Fries Rearrangement
Interactive Video
•
Engineering, Chemistry, Science
•
11th Grade - University
•
Hard
Wayground Content
FREE Resource
The video explains the Fries rearrangement, a reaction named after Karl Fries, involving the rearrangement of aryl esters to form ortho and para products. It discusses the role of Lewis and Bronsted-Lowry acids, the reaction's reversibility, and the mechanism involving acylium ions. Crossover studies show intermolecular reactions, and the reaction's industrial applications are limited by harsh conditions. The anionic Fries rearrangement achieves ortho selectivity using strong bases, with applications in various substrates.
Read more
1 questions
Show all answers
1.
OPEN ENDED QUESTION
3 mins • 1 pt
What new insight or understanding did you gain from this video?
Evaluate responses using AI:
OFF
Access all questions and much more by creating a free account
Create resources
Host any resource
Get auto-graded reports
Continue with Google
Continue with Email
Continue with Classlink
Continue with Clever
or continue with
Microsoft
%20(1).png)
Apple
Others
Already have an account?
