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Lecture 22. Conjugation, Resonance, Diels-Alder Reactions, Part 2

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Lecture 22. Conjugation, Resonance, Diels-Alder Reactions, Part 2
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22
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26
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CC Attribution 3.0 Unported:
You are free to use, adapt and copy, distribute and transmit the work or content in adapted or unchanged form for any legal purpose as long as the work is attributed to the author in the manner specified by the author or licensor.
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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. This video is part of a 26-lecture undergraduate-level course titled "Organic Chemistry" taught at UC Irvine by Professor David Van Vranken. 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