d

2. A- b, B - c

3. A -c , B - a 

4. A - d, B -d

Subtopic:  Chemical Properties |
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Major product of the above reaction is:

1. 

2. 

3. 

4. 

Subtopic:  Mechanism of Reactions | Chemical Properties |

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Major product is :-
 

1.         
2. 

3.           
4.

Subtopic:  Mechanism of Reactions | Chemical Properties |
 75%
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Addition of KI accelerates the hydrolysis of primary alkyl halides because:

1. KI is soluble in organic solvents

2. The iodide ion is a weak base and a poor leaving group

3. The iodide ion is a strong base

4. The iodide ion is a powerful nucleophile as well as a good leaving group

Subtopic:  Chemical Properties |
 78%

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Consider the nucleophilic attacks given below. Select in each pair that shows the greater SN2 reaction rate.

(A)  

(B)  

(C)  

(D)  


     A   B    C     D
1.  II   IV   VI   VIII
2.  II   III   V    VIII
3.  I    III   V    VIII
4.  I    III   V    VII 
 

Subtopic:  Mechanism of Reactions | Chemical Properties |
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What is the major product of the following reaction?

H2C=CH-CH2-OH excessHBr Product

1.  CH3-CH|Br-CH2-Br

2.  H2C=CH-CH2-Br

3.  CH3-CH|Br-CH2-OH

4.  CH3-CH|OH-CH2-OH

Subtopic:  Mechanism of Reactions | Chemical Properties |
 64%
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NBS(A)CH3SNa(B), Product (B) is:

1.

2.  

3. 

4. None of the above

Subtopic:  Mechanism of Reactions | Chemical Properties |
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Which of the following reactant will not favour nucleophilic substitution reaction ?

1. 

2. Ph-Br

3. CH3-C||CH3CH3-CH2-Br

4. All of the above

Subtopic:  Mechanism of Reactions | Chemical Properties |
 62%

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