3. ir lecturer

8/13/2019 3. IR Lecturer

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Infrared Spectroscopy

I. Infrared SpectroscopyA. Energy Absorption and Vibration

1) IR electromagnetic radiation is just less energetic than visible light

2) This energy is sufficient to cause excitation of vibrational energy levels

3) Wavelength (

) = 2.5-16.7 x 10

-6

m

kcal/mol101cm4000-6001~ 1

===

hchc

hE

1

m/s10x3.0c 8

===

=

==

4) = wavenumbers. Larger = higher energy

5) Excitation depends on atomic mass and how tightly they are bound

a) Hookes Law for 2 masses connected by a spring

b) CH Bond: Reduced Mass = (12+1)/(12x1) = 13/12 = 1.08

c) CC Bond: Reduced Mass = (12+12)/(12x12) = 24/144 = 0.167

21

21 )(~mm

mmfk += k = constantf = force constant = bond strengthm-term = reduced mass

sx.onstantsanc - ==


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Vibrational modes leading to IR absorptions:

Many possible absorptions per molecule exist: stretching, bending,


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B. Using IR in Organic Chemistry

1. Functional Groups have characteristic IR absorptions

2. Fingerprint Region (600-1500 cm-1) is unique for every molecule and letsus match an unknown with a known spectrum


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Regions of the Infrared Spectrum

I. 4000-2500 cm-1 N-H,C-H, O-H (stretching)

A. 3300-3600 N-H, O-H

B. 3000 C-H

II. 2500-2000 cm-1 CC and C N(stretching)

I. 2000-1500 cm-1 double bonds(stretching)

A. C=O 1680-1750

B. C=C 1640-1680 cm-1

II. Below 1500 cm-1 fingerprintregion


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12.8 Infrared Spectra of Some Common Functional Groups

Alkanes, Alkenes, Alkynes

I. C-H, C-C, C=C, C C have characteristic peaks

A. absence helps rule out C=C or C C


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4. IR of Alkenes

a. Alkene CH absorbs at higher energy than alkanes because theforce constant is stronger than alkanes (sp2 hybridization)

b. Substitution pattern of alkenes give characteristic absorptions

i. Terminal alkenes give 910, 990 cm-1

C C

R

H

H

H

ii. Geminal disubstituted gives 890 cm-1

iii. trans disubstituted gives 970 cm-1

C C

R

H

H

R

C C

H

H

R

R


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IR: Aromatic Compounds

I. Weak CH stretch at 3030 cm1

II. Weak absorptions 1660 - 2000 cm1 range

III. Medium-intensity absorptions 1450 to 1600 cm1


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IR: Alcohols and Amines

I. OH 3400 to 3650 cm1

A. Usually broad and intense

II. NH 3300 to 3500 cm1

A. Sharper and less intense than an OH


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IR: Carbonyl Compounds

I. Strong, sharp C=O peak 1670 to 1780 cm1

II. Exact absorption characteristic of type of carbonyl compound

A. 1730 cm1 in saturated aldehydes

B. 1705 cm1 in aldehydes next to double bond or aromatic ring


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C=O in Ketones

I. 1715 cm1

in six-membered ring and acyclic ketonesII. 1750 cm1 in 5-membered ring ketones

III. 1690 cm1 in ketones next to a double bond or an aromatic ring

I. 1735 cm1 in saturated esters

II. 1715 cm1 in esters next to aromatic ring or a double bond

C=O in Esters


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3. ir lecturer

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