Chem 334 - Fall 2001
Organic Chemistry I
Dr. Carl C. Wamser
1. (4 points) Give a complete name for the following, including designation of stereochemistry at each stereocenter.
a) 
(S)-2,4-dimethyl-1,2-pentanediol
b) 
(1S,3R)-3-bromo-1-methylcyclohexanol
2. (2 points) Identify the relationship between the following pairs of structures. Options are:
A - identical, B - enantiomers, C - conformers, D - diastereomers,
E - constitutional isomers,
F - non-isomeric, G - other
a) 
A - identical
b) 
B - enantiomers
3. (4 points) Write a complete mechanism for the following reaction. Show all steps and electron-pushing arrows, but just show the pathway to the indicated product. Carefully show the stereochemistry at each step. Include structures for all stereoisomers of the indicated product that would be expected from this reaction.
