Organic Chemistry II |
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Professor Carl C. Wamser |
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Chem 335 - Winter Term |
Pre-Quiz 13 |
(must be done in D2L before Tues., Jan. 29, 7:30 am)
1. Which isomer will show only a single peak in its proton NMR spectrum?
a) 1,1-dibromopropane
b) 1,2-dibromopropane
c) 1,3-dibromopropane
* d) 2,2-dibromopropane
2. In order to distinguish cyclononane from cyclodecane, which spectroscopy technique would be most useful?
a) proton NMR
b) infrared
* c) mass spectrometry
d) ultraviolet-visible
3. How many different signals (unique Hs) would you expect in the proton NMR spectrum of 2-chloropentane?
a) 2
b) 3
c) 4
* d) 5
4. A strong infrared absorption at 1710 cm-1 is most likely an indication of what functional group
* a) C=O
b) O-H
c) C=C
d) C-Br
5. The compound below expected to have an absoption at the longest wavelength in its ultraviolet-visible spectrum is
a) 1,3-cyclohexadiene
b) benzene
c) 1,3,5-hexatriene
* d) 1,3,5,7-octatetraene