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Interactive video lesson plan for: 25. C-13 and 2D NMR. Electrophilic Aromatic Substitution

Activity overview:

Freshman Organic Chemistry II (CHEM 125B)

Proton decoupling simplifies C-13 NMR spectra. Dilute double labeling with C-13 confirmed the complex rearrangement scheme in steroid biosynthesis. Two-dimensional NMR yields correlations between NMR signals that underlie structural determination of proteins and identification of the mechanism of a rapid carbocation rearrangement. Substitution of an electrophile for a proton on an aromatic ring proceeds by a two-step association-dissociation mechanism involving a cyclohexadienyl cation intermediate. The relative rates of forming various products from substituted benzenes correlates with the substituents' influences on the stability of the various cyclohexadienyl cation intermediates. The spectrum of electrophile reactivities is very broad. Important contributions for activating electrophiles were made by Friedel and Crafts working in Paris.

00:00 - Chapter 1. Proton Decoupling
04:39 - Chapter 2. C-13 NMR: Double Labeling and Lanosterol Biosynthesis
19:51 - Chapter 3. 2-D NMR for Protein Structure and Rearrangement Rate
39:07 - Chapter 4. Electrophilic Aromatic Substitution: Substituent Effects
46:25 - Chapter 5. Electrophile Activation: Friedel and Crafts

Complete course materials are available at the Open Yale Courses website: http://oyc.yale.edu

This course was recorded in Spring 2011.

Tagged under: decoupling,C-13 NMR,double labeling,lanosterol,biosynthesis,correlation,2-D NMR,NOE,methide shift,activating,deactivating,ortho/para directing,meta directing,AlCl3,nitro group,nitration,Friedel-Crafts

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