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Infrared (IR) Spectroscopy allows the identification of particular bonds present within
molecules. In this class we have simplified IR analysis by only focusing on 5 regions of the
spectrum. Do not try to examine and identify each and every peak within the entire spectrum.
Instead, sequentially look at each of the designated 5 regions. Yes, you are expected
memorize the exact location for each of these regions and to know the distinctive peak shape
for the N-H/O-H region. First determine if there is a substantial absorbance present in each of
the designated regions. Then determine which bonds are present. From the bonds present,
determine which functional group is responsible. That is the functional group of the molecule.
You need to know your functional groups to be able to do this successfully.
Also review your lecture notes and read Klein text book.
N-H/OH Bonds. This is toward the far left of the spectra.(3200-3600 cm-1)
The shape and location define which bond type is present.
-O-H 3200-3600 cm-1 Alcohol; Broad, rounded and distinct
-NH2 3200-3600 cm-1 Primary Amine; Sharp double point
-N-H 3200-3600 cm-1 Secondary Amine; Sharp single point
-COO-H 2500-3600 cm-1 Carboxylic Acid; Very broad. Extends outside designated region.
CH Bonds The exact location defines the type of C-H bond present. (2800-
3100 cm-1) Draw a line at 3000 cm-1, peaks just to right are sp3 to left are sp2.
sp3-C-H 2800-3000 cm-1 sp3 Carbon-Hydrogen; Multi-peaked, strong. Almost always present
sp2-C-H 3000-3100 cm-1 sp2 Carbon-Hydrogen; Usually a shoulder on left of sp3 C-H
absorbance.
sp-C-H 3300 cm-1 Terminal Alkyne: Icicle-like within typical ‘NH/OH’ region
Double Bonds Two types of bonds overlap. The shape and exact location
defines which bond is present. (1600-1800 cm-1)
C=O 1650-1800 cm-1 Carbonyl; Strong distinct absorbance.
C=C 1600-1680 cm-1 Alkene; Sharp medium size
Fingerprint Region This area is used to confirm identity but is not very useful
for assigning identity.
C-O 1000-1300cm-1. This area is difficult to distinguish. Use only when necessary.
This area will be necessary to distinguish between an alkane and an ether, and between a
ketone and an ester.
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Bonds Position (cm-1) strength and Shape
O-H/ NH 3200-3600
(Hydrogen bonded to Nitrogen & Oxygen)
-O-H 3200-3600 rounded
-N-H, -NH2 3200-3600 single or double pointed
-COOH 2500-3600 very broad
≡ 2100-2300
(Triple Bond; Carbon to carbon and carbon to nitrogen)
C≡N 2100-2300 sharp
C≡C-H 2100-2300 sharp
= 1600-1800
(Double Bond; Carbon to )
C=O 1650-1800 strong slightly rounded
C=C 1600-1680 medium , sharp
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3200-3600cm-1 Oxygen-hydrogen, nitrogen-hydrogen (and
sp hybridized carbon-hydrogen bonds). Shape dependent.
Include Alcohols, Carboxylic Acids, Amines, Terminal Alkynes.
ALCOHOLS have very distinctive broad rounded absorbance between 3200 and 3600 cm-1.
There is a distinct break between the –OH absorbance and the sp3CH absorbance.
CARBOXYLIC ACID- The –OH of a carboxylic acid maximum absorbance shifts over
toward 3000cm-1. This is a very broad absorbance extending from 2500 to 3500cm-1 which
spills over the sp3CH absorbance.
TERMINAL ALYKNES- The terminal C-H bond of ≡C-H has a very sharp ‘icicle’ like
absorbance around 3300cm-1 .
PRIMARY AMINES- Show TWO short pointed absorbances between 3200-3600 cm-1.
SECONDARY AMINES- Shows one short pointed absorbance between 3200-3500 cm-1.
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Pattern differences between Carboxylic Acids, Alcohols,
Terminal Alkynes and Amines
Page 5
3100-3000cm-1 3000-2800cm-1. Sp2 and sp3 carbon-
hydrogen bonds.
