Table For FTIR

Spectroscopy Data Tables
Infrared Tables (short summary of common absorption frequencies)

The values given in the tables that follow are typical values. Specific bands may fall over a range of
wavenumbers, cm-1. Specific substituents may cause variations in absorption frequencies. Absorption
intensities may be stronger or weaker than expected, often depending on dipole moments. Additional
bands may confuse the interpretation. In very symmetrical compounds there may be fewer than the
expected number of absorption bands (it is even possible that all bands of a functional group may
disappear, i.e. a symmetrically substituted alkyne!). Infrared spectra are generally informative about what
functional groups are present, but not always. The 1H and 13C NMRs are often just as informative about
functional groups, and sometimes even more so in this regard. Information obtained from one
spectroscopic technique should be verified or expanded by consulting the other spectroscopic techniques.
IR Summary - All numerical values in the tables below are given in wavenumbers, cm-1
Bonds to Carbon (stretching wave numbers)
sp3 C-X single bonds
sp2 C-X single bonds

C
C
C
1050-1150
alkoxy C-O
1000-1350
not very useful
not used
sp2 C-X double bonds
1600-1680
not very useful
1640-1810
expanded table
on next page
1640-1690
1100-1350
acyl and phenyl C-O
1250
2100-2250
2240-2260
Stronger dipoles produce more intense IR bands and weaker dipoles produce less intense IR bands (sometimes none).
Bonds to Hydrogen (stretching wave numbers)

C
H
C
3000-3100
sp3 C-H
(see sp2 C-H bend
patterns below)
2850-3000
sp3 C-H
2700-2760
2800-2860
aldehyde C-H
(two bands)
3300
sp3 C-H
(sp C-H bend 620)
H
C
O
C
3100-3500
primary NH2
(two bands)
3100-3500
secondary N-H
(one band)
amides = strong, amines = weak
Z:\files\classes\spectroscopy\typical spectra charts.DOC
sp C-X triple bonds

C
3200-3400
2500-3400
alcohol O-H
acid O-H
2550 -2620
(very weak)
thiol S-H
Carbonyl Highlights (stretching wave numbers)

Aldehydes
Ketones
Esters
Acids
O
C
H
saturated = 1725
conjugated = 1690
aromatic = 1700
Anhydrides
Amides
saturated = 1715
conjugated = 1690
aromatic = 1690
nitro
Acid Chlorides
O
NR2
saturated = 1650
conjugated = 1660
aromatic = 1660
6 atom ring = 1670
5 atom ring = 1700
4 atom ring = 1745
3 atom ring = 1850
saturated = 1760, 1820

conjugated = 1725, 1785
aromatic = 1725, 1785
6 atom ring = 1750, 1800
5 atom ring = 1785, 1865
alkene substitution
pattern
Cl
saturated = 1800
conjugated = 1770
aromatic = 1770
N
O
asymmetric = 1500-1600
symmetric = 1300-1390
Very often there is a very weak C=O overtone at approximately 2 x (3400 cm-1).
Sometimes this is mistaken for an OH or NH peak.,
sp2 C-H bend patterns for alkenes

descriptive
alkene term
sp2 C-H bend patterns for aromatics
absorption
frequencies (cm-1)
due to sp2 CH bend
descriptive
aromatic term
aromatic substitution
pattern
absorption
frequencies (cm-1)
due to sp2 CH bend
H
C
monosubstituted
alkene
R
C
H
C
H
C
R
C
R
C
monosubstituted
aromatic
675-730
(broad)
ortho disubstituted
aromatic
trans disubstituted
alkene
960-990
geminal disubstituted
alkene
880-900
trisubstituted
alkene
790-840
tetrasubstituted
alkene
985-1000
900-920
690-710
730-770
cis disubstituted
alkene
saturated = 1735
conjugated = 1720
aromatic = 1720
6 atom ring = 1735
5 atom ring = 1775
4 atom ring = 1840
saturated = 1715
conjugated = 1680
aromatic = 1690
6 atom ring = 1715
5 atom ring = 1745
4 atom ring = 1780
3 atom ring = 1850
R'
none
735-770
meta disubstituted
aromatic
para disubstituted
aromatic
680-725
750-810
880-900 (sometimes)
790-840
Aromatic compounds have characteristic weak overtone bands

