CH 234 Study Guide - Quiz Guide: Reamer, Opiate, Specific Rotation
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Ch 231 test 3 chapters 7, 8, 9 (nov. 7, 2006: you have 105 minutes to complete the exam. 1. (10 pts) predict the products of the following reactions. Include any important stereochemical information in your answers. See mcmurry study guide and student solutions manual problem 7. 43. Combined avg. through test iii:_________: (15 pts) when 4-penten-1-ol is treated with aqueous bromine, a cyclic bromo ether is formed, rather than the expected bromohydrin. See mcmurry study guide and student solutions manual problem 7. 49: as stated in class both before and after the test, the electron pushing for the first mechanistic step is incorrect as depicted in the solutions manual. Remember that intramolecular processes are usually faster than intermolecular reactions, especially when a 5- or 6-membered ring may be formed. S configurations to each of the indicated chirality centers in the molecule: S: (12 pts) supply the missing reactant, reagent(s), or products in the schemes below.
