Organic Chemistry CHM 252 and CHM 254L
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CHM 252 Organic Chemistry II
Spring 2001
Workshop #7

  1. Use the structure of the Diels-Alder adduct to deduce the structure of product X in the reaction sequence below. Give a mechanism for the formation of X.



  2. Propose a mechanism for the following reaction.



  3. You are to synthesize THREE of the following target compounds shown below starting from benzene, acetylene, methanol, ethanol, potassium t-butoxide, maleic anhydride, acetic anhydride, ethylene oxide, acetyl chloride, and cyclohexene as your only sources of carbon.  For those that you do not finish, practice them on your own and try to come up with answers.

     

 

Spring WS #1 Spring WS #2 Spring WS #3 Spring WS #4 Spring WS#5 Spring WS #6 Spring WS #7 Spring WS #8 Spring WS #9 Spring WS #10 Spring WS #11 Spring WS #12 Leaders

Timm A. Knoerzer
email
Naz Chem. Dept.
Naz. Home Page

Last Updated Tuesday, March 13, 2001 12:31:28 PM