that show up between 1650-2000 cm-1). Some books provide
pictures for comparison (not here). A strong C=O peak will
cover up most of this region.
3
units = cm-1
4000
2500
3000
3500
sp C-H
stretch
1700
2000
sp3 C-H
stretch
C C
thiol S-H
stretch
sp2 C-H
stretch
1500 1400 1300 1200 1100 1000 900 800 700
C=O
stretch
aldehyde C-H
stretch
geminal
acyl C-O
phenol C-O
tri
aromatic sp2 C-H

bend
mono
N-H bend
ortho
2o N-H
stretch
nitro
meta
nitro
para
3000
2500
1700
2000
1500 1400 1300 1200 1100 1000 900
expansion of alkene & aromatic sp2 C-H bend region (units = cm-1)
700
600
800
900
mono
cis
trans
C=C stretch
aromatic
1o N-H2
stretch
1000
mono
alkoxy C-O
carboxylic acid O-H

stretch
3500
sp C-H
bend
C=C stretch
alkene
alcohol O-H
stretch
4000
alkene sp2 C-H

bend
C=N
stretch
C N
600 500
800 700
600 500
500
mono
cis
alkene sp2 C-H

bend
trans
geminal
tri
mono
mono
aromatic sp2 C-H

bend
ortho
meta
meta
meta
para
1750
1800
Saturated C=O lies at

higher cm-1
C=O in samll rings
lies at higher cm-1
expansion of carbonyl (C=O) stretch region (units = cm-1)

1700
1650
carboxylic acid C=O (also acid "OH")

ester C=O (also acyl C-O and alkoxy C-O)
aldehyde C=O (also aldehyde C-H)
ketone C=O (nothing special)
acid chloride C=O (high C=O, 1 peak)

anhydride C=O
anhydride C=O (high C=O, 2 peaks)
amide C=O (low C=O, amide N-H)
1600
Conjugated C=O
lies at lower cm-1
IR Flowchart to determine functional groups in a compound (all values in cm-1).

IR Spectrum
has C=O band

(1650-1800 cm-1)
very strong
does not have

C=O band
C
aldehydes
O
1725-1740 (saturated)
1660-1700 (unsaturated)
C
sometimes lost
2860-2800
in sp3 CH peaks
2760-2700
aldehyde C-H
(both weak)
ketones
1715-1810 (rings: higher
in small rings)
esters - rule of 3
O
1735-1820 (higher in small rings)
acyl
O
1150-1350 (acyl, strong)
alkoxy
(1000-1150, alkoxy, medium)
acids
O
1680-1700 (higher in small rings)
acyl
C
2400-3400, very broad

(overlaps C-H stretch)
acid
O
nitriles
C
a little lower
when conjugated
2150
(variable intensity)
not present or weak when symmetrically
substituted, a little lower when conjugated
C
sp C-H stretch
sp C-H bend
3300
sharp, strong
620
All IR values are approximate and have a range

of possibilities depending on the molecular
environment in which the functional group resides.
Resonance often modifies a peak's position
because of electron delocalization (C=O lower,
acyl C-O higher, etc.). IR peaks are not 100%
reliable. Peaks tend to be stronger (more intense)
when there is a large dipole associated with a
vibration in the functional group and weaker in
less polar bonds (to the point of disappearing in
some completely symmetrical bonds).
1460 & 1380
sp3 C-H bend

C
not useful
alkenes
sp2 C-H stretch
3000-3100
650-1000
(see table for
spectral patterns)
sp2 C-H bend

C
1600-1660
weak or not present
aromatics
sp2 C-H stretch
3050-3150
690-900 (see table),
overtone patterns
between 1660-2000
sp2 C-H bend

