Electrophilic Aromatic Substitution. 
Electrophilic Aromatic Substitution.
by UC Irvine / David Van Vranken
Video Lecture 24 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 24. Organic Chemistry -- Electrophilic Aromatic Substitution -- Part 1












Recorded on March 11, 2013.

Index of Topics:
00:36- Natural Does Not Mean Safe
01:43- Molecular structure of allantoin

CHAPTER 18-Electrophilic Aromatic Substitution=E.A.S.
04:00- Chapter 18 Introduction
08:51- 18.1: Five Important Electrophilic Aromatic Substitution Reactions
14:39- 18.2: Two-Step Mechanism for E.A.S.
22:33- 18.3: Dalogenation with FeX3 and X2
31:05- 18.4: Nitration with HNO3 and H2S04
39:48- 18.4: Sulfation with SO3 and H2SO4
45:56- 18.5: Friedel-Crafts Acylation with RCOCl and AlCl3

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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