In which of the following compounds, the C—Cl bond ionization shall give the most stable carbonium ion?

1. 2.
3. 4.
Subtopic:  Reaction Intermediates ; Preparation & Properties |
 57%
From NCERT
NEET - 2015
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Arrange the following in increasing order of stability:
(a) \(\left(\mathrm{CH}_3\right)_2 \stackrel{\oplus}{\mathrm{C}}-\mathrm{CH}_2-\mathrm{CH}_3 \)
(b) \(\left(\mathrm{CH}_3\right)_3 \stackrel{\oplus}{\mathrm{C}} \)
(c) \(\left(\mathrm{CH}_3\right)_2 \stackrel{\oplus}{\mathrm{C}}\mathrm{H} \)
(d) \( \text {CH}_3 \stackrel{\oplus}{\mathrm{C}}\mathrm{H}_2\)
(e) \( \stackrel{\oplus}{\mathrm{C}}\mathrm{H}_3 \)
 
1. e < d < c < a < b 2. d < e < c < a < b
3. a < e < d < c < b 4. e < d < c < b < a
Subtopic:  Reaction Intermediates ; Preparation & Properties |
 75%
From NCERT
NEET - 2013
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\(\mathrm{CH_3-CH_3, \ CH_3-CH_2-CH_3, \ }\)
\(\mathrm{\left(CH_3\right)_2 CH-CH_3, }\) and \(\mathrm{CH_3-CH_2-CH\left(CH_3\right)_2 }\)

The increasing order of stability of the free radicals formed from homolytic fission of the above three alkanes is:

1. \(\mathrm{ (CH_3)_2 \dot{C}-CH_2 CH_3<CH_3-\dot{C} H-CH_3 \\ <CH_3-\dot{C} H_2<(CH_3)_3 \dot{C} }\)
2. \( \mathrm{CH_3-\dot{C} H_2<CH_3-\dot{C} H-CH_3 \\ <\left(CH_3\right)_2 \dot{C}-CH_2 CH_3<\left(CH_3\right)_3 \dot{C}}\)
3. \(\mathrm{CH_3-\dot{C} H_2<CH_3-\dot{C} H-CH_3\\ <\left(CH_3\right)_3 \dot{C}<\left(CH_3\right)_2 \dot{C}-CH_2 CH_3 }\)
4. \(\mathrm{ \left(CH_3\right)_3 \dot{C}<\left(CH_3\right)_2 \dot{C}-CH_2-CH_3 \\ <CH_3-\dot{C} H-CH_3<CH_3-\dot{C} H_2 }\)
Subtopic:  Reaction Intermediates ; Preparation & Properties |
 79%
From NCERT
NEET - 2013
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The most reactive compound towards electrophilic reagent among the following is:

1. option 2. option
3. option 4. option
Subtopic:  Reaction Intermediates ; Preparation & Properties |
 53%
From NCERT
AIPMT - 2010
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NEET 2023 - Target Batch - Aryan Raj Singh

The stability of carbanions in the following:
 
is in the order of:

1.  (1) > (2) > (3) > (4)

2.  (2) > (3) > (4) > (1)

3.  (4) > (2) > (3) > (1)

4.  (1) > (3) > (2) > (4)

Subtopic:  Reaction Intermediates ; Preparation & Properties |
 62%
AIPMT - 2008
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