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Unformatted text preview: provided. b) Draw a perspective drawing on the template provided. CHO HO H CH 2 OH H OH H O OH c) Given that D-threose has an optical rotation ( α ) = +34.4 o , what is the optical rotation ( α ) of L-threose? 4. (14 points) Monobromination of 2-methylpropane could produce 2 different constitutional isomers. Br 2 h υ , heat MAJOR product MINOR product a) Draw these 2 isomers (C 4 H 9 Br) in the boxes provided making sure to put each product in the appropriate box. b) Write out either one of the two propagation steps leading to the major product. Be sure to include the curved arrows that show the electron flow from reactants to products....
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This note was uploaded on 12/09/2011 for the course ENME 110 taught by Professor Irvine during the Spring '09 term at UMBC.
- Spring '09