Organic Chemistry III |
||
Professor Carl C. Wamser |
||
Chem 336 - Spring 2006 |
Pre-Quiz 23/24 |
(must be done in WebCT before Mon., May 1, 8:30 am)
1. In the list below, the compound least reactive in an SN2 mechanism will be
a. allyl bromide
b. ethyl chloride
* c. bromobenzene
d. benzyl bromide
e. benzyl chloride
2. In the list below, the most reactive compound in nucleophilic substitution is
a. 1-fluoro-2,3-dinitrobenzene
* b. 1-fluoro-2,4-dinitrobenzene
c. 1-fluoro-3,5-dinitrobenzene
d. 1-bromo-2,3-dinitrobenzene
e. 1-bromo-2,4-dinitrobenzene
f. 1-bromo-3,5-dinitrobenzene
3. The most acidic phenol in the list below is
a. phenol
b. o-nitrophenol
c. m-nitrophenol
d. p-nitrophenol
* e. 2,4-dinitrophenol
4. The benzyne mechanism starting from m-fluoroethylbenzene could give
a. o-ethylaniline
b. m-ethylaniline
c. p-ethylaniline
d. both ortho and para isomers
e. both meta and para isomers
* f. ortho, meta, and para isomers
5. Which of the following is NOT an example of a quinone?
a. Alizarin
b. Coenzyme Q-10
* c. Pyrocatechol
d. Ubiquinone
e. Vitamin K