Organic Chemistry II |
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Professor Carl C. Wamser |
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Chem 335 - Winter 2007 |
Chapter 17 Homework |
Carey, pages 772 - 781 :
Problems 17.22 - 50
1. Write complete names
for each of the following:
a)
b)
2. Write a complete mechanism for the acid-catalyzed formation of the cyclic
acetal between acetone and cis-1,2-cyclopentanediol.
Explain why an acetal is not formed with the trans isomer.
3. Develop a synthetic sequence for 3-ethyl-3-hexanol that uses as organic starting
materials only alcohols having four carbons
or fewer.
4. Explain how acetone in the presence of radioactively-labelled
water (H2O-18) slowly becomes radioactive
itself.