Electrophilic Aromatic Substitution, Part 3. 
Electrophilic Aromatic Substitution, Part 3.
by UC Irvine / David Van Vranken
Video Lecture 26 of 26
Copyright Information: Vranken, David Van. Organic Chemistry 51B (UCI OpenCourseWare: University of California, Irvine), http://ocw.uci.edu/courses/chem_51b_organic_chemistry.html [January 28, 2015]. License: Creative Commons Attribution-ShareAlike 3.0 United States License (http://creativecommons.org/licenses/by-sa/3.0/us/deed.en_US).
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Date Added: January 28, 2015

Lecture Description

Lec 26. Organic Chemistry -- Electrophilic Aromatic Substitution -- Part 3












Recorded on March 15, 2013

Index of Topics:
00:10- Removing Toxic Chemicals with POPs
00:43- Molecular Structures of POPs
04:02- Summary of EAS Substituent Effects: Know This Summary
07:41- 18.9: Over-Activated Anilines and Phenols
11:56- 18.11: EAS on Disubstituted Benzene Rings
15:58- 18.11: EAS on Disubsituted Benzene Rings-no substitution between meta-substituents
18:26- 18.13: Benzylic Bromination
21:48- 18.13: Benzylic Bromination- chalk board
25:11- 18.14B: Reduction of Acyl Side Chains
30:40- 18.14B: Reduction of Acyl Side Chains, example 2
33:52- 18.14C: Reduction of NO2 to NH2
39:28- 18.15: Mulit-step Synthesis

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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