C
1600 & 1480

can be weak
alcohols
alcohol
O
3600-3500
1000-1260
(3o > 2o > 1o)
2550 (weak)
(easy to overlook)
alkoxy
C
Alkene sp C-H bending patterns
amines
1745 (in 4 atom ring)
C
H
N
o
N
H
2o
3350 & 3180, two bands

for 1o amides,
one band for 2o amides,
H stronger than in amines, extra
overtone sometimes at 3100
N-H bend, 1550-1640,

stronger in amides than amines
acid chlorides
1800 (saturated)
1770 (unsaturated)
Inductive pull of Cl increases the

electron density between C and O.
anhydrides
O
1760 & 1820 (saturated)

two strong bands
acyl
C
2850-3000
thiols
thiol
amides
alkanes
sp3 C-H stretch
alkynes
2250
sharp, stronger
than alkynes,
monosubstituted alkene (985-1000, 900-920)

geminal disubstituted (960-990)
cis disubstituted (675-730)
trans disubstituted (880-900)
trisubstituted (790-840)
tetrasubstituted (none, no sp2 C-H)
Aromatic sp2 C-H bending patterns

monosubstituted (730-770, 690-710)
ortho disubstituted (735-770)
meta disubstituted (880-900,sometimes,
750-810, 680-725)
para disubstituted (790-840)
H
N
N
1o
2o
N-H bend, 1550-1640,

stronger in amides than amines
1000-1350
(uncertain)
ethers
alkoxy
C
1120 (alphatic)
1040 & 1250 (aromatic)
nitro compounds
O
1500-1600, asymmetric (strong)

1300-1390, symmetric (medium)
There are also weak overtone bands between

1660 and 2000, but are not shown here. You
can consult pictures of typical patterns in other
reference books. If there is a strong C=O band,
they may be partially covered up.
3300 - 3500, two bands

for 1o amines, one band
o
H for 2 amines, weaker
than in amides,
carbon-halogen bonds

X = F, Cl, Br, I
usually not
very useful
5
Typical 1H and 13C NMR chemical shift values.
deshielding side = less electron rich

(inductive & resonance)
shielding side = more electron rich

(inductive & resonance)
typical proton chemical shifts
amine N-H
Carbon and/or heteroatoms without hydrogen do

not appear here, but influence on any nearby protons
may be seen in the chemical shifts of the protons.
alcohol
1
amide N-H
S C H
thiols, sulfides
2.5
N
3.0
X C H
X = F,Cl,Br,I
10
8+
6
7
PPM
alcohols
ethers
esters
5+
5
ketones
no H
15
N C
amines, amides
with & without H
180
50
O
O
C
180
C C
with & without H
N C
no H
90
70
40
S
thiols, sulfides
with & without H
160
O
C
60
-
110
125
30
epoxides
with & without H
carboxylic acids
anhydrides
esters
amides
acid chlorides
no H
alcohols,
ethers, esters
40
20
with & without H

H
aldehydes
with H
200
F 80-95
Cl 45-70
Br 35-65
I 15-45
220+
220
95
210
0.5
with & without H
halogen
simple sp3 C-H

CH > CH2 > CH3
3.3 3
typical carbon-13 chemical shifts
240
1.5 1.3
2.5
3.5
H
O C
aromatic C-H
10
thiol
SH
epoxide C-H
10
11
1.5
3+
7+
aldehyde C-H
12
2.5
benzylic C-H
carbonyl alpha C-H
alkene C-H
12
2.3
allylic C-H
carboxylic acid O-H
2.0
C H
amines
80
50
with & without H

