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IR SPECTROSCOPY. h86E.

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IR SPECTROSCOPY
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Page 1: IR SPECTROSCOPY.  h86E.

IR SPECTROSCOPY

Page 2: IR SPECTROSCOPY.  h86E.

• http://www.youtube.com/watch?v=DDTIJgIh86E

Page 3: IR SPECTROSCOPY.  h86E.

• Light is one form of electromagnetic radiation.

• Light is only a very small part of the electromagnetic spectrum.

• Electromagnetic waves consist of electric and magnetic fields which are perpendicular to each other and to the direction of travel of the wave.

• The electric and magnetic fields vibrate at the same frequency as each other.

Page 4: IR SPECTROSCOPY.  h86E.

THE ELECTROMAGNETIC SPECTRUM

Page 5: IR SPECTROSCOPY.  h86E.

Atoms, molecules and ions can absorb (or emit) electromagnetic radiation of specific frequencies, and this can be used to identify them.

Electromagnetic radiation absorbed

What the energy is used for

Spectroscopy technique

Ultra-violet / visibleMovement of electrons to higher energy levels

Ultra-violet / visible spectroscopy

Infra-red To vibrate bondsInfra-red

spectroscopy

Microwaves To rotate moleculesMicrowave

spectroscopy

Radio waves To change nuclear spin NMR spectroscopy

Page 6: IR SPECTROSCOPY.  h86E.

INFRA-RED SPECTROSCOPY

• All bonds vibrate at a characteristic frequency.

• There are different types of vibration.

Symmetric stretch Assymmetric stretch Bending

• The frequency depends on the mass of the atoms in the bond, the bond strength, and the type of vibration.

• The frequencies at which they vibrate are in the infra-red region of the electromagnetic spectrum.

Page 7: IR SPECTROSCOPY.  h86E.

INFRA-RED SPECTROSCOPY

• Wavenumbers (cm-1) are used as a measure of the wavelength or frequency of the absorption.

Wavenumber = 1 wavelength (cm)

• If IR light is passed through the compound, it will absorb some or all of the light at the frequencies at which its bonds vibrate.

• IR light absorbed is in the range 4000 – 400 cm-1.

• Above 1500 cm-1 is used to identify functional groups.

• Below 1500 cm-1 is used for fingerprinting.

Page 8: IR SPECTROSCOPY.  h86E.

BELOW 1500 cm-1 – “Fingerprinting”

• Complicated and contains many signals – picking out functional group signals difficult.

• This part of the spectrum is unique for every compound, and so can be used as a "fingerprint".

• This region can also be used to check if a compound is pure.

Page 9: IR SPECTROSCOPY.  h86E.

CH2 C

CH3

CH2 CH3

CH3 C CH

CH3

CH3

Page 10: IR SPECTROSCOPY.  h86E.

cyclohexane

C–H

Page 11: IR SPECTROSCOPY.  h86E.

cyclohexene

C–H

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butanal

C–H

CH2 CH2 C

O

HCH3

Page 13: IR SPECTROSCOPY.  h86E.

ethanoic acid

O–H

CH3 C

O

O H

Page 14: IR SPECTROSCOPY.  h86E.

ethanol

O–H

CH3 CH2 O H

Page 15: IR SPECTROSCOPY.  h86E.

butanal

C=O

CH2 CH2 C

O

HCH3

Page 16: IR SPECTROSCOPY.  h86E.

propanone

C=O

CH3 C

O

CH3

Page 17: IR SPECTROSCOPY.  h86E.

ethanoic acid

C=O

CH3 C

O

O H

Page 18: IR SPECTROSCOPY.  h86E.

methyl ethanoate

C=O

CH3 C

O

O CH3

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CH3 CH2 O H

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Page 31: IR SPECTROSCOPY.  h86E.

Task 1

Page 32: IR SPECTROSCOPY.  h86E.

Exercise 1

Match the following eight compounds to the following eight IR spectra.

hex-2-ene

pentane

methylpropan-1-ol

2-methylpentan-3-one

butanal

butanoic acid

propyl ethanoate

nitrobenzene

Page 33: IR SPECTROSCOPY.  h86E.

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C-O

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C=O

propyl ethanoate

CH3 C

O

O CH2 CH2 CH3

Page 42: IR SPECTROSCOPY.  h86E.

C=O

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2-methylpentan-3-one

CH3 CH C

O

CH2 CH3

CH3

Page 43: IR SPECTROSCOPY.  h86E.

methylpropan-1-ol

O-H

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CH3 CH CH2 OH

CH3

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C-H

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nitrobenzene NO2

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C-H

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pentane CH3 CH2 CH2 CH2 CH3

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C-H 10

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C=O

butanal CH3 CH2 CH2 C

O

H

Page 47: IR SPECTROSCOPY.  h86E.

O-H

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butanoic acid CH3 CH2 CH2 C

O

O H

Page 48: IR SPECTROSCOPY.  h86E.

C=C

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C-HC-H

hex-2-ene CH3 CH CH CH2 CH2 CH3

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F

Page 50: IR SPECTROSCOPY.  h86E.

G

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Page 54: IR SPECTROSCOPY.  h86E.

P

Page 55: IR SPECTROSCOPY.  h86E.

Q

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R

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S

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T

Page 59: IR SPECTROSCOPY.  h86E.

U


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