In which of the following SN1 reaction is feasible?

1.  
2.  
3.
4. 
Subtopic:  Mechanism of Reactions | Chemical Properties |
 82%
Level 1: 80%+
Please attempt this question first.
Hints
Please attempt this question first.

Assertion (A): Isopropyl chloride is more reactive than CH3Br in SN2 reactions. 
Reason (R): SN2 reactions are always accompanied by inversion of configuration. 
 
1.  Both (A) and (R) are True and (R) is the correct explanation of (A).
2. Both (A) and (R) are True but (R) is not the correct explanation of (A).
3. (A) is True but (R) is False.
4. (A) is False but (R) is True.
Subtopic:  Mechanism of Reactions | Chemical Properties |
 81%
Level 1: 80%+
Please attempt this question first.
Hints
Please attempt this question first.

The given reaction will be the fastest in which of the following solvents?
CH3 CH2 CH2 Br + NaCN - CH3 CH2 CH2 CN + NaBr 

1.  Ethanol

2.  Methanol

3.  N, N'-dimethylformamide (DMF)

4.  Water

Subtopic:  Mechanism of Reactions | Chemical Properties |
 81%
Level 1: 80%+
NEET - 2016
Hints

advertisementadvertisement

Match the column:
Column-I
(Name reaction)
Column -I
(Representation of reaction)
(P) Finkelstein reaction (I)
(Q) Lucas reaction (II)
(R) Wurtz reaction (III)
(S) Gattermann-Koch reaction (IV)

1. P-IV, Q-III, R-II, S-I
2. P-I, Q-II, R-III, S-IV
3. P-II, Q-III, R-I, S-IV
4. P-III, Q-II, R-I, S-IV
Subtopic:  Mechanism of Reactions |
 95%
Level 1: 80%+
Please attempt this question first.
Hints
Please attempt this question first.

The most reactive compound for SN2 reaction among the following is: 

1. 2.
3. 4.
Subtopic:  Mechanism of Reactions |
 90%
Level 1: 80%+
Please attempt this question first.
Hints
Please attempt this question first.

In the following pairs of halogen compounds, which compound undergoes faster SN1 reaction? 



The correct option is:

1.
2.
3.
4.
Subtopic:  Mechanism of Reactions |
 89%
Level 1: 80%+
Hints

advertisementadvertisement

Choose the incorrect statement regarding SN2 reactions:
1. As the concentration of nucleophiles increases, the reaction rate increases.
2. Both the attack of the nucleophile and the departure of the leaving group occur simultaneously.
3. Inversion of configuration occurs on asymmetric centers because the nucleophile attacks from the backside of the leaving group.
4. The SN2 mechanism is predominant in tertiary alkyl halides.
Subtopic:  Mechanism of Reactions |
 87%
Level 1: 80%+
Please attempt this question first.
Hints
Please attempt this question first.

 Product of reaction is :
 

1. 2.
3. 4.
Subtopic:  Mechanism of Reactions |
 87%
Level 1: 80%+
Hints

 Identify the compound Y in the following reaction.

1. 

2. 

3. 

4. 

 

Subtopic:  Mechanism of Reactions |
 87%
Level 1: 80%+
Please attempt this question first.
Hints

advertisementadvertisement

The major product C in the below-mentioned reaction is:
 
1. Propan-1-ol 2. Propan-2-ol
3. Propane 4. Propyne
Subtopic:  Mechanism of Reactions |
 82%
Level 1: 80%+
NEET - 2024
Hints