180
180
160+
160
100-
140 PPM 120
100
simple sp3 carbon

C > CH > CH2 > CH3
with & without H
60+
80
60
40
20
6
Calculation of chemical shifts for protons at sp3 carbons
H
C C C
Estimation of sp3 C-H chemical shifts with multiple substituent parameters for protons within 3 C's of consideration.
= directly attached substituent, use these values when the hydrogen and substituent are attached to the same carbon
= once removed substituent, use these values when the hydrogen and substituent are on adjacent (vicinal) carbons
= twice removed substituent, use these values when the hydrogen and substituent have a 1,3 substitution pattern
0.0
0.8
0.9
1.4
3.2
2.2
2.1
2.0
2.3
2.1
1.5
2.5
2.8
2.8
3.1
2.8
1.5
2.1
3.2
1.3
1.3
1.1
1.2
1.7
1.1
1.1
1.0
1.8
1.1
1.6
1.8
X = substituent
R- (alkyl)
R2C=CR- (alkenyl)
RCC- (alkynyl)
Ar- (aromatic)
F- (fluoro)
Cl- (chloro)
Br- (bromo)
I- (iodo)
HO- (alcohol)
RO- (ether)
epoxide
R2C=CRO- (alkenyl ether)
ArO- (aromatic ether)
RCO2- (ester, oxygen side)
ArCO2- (aromatic ester, oxygen side)
ArSO3- (aromatic sulfonate, oxygen)
H2N- (amine nitrogen)
RCONH- (amide nitrogen)
O2N- (nitro)
HS- (thiol, sulfur)
RS- (sulfide, sulfur)
OHC- (aldehyde)
RCO- (ketone)
ArCO- (aromatic ketone)
HO2C- (carboxylic acid)
RO2C- (ester, carbon side)
H2NOC- (amide, carbon side)
ClOC- (acid chloride)
NC- (nitrile)
RSO- (sulfoxide)
RSO2- (sulfone)
0.0
0.2
0.3
0.4
0.5
0.5
0.7
0.9
0.3
0.3
0.4
0.4
0.5
0.5
0.5
0.4
0.2
0.3
0.8
0.4
0.4
0.4
0.3
0.3
0.3
0.3
0.3
0.4
0.4
0.5
0.5
0.0
0.1
0.1
0.1
0.2
0.2
0.2
0.1
0.1
0.1
0.1
0.2
0.3
0.1
0.2
0.0
0.1
0.1
0.1
0.1
0.1
0.1
0.0
0.1
0.1
0.1
0.1
0.1
0.2
0.3
0.3
Starting value and equations for CH3's
CH3 = 0.9 +
H3C
CH3 = 0.9 + ( + )
H3C C C
is the summation symbol for all substituents considered

Starting value and equation for CH2's
In a similar manner we can calculate chemical shifts
for methylenes (CH2) using the following formula
CH2 = 1.2 + ( + + )
H
H C C C

Starting value and equation for CH's
In a similar manner we can calculate chemical shifts
for methines (CH) using the following formula
CH = 1.5 + ( + + )
H
C C C
a. methine b. methylene
d. methyl
H3C
CH2
CH3
HO
N
CH
O
H2C
H2C
e. methylene
f. methylene
c. methyl
Calculations are generally close to

actual chemical shifts for a single
substituent, but are less reliable as
the number of substituent factors
goes up. Multiple substituent factors
tend to overestimate an actual chemical
shift.
a. methine = 1.5 + (1.4) + (2.3) + (0.2) = 5.4 ppm

actual = 5.2
d. methyl = 0.9 + (0.1) = 1.0 ppm

actual = 1.0
b. methylene = 1.2 + (1.5) + (0.4) + (0.3) = 3.4 ppm

actual = 3.0 and 3.2
e. methylene = 1.2 + (0.3) = 1.5 ppm

actual = 1.7
c. methyl = 0.9 + (1.5) = 2.4 ppm

actual = 2.6
f. methylene = 1.2. + (1.7) = 2.9 ppm

actual = 2.9

Estimated chemical shifts for protons at alkene sp2 carbons
Substituent
HHydrogen
RAlkyl
C6H5CH 2Benzyl
X-CH2Halomethyl
(H)/ROCH2alkoxymethyl
(H)2/R2NCH2aminomethyl
RCOCH2-keto
NCCH2-cyano
R2C=CRAlkenyl
C6H5Phenyl
FFluoro
ClChloro
BrBromo
IIodo
ROakoxy (ether)
RCO2O-ester
(H)2/R2NN-amino
RCONHN-amide
O2NNitro
RSThiol
OHCAldehyde
ROCKetone
HO2CC-acid
RO2CC-ester
H2NOCC-amide
NCNitrile
geminal
cis
trans
0.0
0.0
0.0
0.5
-0.2
-0.3
0.7
-0.2
-0.2
0.7
0.1
0.0
0.6
0.0
0.0
0.6
-0.1
-0.1
Substitution relative to calculated "H"

