Conjugation, Resonance, Diels-Alder Reactions, Part 2. 
Conjugation, Resonance, Diels-Alder Reactions, Part 2.
by UC Irvine / David Van Vranken
Video Lecture 22 of 26
Copyright Information: Vranken, David Van. Organic Chemistry 51B (UCI OpenCourseWare: University of California, Irvine), [January 28, 2015]. License: Creative Commons Attribution-ShareAlike 3.0 United States License (
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Date Added: January 28, 2015

Lecture Description

Lec 22. Organic Chemistry -- Conjugation, Resonance, Diels-Alder Reactions -- Part 2

Recorded March 6, 2013.

Index of Topics:
00:13- A molecule today, a barrel tomorrow
00:42- Fracking
04:57- 16.12: The Diels-Alder Reaction
10:42- 16.13: Diene Requires an s-cis conformation
14:53- 16.13: Stereospecificity in the Diels-Alder Reaction
21:08- 16.13: Drawing Bridged Bicyclic Products of Diels-Alder Reactions
29:41- 16.13: The Endo Rule for Cyclic Dienes

CHAPTER 17-Benzene and Aromatic Compounds
34:05- 17.1: The C=C pi bonds in benzene exhibit low reactivity
39:19- 17.3: Disubstituted benzene rings: ortho, meta, and para relationships
45:06- 17.4: C NMR Spectroscopy
47:14- 17.4: H NMR Spectroscopy

Course Index

Course Description

This is the second quarter of the organic chemistry series. Topics covered include: Fundamental concepts relating to carbon compounds with emphasis on structural theory and the nature of chemical bonding, stereochemistry, reaction mechanisms, and spectroscopic, physical, and chemical properties of the principal classes of carbon compounds.


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