51B. Lecture 22. Conjugation, Resonance, Diels-Alder Reactions, Part 2.
Recorded March 6, 2013.
Index of Topics:
00:13- A molecule today, a barrel tomorrow
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
Required attribution: Vranken, David Van. Organic Chemistry 51B (UCI OpenCourseWare: University of California, Irvine), ocw.uci.edu/courses/chem_51b_org....html. [Access date]. License: Creative Commons Attribution-ShareAlike 3.0 United States License (creativecommons.org/licenses/by-...n_US).
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