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Unformatted text preview: 2 CHCH 2 OH OH HOCH 2 CHCH 2 OH Br and b. CH 3 CH CHCH 2 Br CH 3 CHCH Br CH 2 and c. CH 3 NH 2 H H NH 2 CH 3 CH 3 H NH 2 H NH 2 CH 3 and 4. Draw the eclipsed conformations of the four stereoisomers of 2-bromo-3-chloropentan-3-ol, including the R or S identification of each chirality center. threo isomers erythro isomers enantiomers enantiomers diastereomers diastereomers 5. a. Predict the products for the following reaction: O O O H b. Classify the type of reaction and provide a mechanism for the transformation. c. Will the product be chiral or achiral? d. Will the product be optically active? Why or why not?...
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- Fall '10
- Organic chemistry, Tartaric acid, dias ter eomers, CH CH 2O