The end product (C) in the below-mentioned reaction is:
\(H_3C-Br\xrightarrow{\bf KCN }A\xrightarrow{ \bf H_3O^+~~}B\xrightarrow[\bf\text{Ether}]{~~LiAlH_4~~}C\)


1. Acetone
2. Methane
3. Acetaldehyde
4. Ethyl alcohol
Subtopic:  Mechanism of Reactions |
 60%
From NCERT
AIPMT - 2012
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Which of the following compounds undergoes nucleophilic substitution reaction most easily?

1. 2.
3. 4.
Subtopic:  Mechanism of Reactions |
 78%
From NCERT
AIPMT - 2011
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Consider the reactions:

(i) \(\small{{(CH_3)}_2CHCH_2Br\ \xrightarrow[]{C_2H_5OH}{(CH_3)}_2CHCH_2OC_2H_5 + HBr}\)    
(ii) \(\small{{(CH_3)}_2CHCH_2Br\ \xrightarrow[]{C_2H_5O^-}{(CH_3)}_2CHCH_2OC_2H_5 + Br^-}\)    

The mechanisms of reactions (i) and (ii) are, respectively:
1. SN2 and SN1
2. SN1 and SN2
3. SN1 and SN1
4. SN2 and SN2
Subtopic:  Mechanism of Reactions |
 52%
From NCERT
AIPMT - 2011
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Which of the following reactions cannot form new carbon-carbon bonds?

1. Reimer-Tiemann reaction

2. Cannizaro reaction

3. Wurtz reaction

4. Friedel-Crafts acylation

Subtopic:  Mechanism of Reactions |
 62%
From NCERT
AIPMT - 2010
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For the following: 
(i) I- 
(ii) Cl- 
(iii) Br- 
The increasing order of nucleophilicity would be:

1. I-<Br-<Cl-

2. Cl-<Br-<I- 

3. I- <Cl-<Br-

4. Br-<Cl-<I-

Subtopic:  Mechanism of Reactions |
 63%
AIPMT - 2007
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