Alkynes, Part 3. 
Alkynes, Part 3.
by UC Irvine / David Van Vranken
Video Lecture 11 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 11. Organic Chemistry -- Alkynes -- Part 3












Recorded on February 4, 2013.

Index of Topics:
00:29- A Perfect Red
02:42- Cochineal
05:07- 11.7: Best Alkynes for H-X Addition
11:49- 11.7: Worst Alkynes for H-X Addition
15:58- 11.8: Addition of Cl2 and Br2 to Alkynes
21:52- 11.8: Addition of Cl2 and Br2 to Alkynes-Add two equivalents of halogen to generate the tetrahalide
24:58- 11.9: Hydration: Addition of H2O
28:33- 11.9: Initial Product=enol
31:58- 11.9: Mechanism
37:38- 11.9: Keto-Enol Tautomerism

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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