Organic Chemistry, 5th Edition

L. G. Wade, Jr.

Chapter 12
Infrared Spectroscopy and
Mass Spectrometry

Jo Blackburn
Richland College, Dallas, TX
Dallas County Community College District
2003,Prentice Hall
 Introduction
• Spectroscopy is an analytical technique
which helps determine structure.
• It destroys little or no sample.
• The amount of light absorbed by the
sample is measured as wavelength is
varied.

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Chapter 12 2
 Types of Spectroscopy
• Infrared (IR) spectroscopy measures the bond
vibration frequencies in a molecule and is used
to determine the functional group.
• Mass spectrometry (MS) fragments the molecule
and measures the masses.
• Nuclear magnetic resonance (NMR)
spectroscopy detects signals from hydrogen
atoms and can be used to distinguish isomers.
• Ultraviolet (UV) spectroscopy uses electron
transitions to determine bonding patterns. =>
Chapter 12 3
 Electromagnetic
Spectrum
• Examples: X rays, microwaves, radio
waves, visible light, IR, and UV.
• Frequency and wavelength are
inversely proportional.
• c = , where c is the speed of light.
• Energy per photon = h, where h is
Planck’s constant. =>
Chapter 12 4
The Spectrum and
Molecular Effects

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Chapter 12 5
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 The IR Region
• Just below red in the visible region.
• Wavelengths usually 2.5-25 m.
• More common units are wavenumbers,
or cm-1, the reciprocal of the wavelength
in centimeters.
• Wavenumbers are proportional to
frequency and energy. =>
Chapter 12 6
 Molecular Vibrations
Covalent bonds vibrate at only certain
allowable frequencies.

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Chapter 12 7
 Stretching Frequencies

• Frequency decreases with increasing

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Chapter 12 9
Fingerprint of Molecule
• Whole-molecule vibrations and bending
vibrations are also quantitized.
• No two molecules will give exactly the
same IR spectrum (except enantiomers).
• Simple stretching: 1600-3500 cm-1.
• Complex vibrations: 600-1400 cm-1,
called the “fingerprint region.”
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Chapter 12 10
 IR-Active and Inactive
• A polar bond is usually IR-active.
• A nonpolar bond in a symmetrical
molecule will absorb weakly or not at all.

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Chapter 12 11
 An Infrared
Spectrometer

Chapter 12 12 =>
 FT-IR Spectrometer
• Uses an interferometer.
• Has better sensitivity.
• Less energy is needed from source.
• Completes a scan in 1-2 seconds.
• Takes several scans and averages them.
• Has a laser beam that keeps the
instrument accurately calibrated. =>

Chapter 12 13
 Carbon-Carbon
Bond Stretching
• Stronger bonds absorb at higher
frequencies:
C-C 1200 cm-1
C=C 1660 cm-1
CC 2200 cm-1 (weak or absent if internal)
• Conjugation lowers the frequency:
isolated C=C 1640-1680 cm-1
conjugated C=C 1620-1640 cm-1
aromatic C=C approx. 1600 cm-1 =>
Chapter 12 14
 Carbon-Hydrogen
Stretching
Bonds with more s character absorb at a
higher frequency.
sp3 C-H, just below 3000 cm-1 (to the right)
sp2 C-H, just above 3000 cm-1 (to the left)
sp C-H, at 3300 cm-1

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Chapter 12 15
An Alkane IR Spectrum

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Chapter 12 16
An Alkene IR Spectrum

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Chapter 12 17
An Alkyne IR Spectrum

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Chapter 12 18
 O-H and N-H
Stretching
• Both of these occur around 3300 cm-1,
but they look different.
Alcohol O-H, broad with rounded tip.
Secondary amine (R2NH), broad with one
sharp spike.
Primary amine (RNH2), broad with two
sharp spikes.
No signal for a tertiary amine (R3N) =>
Chapter 12 19
An Alcohol IR
Spectrum

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Chapter 12 20
 An Amine
IR Spectrum

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Chapter 12 21
 Carbonyl Stretching
• The C=O bond of simple ketones,
aldehydes, and carboxylic acids absorb
around 1710 cm-1.
• Usually, it’s the strongest IR signal.
• Carboxylic acids will have O-H also.
• Aldehydes have two C-H signals around
2700 and 2800 cm-1.
=>
Chapter 12 22
 A Ketone
IR Spectrum

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Chapter 12 23
An Aldehyde
IR Spectrum

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Chapter 12 24
 O-H Stretch of a
Carboxylic Acid
This O-H absorbs broadly, 2500-3500 cm-1,
due to strong hydrogen bonding.

