CHEM 263 - Final Exam - June 17, 2005

CHEM 263 - Final Exam - June 17, 2005 - Chemistry...

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Chemistry Department University of Alberta CHEM 263 Final Exam June 17, 2005 1. Name five (5) of the following structures: a. b. c. d.
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e. f. 2. Give the structural formula of five (5) of the following compounds: a. L-phenylalanine b. 3-methylbutanenitrile c. ( R )-2-pentanamine d. 2-ethoxy-3-phenylbutanal e. N -ethyl- N -methylpentanamide f. glycerol 3. Give the structure(s) of the principle organic products of ten (10) of the following reactions: a.
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b. c. d. e. f.
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g. h. i. j. k.
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l. 4. What reagent(s) would you use to effect ten (10) of the following conversions? a. b. c. d.
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e. f. g. h. i. j.
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k. l. 5. Provide synthetic pathways for the following transformations: a. b.
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c. 6. The IR and 1 H NMR spectra of a compound of molecular formula C 6 H 15 N are given below. Propose a structure for this compound: SDBSWeb: http://www.aist.go.jp/RIODB/SDBS/ (12-06-05)
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7. a. Circle the most stable of the following carbocations: (CH 3 ) 3 C + Cl 3 C + CH 2 =CHCH 2 + b. Circle the weakest of the following acids:
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This note was uploaded on 07/05/2008 for the course CHEM 263 taught by Professor Blackburn during the Summer '05 term at Manitoba.

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CHEM 263 - Final Exam - June 17, 2005 - Chemistry...

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