Notifications
Clear all
Addition of HI to double bond of propene yields isopropyl iodide and not n-propyl iodide as the major product, because addition proceeds through
0
14/02/2022 5:55 pm
Topic starter
Addition of HI to double bond of propene yields isopropyl iodide and not n-propyl iodide as the major product, because addition proceeds through
(a) a more stable carbonium ion
(b) a more stable carbanion
(c) a more stable free radical
(d) homolysis
Answer
Add a comment
Add a comment
Topic Tags
1 Answer
0
14/02/2022 5:58 pm
Correct answer: (a) a more stable carbonium ion
Explanation:
All are examples of electrophilic addition reactions and involve the formation of stable carbocation leading to the formation of addition product according to Markovnikov’s rule.
Add a comment
Add a comment
Forum Jump:
Related Topics
-
Product (A) of above reaction is:
3 years ago
-
Which of the following is an aromatic species?
3 years ago
-
Arrange the following in decreasing order of reactivity towards EAS (electrophilic aromatic substitution)
3 years ago
-
Identify the position where electrophilic aromatic substitution (EAS) is most favourable.
3 years ago
-
The two compounds A and B obtained from 1-butyne can be distinguished by
3 years ago
Forum Information
- 321 Forums
- 27.3 K Topics
- 53.8 K Posts
- 0 Online
- 12.4 K Members
Our newest member: Stripchat
Forum Icons:
Forum contains no unread posts
Forum contains unread posts
Topic Icons:
Not Replied
Replied
Active
Hot
Sticky
Unapproved
Solved
Private
Closed