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Unformatted text preview: Cl (25C) Br (150C) Primary C-H 1 1 1 Secondary C-H 1.2 3.9 82 Tertiary C-H 1.4 5.1 1600 X 2 hv X 2 hv 3. Provide the complete, stepwise mechanism for the following transformations. Br 2 h Br Br HBr peroxide h 4. Devise a synthesis of each target molecule from the given starting material in the following retrosyntheses shown below. Provide the reagents and conditions for each step in the synthesis. OH Br Br O...
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This note was uploaded on 09/26/2011 for the course CHEM 3053 taught by Professor Any during the Fall '08 term at The University of Oklahoma.
- Fall '08