DOC PREVIEW
UGA CHEM 2211 - Diels-Alder Reactions
Type Lecture Note
Pages 2

This preview shows page 1 out of 2 pages.

Save
View full document
Premium Document
Do you want full access? Go Premium and unlock all 2 pages.
Access to all documents
Download any document
Ad free experience

Unformatted text preview:

CHEM 2211 1st Edition Lecture 26 Outline of Last Lecture I II III IV V Delocalization Energy Criteria for Aromatic compounds Aromaticity of Heterocyclic compounds Antiaromaticity Drawing molecular orbitals and Frost Diagrams Outline of Current Lecture I Diels Alder Reactions Current Lecture I Diels Alder Reactions A Always produces a six membered ring B Diene can attack a dienophile from either the top face or the bottom face C Electron rich regions do not react with each other D Electron poor regions react with electron rich regions E Example F Diels Alder reaction can occur with cyclic compounds G The face that the diene attacks determines the stereochemistry of the molecule The first product occurs when top face is attacked the second occurs when bottom face is attacked


View Full Document

UGA CHEM 2211 - Diels-Alder Reactions

Type: Lecture Note
Pages: 2
Documents in this Course
Load more
Download Diels-Alder Reactions
Our administrator received your request to download this document. We will send you the file to your email shortly.
Loading Unlocking...
Login

Join to view Diels-Alder Reactions and access 3M+ class-specific study document.

or
We will never post anything without your permission.
Don't have an account?
Sign Up

Join to view Diels-Alder Reactions and access 3M+ class-specific study document.

or

By creating an account you agree to our Privacy Policy and Terms Of Use

Already a member?