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Chapter 12 25
 Variations in
C=O Absorption
• Conjugation of C=O with C=C lowers the
stretching frequency to ~1680 cm-1.
• The C=O group of an amide absorbs at an
even lower frequency, 1640-1680 cm-1.
• The C=O of an ester absorbs at a higher
frequency, ~1730-1740 cm-1.
• Carbonyl groups in small rings (5 C’s or
less) absorb at an even higher frequency. =>
Chapter 12 26
 An Amide
IR Spectrum

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Chapter 12 27
 Carbon - Nitrogen
Stretching
• C - N absorbs around 1200 cm-1.
• C = N absorbs around 1660 cm-1 and is
much stronger than the C = C
absorption in the same region.
• C  N absorbs strongly just above 2200
cm-1. The alkyne C  C signal is much
weaker and is just below 2200 cm-1 .
=>
Chapter 12 28
 A Nitrile
IR Spectrum

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Chapter 12 29
Summary of IR
Absorptions

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Chapter 12 30
 Strengths and Limitations
• IR alone cannot determine a structure.
• Some signals may be ambiguous.
• The functional group is usually indicated.
• The absence of a signal is definite proof
that the functional group is absent.
• Correspondence with a known sample’s
IR spectrum confirms the identity of the
compound. =>
Chapter 12 31
 Mass Spectrometry
• Molecular weight can be obtained from a
very small sample.
• It does not involve the absorption or
emission of light.
• A beam of high-energy electrons breaks
the molecule apart.
• The masses of the fragments and their
relative abundance reveal information
about the structure of the molecule. =>

Chapter 12 32
 Electron Impact Ionization
A high-energy electron can dislodge an
electron from a bond, creating a radical
cation (a positive ion with an unpaired e-).
H H
H C C H
H H
H H H H
e- + H C C H H C C+ H
H H H H
H H
H C+ C H
Chapter 12 =>
33
H H
 Separation of Ions
• Only the cations are deflected by the
magnetic field.
• Amount of deflection depends on m/z.
• The detector signal is proportional to the
number of ions hitting it.
• By varying the magnetic field, ions of all
masses are collected and counted. =>

Chapter 12 34
Mass Spectrometer

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Chapter 12 35
 The Mass Spectrum
Masses are graphed or tabulated according to
their relative abundance.

Chapter 12 36 =>
 The GC-MS
A mixture of compounds is separated
by gas chromatography, then identified
by mass spectrometry.

Chapter 12 37
=>
 High Resolution MS
• Masses measured to 1 part in 20,000.
• A molecule with mass of 44 could be
C3H8, C2H4O, CO2, or CN2H4.
• If a more exact mass is 44.029, pick the
correct structure from the table:
C3H8 C2H4O CO2 CN2H4
44.06260 44.02620 43.98983 44.03740
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Chapter 12 38
 Molecules with
Heteroatoms
• Isotopes: present in their usual abundance.
• Hydrocarbons contain 1.1% C-13, so there
will be a small M+1 peak.
• If Br is present, M+2 is equal to M+.
• If Cl is present, M+2 is one-third of M+.
• If iodine is present, peak at 127, large gap.
• If N is present, M+ will be an odd number.
• If S is present, M+2 will be 4% of M+. =>
Chapter 12 39
Isotopic Abundance

81
Br

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Chapter 12 40
Mass Spectrum
with Sulfur

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Chapter 12 41
Mass Spectrum
with Chlorine

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Chapter 12 42
Mass Spectrum
with Bromine

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Chapter 12 43
 Mass Spectra
of Alkanes
More stable carbocations will be more
abundant.

Chapter 12 44
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 Mass Spectra
of Alkenes
Resonance-stabilized cations favored.

Chapter 12 45
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 Mass Spectra
of Alcohols
• Alcohols usually lose a water molecule.
• M+ may not be visible.

Chapter 12 46
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End of Chapter 12

Chapter 12 47