Chem 51C. Lec 02. Organic Chemistry: Reactivity of Carbonyl Compounds, Reduction of Aldehydes and Ketones with Hydride Nucleophiles (English)


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UCI Chem 51C Organic Chemistry (Spring 2012)
Lec 02. Organic Chemistry -- Reactivity of Carbonyl Compounds, Reduction of Aldehydes and Ketones with Hydride Nucleophiles --
View the complete course: http://ocw.uci.edu/courses/chem_51c_organic_chemistry.html
Instructor: James S. Nowick, Ph.D.


License: Creative Commons BY-NC-SA
Terms of Use: http://ocw.uci.edu/info.
More courses at http://ocw.uci.edu


Description: This is the third quarter course in 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. Organic Chemistry 51C is part of OpenChem. http://ocw.uci.edu/collections/open_chemistry.html


Recorded on April 5, 2012


Index of Topics:
-1:00    Reactivity with Nucleophilic
-4:08    Resonance in a Carbonyl group
-8:41    Nucleophiles and Carbonyls
-18:09    LiAlH4 and NaBH4
-26:29    Example Reaction
-32:38    Reduction
-44:10    Hydride Reducing Agents
-48:57    Sodium Hydride
-54:02    Oxidation State
-1:00:14    Reactivity Toward Nucleophiles
-1:08:44    Making Racemic Mixtures
-1:12:38    Chiral Hydride Reagent
-1:16:05    Tert-Butyl Cyclohexanone Example


Required attribution: Nowick, James S. Organic Chemistry 51C  (UCI OpenCourseWare: University of California, Irvine), http://ocw.uci.edu/courses/chem_51c_organic_chemistry.html [Access date]. License: Creative Commons Attribution-ShareAlike 3.0 United States License .


Author:
James Nowick Ph.D.
Title:
Professor
Department:
Chemistry
Creative Commons License
Chem 51C (Spring 2012): Reactivity of Carbonyl Compounds, Reduction of Aldehydes and Ketones with Hydride Nucleophiles by James Nowick is licensed under a Creative Commons Attribution Unported 3.0 License
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