Organic Chemistry II |
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Professor Carl C. Wamser |
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Chem 335 - Winter Term |
Pre-Quiz 12 |
(must be done in D2L before Tues., Jan. 22, 7:30 am)
1. Addition of an electrophile to benzene gives a delocalized carbocation with how many resonance forms?
a) 1
b) 2
* c) 3
d) more than 3
2. Which substituent is an activating, ortho,para-director
a) Cl
* b) OCH3
c) H
d) CN
3. Which compound will react fastest in a Friedel-Crafts alkylation?
a) benzene
b) benzoic acid
c) nitrobenzene
* d) toluene
4. The compound below that will be most reactive in a nucleophilic aromatic substitution is
* a) p-fluoronitrobenzene
b) p-chloronitrobenzene
c) p-bromonitrobenzene
d) p-iodonitrobenzene
5. If benzene is treated first with CH3Cl + AlCl3, and then with HNO3 + H2SO4, the major product is expected to be
a) m-nitrotoluene
* b) p-nitrotoluene
c) m-nitrobenzoic acid
d) p-nitrobenzoic acid