Starting from (R)-3-methylhex-1-yne as the substrate at the center of your page, draw a reaction map showing the regiochemical and stereochemical outcome or outcomes for each of the following series of reagents. (Draw the products.) Name each of your products (skip A, B, and H), including stereochemical designations for any chirality centers that are generated. A. HgSO4, H2SO4, H20 B. 1. 9-BBN; 2. H202, NaOH C. D. HBr E. xs HBr F. HBr, ROOR G. xs HBr, ROOR H. 1.03; 2. H2O 1. H2, Lindlar's catalyst Br2, CC14
Starting from (R)-3-methylhex-1-yne as the substrate at the center of your page, draw a reaction map showing the regiochemical and stereochemical outcome or outcomes for each of the following series of reagents. (Draw the products.) Name each of your products (skip A, B, and H), including stereochemical designations for any chirality centers that are generated. A. HgSO4, H2SO4, H20 B. 1. 9-BBN; 2. H202, NaOH C. D. HBr E. xs HBr F. HBr, ROOR G. xs HBr, ROOR H. 1.03; 2. H2O 1. H2, Lindlar's catalyst Br2, CC14
Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter16: Aldehydes And Ketones
Section: Chapter Questions
Problem 16.67P: Treatment of -D-glucose with methanol in the presence of an acid catalyst converts it into a mixture...
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