Organic Chemistry II |
||
Professor Carl C. Wamser |
||
Chem 335 - Winter Term |
Pre-Quiz 12 |
(must be done in Blackboard before Fri., Jan. 15, 8:30 am)
1. Bromination of nitrobenzene will give mainly
a. o-bromonitrobenzene
* b. m-bromonitrobenzene
c. p-bromonitrobenzene
d. both o- and p-bromonitrobenzene
2. A Friedel-Crafts acylation reaction will produce
a. an alkylbenzene
b. an alkene
c. an alcohol
* d. a ketone
e. a carboxylic acid
3. Wolff-Kishner reduction is used to convert
a. a ketone to an alcohol
b. an alkene to an alkane
c. an alcohol to an alkane
d. an alkyne to an alkane
* e. a ketone to an alkane
4. The preferred position for electrophilic substitution on naphthalene is
* a. the 1-position
b. the 2-position
c. the bridgehead position
5. The reactivity order in electrophilic substitution is
a. benzene > pyridine > pyrrole
b. benzene > pyrrole > pyridine
c. pyrrole > pyridine > benzene
* d. pyrrole > benzene > pyridine
e. pyridine > pyrrole > benzene
f. pyridine > benzene > pyrrole