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- Column I Reactions Column II Mechanism a <img class=img-fluid question-image alt=image src=https://cdn.tardigrade.in/img/question/chemistry/804f39415b0c404ec2d7dd5f14f89b40-.png /> p Ring expansion b <img class=img-fluid question-image alt=image src=https://cdn.tardigrade.in/img/question/chemistry/38936b63956ad23e9bae3bc9dd9255bf-.png /> q Ring contraction c <img class=img-fluid question-image alt=image src=https://cdn.tardigrade.in/img/question/chemistry/5fd1c26518e840dcced276d524ae3477-.png /> r Carbocation d <img class=img-fluid question-image alt=image src=https://cdn.tardigrade.in/img/question/chemistry/1a05af4d4b670f0723dd8fe25d413ed3-.png /> s Rearrangement t Radical anion
Q.
Column I Reactions
Column II Mechanism
a

p
Ring expansion
b

q
Ring contraction
c

r
Carbocation
d

s
Rearrangement
t
Radical anion
Column I Reactions | Column II Mechanism | ||
---|---|---|---|
a | ![]() |
p | Ring expansion |
b | ![]() |
q | Ring contraction |
c | ![]() |
r | Carbocation |
d | ![]() |
s | Rearrangement |
t | Radical anion |
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Solution:
$( a \rightarrow q , r , s ; b \rightarrow p , r , s ; c \rightarrow s ; d \rightarrow r , s , t )$
c. It is an examnle of Beckmann rearrangement reaction.
d. It is an example of bimolecular reduction (formation of pinacol) followed by acid-catalysed rearrangement reaction to form pinacolone. The formation of pinacol proceeds by the formation of a radical anion intermediate.
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