a beam of IR radiation is passed through a sample which is absorbed by the covalent bonds, increasing vibrational energy causing bond stretching or bending
bond stretching
bond length increases or decreases
bond bending
bond angle increases or decreases
what frequency of IR absorbed by a covalent bond depends on
atoms on either side of the bond
the position of the bond in a molecule
features of a single beam spectometer
radiation source
sample
detector
computer
printer
what molecules interact with IR
molecules that have their bonds stretched asymmetrically so change polarity
their absorptions are detected so an absorption spectrum can be produced
absorption spectrum
a plot showing how strongly a chemical absorbs radiation over a range of frequencies
transmittance
y-axis on an absorption spectrum
percentage radiation that passes through the sample
wavenumbers
x-axis on an absorption spectrum
400-1500 cm^-1
number of waves in 1cm
how hydrogen bonds affect peaks in absorption spectra
in alcohols, O-H peaks are more broad
even more broad in carboxylic acids because the O-H absorption overlaps with the C-H absorption
why are wavenumbers given as ranges?
the strength of a particular bond varies in different molecules due to atoms or groups around it so will absorb slightly different frequencies despite bonds being the same
fingerprint region
complex region of the absorption spectrum below 1500cm^-1 due to lots of single bonds stretching and bending vibrations unique to each molecule
so used to identify unknown compounds
how is a fingerprint region used to identify unkown compounds
comparing pattern in fingerprint region to that of recorded IR spectra in database
an exact match will identify the compound
way to interpret IR spectra
to predict absorptions in the spectrum of an organic compound
deduce functional groups in a compound from a list of wavenumbers
deduce the structure of a compound from wavenumbers and molecular formula