practice_final_from01

practice_final_from01 - CHM 2210/0767 Final Exam May 2,...

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CHM 2210/0767 NAME (Last, First)_______________________________ Final Exam SS#___________________________________________ May 2, 2001 1. (5 pts.) a) Circle the most stable carbocation. + vs. + b) Circle the most stable alkene. vs. c) Circle the compound which contains the most acidic proton. vs. d) Circle the compound that will react faster by an S N 1 mechanism. Cl Cl vs. e) Circle the compound that will react faster in an S N 2 reaction. OTS I 2. (4 pts.) Name the following compounds. OH a)
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b) 3. (6 pts.) Draw the three most stable resonance structures for the radical given below. CH 2 4. (3 pts.) Consider the following pairs of structures. Identify the relationship between them by describing them as enantiomers (E), diastereomers (D), constitutional isomers (CI), or the same compound (S). a. H CH 2 OH Cl CH 2 OH HI I CH 2 OH H CH 2 OH Cl H vs. b. CH 3 C Cl C Cl CH 3 vs. H Br H Br
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c. Cl CH 3 H CH 3 HC l H CH 3 Cl CH 3 l 5.(7 pts.) Convert the dash and wedge structure below into a Fischer projection and label each chiral carbon as (R) or (S).
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This note was uploaded on 04/12/2008 for the course CHM 2210 taught by Professor Reynolds during the Fall '01 term at University of Florida.

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practice_final_from01 - CHM 2210/0767 Final Exam May 2,...

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