Almost every organic molecule will have an absorbance in the 3000-2800cm-1 region
because most organic molecules contain sp3 C-H bonds. Different alkanes have little
discernible difference in this area. It is often useful to draw a vertical line at 3000cm-1, any
peak to the left of this line will be sp2 C-H bonds and those to the right will be sp3 C-H bonds.
If alkene =C-H is present it will often look like shoulder to left of a regular sp3 –C-H
absorbance around 3100.
Sp2 C-H
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1600-1680 cm-1 &1650-1800cm-1 Double Bond region, Carbonyl
(C=O) and Alkene (C=C)
Carbon-Oxygen double bond (C=O or carbonyl) has a very distinctive and strong absorbance
between1650-1800 cm-1 A “normal” ketone typically exists close to 1720 cm-1.
Carbon-Carbon double bonds, (C=C or alkene), absorb between 1600 and 1680cm-1.
Alkenes tend to be sharper and less intense (weaker) than carbonyl.
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Alkane. Only sp3 C-H at 2800-3000cm-1.
[ ] 3200-3600cm-1(O--H,N-H)
[ ] 3000-3100 cm-1(=C-H)
[X] 2800-3000 cm-1(C-H)
[ ] 2100-2300 cm-1 (≡)
[ ] 1650-1800 cm-1(C=O)
[ ]1600-1680 cm-1(C=C)
[ ] 1000-1300 cm-1(C-O)
Alkene . Sp2 C-H at 3100 cm-1, sp3 C-H at 2800-3000cm-1, C=C at 1620cm-`.
[ ] 3200-3600cm-1(O--H,N-H)
[X ] 3000-3100 cm-1(=C-H)
[X] 2800-3000 cm-1(C-H)
[ ] 2100-2300 cm-1 (≡)
[ ] 1650-1800 cm-1(C=O)
[X ]1600-1680 cm-1(C=C)
[ ] 1000-1300 cm-1(C-O)
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Carboxylic Acid . VERY BROAD –-O-H which spills over into normal sp3 C-H at 2800-3000cm-
1
region, C=O at 1710cm-1,
[X] 3200-3600cm-1(O--H,N-H)
[ ] 3000-3100 cm-1(=C-H)
[X] 2800-3000 cm-1(C-H)
[ ] 2100-2300 cm-1 (≡)
[X ] 1650-1800 cm-1(C=O)
[ ]1600-1680 cm-1(C=C)
[x ] 1000-1300 cm-1(C-O)
[ ] 3200-3000cm-1(O--H,N-H)
[ ] 3000-3100 cm-1(=C-H)
[X] 2800-3000 cm-1(C-H)
[X ] 2100-2300 cm-1 (≡)
[ ] 1650-1800 cm-1(C=O)
[ ]1600-1680 cm-1(C=C)
[ ] 1000-1300 cm-1(C-O)
terminal alkyne Sp C-H at 3300cm-1, sp3 C-H at 2800-3000cm-1, C≡C or C≡N at 2250cm-1,
[X] 3200-3600cm-1(O--H,N-H)
[ ] 3000-3100 cm-1(=C-H)
[X] 2800-3000 cm-1(C-H)
[X ] 2100-2300 cm-1 (≡)
[ ] 1650-1800 cm-1(C=O)
[ ]1600-1680 cm-1(C=C)
[ ] 1000-1300 cm-1(C-O)
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Ketone or Aldehyde , sp3 C-H at 2800-3000cm-1, C=O at 1720 cm-1,
