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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/f2f3cc9feae0595e55f57279acf694be-.png /> p Vinylic radical b <img class=img-fluid question-image alt=image src=https://cdn.tardigrade.in/img/question/chemistry/555ea5daeb19e4702723a5b3da2ef0f6-.png /> q Radical anion c <img class=img-fluid question-image alt=image src=https://cdn.tardigrade.in/img/question/chemistry/8bac5f75802d1c9af174632e382c44ba-.png /> r trans-Vinylic anion d <img class=img-fluid question-image alt=image src=https://cdn.tardigrade.in/img/question/chemistry/80f4398e2ea0ea59c7c0363b83a539ff-.png /> s Concerted mechanism
Q.
Column I Reactions
Column II Mechanism
a
p
Vinylic radical
b
q
Radical anion
c
r
trans-Vinylic anion
d
s
Concerted mechanism
Column I Reactions | Column II Mechanism | ||
---|---|---|---|
a | p | Vinylic radical | |
b | q | Radical anion | |
c | r | trans-Vinylic anion | |
d | s | Concerted mechanism |
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Solution:
$( a \rightarrow q ; b \rightarrow p , q , r ; c \rightarrow s ; d \rightarrow s )$
a. It is pinacol formation which proceeds by radical anion.
b. It is Birch reduction which proceeds by the formation
c. It is an example of Claisen rearrangement reaction and proceeds by concerted mechanism.
d. It is an example of Diels-Alder reaction and proceeds by concerted mechanism.
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