Organic Chemistry III |
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Professor Carl C. Wamser |
(must be done in WebCT before Wed., March 31, 8:30 am)
1) The hydrate of acetone could also be correctly named
a. 1,1-dihydroxypropane
b. 1,2-dihydroxypropane
c. 1,1-propanediol
d. 1,2-propanediol
* e. 2,2-propanediol
2) The product of hexanal with an ethyl Grignard reagent would be (after acid workup)
a. a primary alcohol
* b. a secondary alcohol
c. a tertiary alcohol
d. a ketone
e. none of the above
3) Of the compounds below, the most reactive towards nucleophilic addition is
* a. formaldehyde
b. acetaldehyde
c. acetone
d. 3-pentanone
4) A Wittig reagent would be useful for the synthesis of
a. cyclohexanone
b. benzoic acid
* c. styrene
d. pentanal
5) An enamine is formed from an aldehyde or ketone plus
a. a primary amine
* b. a secondary amine
c. a tertiary amine
d. none of the above