[ ] 3200-3600cm-1(O--H,N-H)
[ ] 3000-3100 cm-1(=C-H)
[X] 2800-3000 cm-1(C-H)
[ ] 2100-2300 cm-1 (≡)
[X ] 1650-1800 cm-1(C=O)
[ ]1600-1680 cm-1(C=C)
[ ] 1000-1300 cm-1(C-O)
[ ] 3200-3600cm-1(O--H,N-H)
[ ] 3000-3100 cm-1(=C-H)
[X] 2800-3000 cm-1(C-H)
[ ] 2100-2300 cm-1 (≡)
[X ] 1650-1800 cm-1(C=O)
[ ]1600-1680 cm-1(C=C)
[X ] 1000-1300 cm-1(C-O)
[X] 3200-3600cm-1(O--H,N-H)
[ ] 3000-3100 cm-1(=C-H)
[X] 2800-3000 cm-1(C-H)
[ ] 2100-2300 cm-1 (≡)
[X ] 1650-1800 cm-1(C=O)
[ ]1600-1680 cm-1(C=C)
[ ] 1000-1300 cm-1(C-O)
[ ] 3200-3600cm-1(O--H,N-H)
[ ] 3000-3100 cm-1(=C-H)
[X] 2800-3000 cm-1(C-H)
[ ] 2100-2300 cm-1 (≡)
[ ] 1650-1800 cm-1(C=O)
[ ]1600-1680 cm-1(C=C)
[X ] 1000-1300 cm-1(C-O)
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Infrared chemical bond absorbance regions by functional group
CnH(2n+2)
Alkane Alkene Terminal alkyne
-1
[ ] 3200-3600cm (O-H,N-H) [ ] 3200-3600cm-1(O-H,N-H) [X] 3300cm-1(≡C-H)
-1
[ ] 3000-3100 cm (=C-H) [X] 3000-3100 cm-1(=C-H) [ ] 3000-3100 cm-1(=C-H)
-1
[X] 2800-3000 cm (C-H) [X] 2800-3000 cm-1(C-H) [X ] 2800-3000 cm-1(C-H)
[ ] 2100-2300 cm-1 (≡) [ ] 2100-2300 cm-1 [X] 2100-2300 cm-1(C≡C)
-1
[ ] 1650-1800 cm (C=O) [ ] 1650-1800 cm-1(C=O) [ ] 1650-1800 cm-1(C=O)
[ ]1600-1680 cm-1(C=C) [X ]1600-1680 cm-1(C=C) [ ]1600-1680 cm-1(C=C)
-1
[ ] 1000-1300 cm (C-O) [ ] 1000-1300 cm-1(C-O) [ ] 1000-1300 cm-1(C-O)
or
and
Ketone and aldehydes Ester Carboxylic Acid
[ ] 3200-3600cm-1(O-H) [ ] 3200-3600cm-1(O-H) [X]3200-3600cm-1(COO-H)
[X] 2800-3100 cm-1(C-H) [X] 2800-3100 cm-1(C-H) [X] 2800-3100 cm-1(C-H)
[ ] 2100-2300 cm-1(C≡N, C≡C) [ ] 2100-2300 cm-1(≡) [ ] 2100-2300 cm-1(≡)
[X ] 1650-1800 cm-1(C=O) [X] 1650-1800 cm-1(C=O) [X] 1650-1800 cm-1(C=O)
[ ]1600-1680 cm-1 (C=C) [ ]1600-1680 cm-1(C=C) [ ]1600-1680 cm-1(C=C)
[ ] 1000-1300 cm-1(C-O) [X] 1000-1300 cm-1(C-O) [X] 1000-1300 cm-1(C-O)
Amine Amide
[X] 3200-3600cm-1(N-H) [X] 3200-3600cm-1(N-H)
[X] 2800-3100 cm-1(C-H) [X] 2800-3100 cm-1(C-H)
[ ] 2100-2300 cm (≡)
-1 [ ] 2100-2300 cm-1(≡)
[ ] 1650-1800 cm-1(C=O) [X] 1650-1800 cm-1(C=O)
-1
[ ]1600-1680 cm (C=C) [ ]1600-1680 cm-1(C=C)
[ ] 1000-1300 cm-1(C-O) [ ] 1000-1300 cm-1(C-O)
Revised November 13, 2019s.l. weaver
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