Dr. Glaser's "Chemistry is in the News"
To Accompany Bruice, Organic Chemistry, 3/e.
Chapter 12. Mass Spectroscopy, Infrared Spectroscopy, and
Ultraviolet/Visible Spectroscopy.
Editorial Comments
"You can never believe what you read in the papers!" - You have heard it many times, right? Well, it depends on where you read it. Papers like the The New York Times and The Washington Post usually are quite accurate. And that is even true when it comes to science; the Science pages in The New York Times are quite outstanding. Althought there are times when one wonders. I remember well reading for the first time about "cold fusion". I was living in Connecticut back then and I was reading this article in The New York Times about the promise of "Cold Fusion". It was April 1, 1988. When I realized what date it was, I was quite amused and mentioned to my (future) wife that she should not miss reading this wonderful April hoax piece in the Times. Well, little did I know that the Times was actually serious at that time and it took a few more years until the "Cold Fusion" idea was put on ice. (For a really entertaining hoax, do take a look at the Great Moon Hoax.)Questions
Question 1:
What is the range of reciprocal wavenumbers (1/cm) for a typical infrared
spectrum? Which sub-range is referred to as the fingerprint region?
Answer 1:
Typical range for entire spectrum 400 - 4000 1/cm.
Range for fingerprint region 400 - 1,400 1/cm.
Question 2:
What types of vibrations are distinguished? Order these types of
vibrations according to decreasing energy.
Answer 2:
Stretching vibrations > bending vibrations > twisting vibrations.
Question 3:
Which one of the following molecules cannot be detected by Infrared
spectroscopy? CO2, CO, or O2?
Answer 3:
Vibrations are IR-active only if the dipole moment of the molecule changes
during the vibration. The oxygen molecule is symmetric and its only
vibration, the strechting mode, does not lead to a change in the
electrical dipole moment of the molecule. The dipole moment always is
zero. In contrast, the CO molecule is highly polar and, what matters, the
dipole changes during the vibration. For carbon dioxide, there are some
vibrations that are IR active (asymm. stretching) and some that are not
(symm. stretching).
Question 4:
The article talks about the Cassini mission to Saturn carrying infrared
spectroscopy equipment. Indeed, infrared spectroscopy is widely used in
astronomy. Take a look at this spectacular false-color image of
The Galactic
Center Across the Infrared. This pictures uses blues and reds for the
"infrared" and the "near-infrared" ranges, respectively. Is the
near-infrared region below 400 1/cm or above 4000 1/cm?
Answer 4:
Near-IR is between the IR- and UV-regions. Higher energy than IR. Above
4000 1/cm.
Chemistry
Online Exploratory.
Take a look at the visualization center of Chapter 12
on infrared spectroscopy and note the links "Freqs". Follow these
links to find the results of theoretical calculations of the vibrational
properties. You will find computed vibrational frequencies as well as
computed intensities of these various vibrational modes. Read the
frequency files of carbon dioxide, carbon disulfide and of carbon
oxysulfide and find the vibrational frequencies of the symmetric anf
asymmetric stretching vibrations. Compare & contrast.