cis
H
C C
trans
gem
(ppm) = 5.2 + gem + cis + trans

Example Calculation
gem
H
C
0.7
-0.1
-0.1
0.7
-0.1
-0.1
1.2
0.0
0.0
1.4
0.4
-0.1
1.5
-0.4
-1.0
trans = 5.2 - 0.1 = 5.1

actual = 5.1
1.1
0.2
0.1
1.1
0.4
0.6
cis = 5.2 + 0.4 = 5.7

actual = 5.6
1.1
0.8
0.9
1.2
-1.1
-1.2
2.1
-0.4
-0.6
0.8
-1.3
-1.2
2.1
-0.6
-0.7
1.9
1.3
0.6
1.1
-0.3
-0.1
1.0
1.0
1.2
1.1
0.9
0.7
0.8
1.0.
03
0.8
1.0
0.5
0.4
1.0
0.5
0.3
0.8
0.6
trans
H
cis
CH3O
gem = 5.2 + 1.4 = 6.6

actual = 6.6
bH
C
aH
c
d
H H
C
C
O C
O
e
H
C
Hf
a = 5.2 + (-0.4) = 4.8

actual = 4.9 (J = 14, 1.6 Hz)
b = 5.2 + (-0.6) = 4.6
actual = 4.6 (J = 6, 1.6 Hz)
c = 5.2 + 2.1 = 7.3
actual = 7.4 (J = 14, 6 Hz)
d = 5.2 + 0.8 = 6.0
actual = 6.2 (J = 18, 11 Hz)
e = 5.2 + 0.5 = 5.7
actual = 5.8 (J = 11, 1.4 Hz)
f = 5.2 + 1.0 = 6.2
actual = 6.4 (J = 18, 1.4 Hz)

Estimated chemical shifts for protons at aromatic sp2 carbons
Substituent
HHydrogen
CH3Methyl
ClCH2Cholromethyl
Cl3CHalomethyl
HOCH 2Hydroxymethyl
R2C=CRAlkenyl
C6H5Phenyl
FFluoro
ClChloro
BrBromo
IIodo
HOHydroxy
ROAlkoxy
RCO 2O-ester
(H)2/R2NN-amino
RCONHN-amide
O 2NNitro
RSthiol/sulfide
OHCAldehyde
ROCKetone
HO2CC-acid
RO2CC-ester
H 2NOCC-amide
NCNitrile
ortho
meta
para
0.0
0.0
0.0
-0.2
-0.1
-0.2
0.0
0.0
0.0
0.6
0.1
0.1
-0.1
-0.1
-0.1
0.1
0.0
-0.1
1.4
0.4
-0.1
-0.3
0.0
-0.2
0.0
0.0
-0.1
0.2
-0.1
0.0
0.4
-0.2
0.9
-0.6
-0.1
-0.5
-0.5
-0.1
-0.4
-0.3
0.0
-0.1
-0.8
-0.2
-0.7
0.1
-0.1
-0.3
1.0
0.3
0.4
-0.1
-0.1
-0.2
0.6
0.2
0.3
0.6
0.1
0.2
0.9
0.2
0.3
0.7
0.1
0.2
0.6
0.1
0.2
0.4
0.2
0.3
Substitution relative to calculated "H"

meta
ortho
para
H
meta
ortho
(ppm) = 7.3 + ortho + meta + para
Example Calculation
2
H
1
CH3O
2H
H
3
CH2
4
5
H 6
H
7
1. (CH3) = 0.9 + 2.8 = 3.7

actual = 3.8
2. (2) = 7.3 + (-0.5) ortho + (-0.1) para = 6.7
actual = 6.8
3. (3) = 7.3 + (-0.2) ortho + (-0.4) para = 6.7
actual = 7.1
4. (CH 2) = 1.2 + (0.8) + (1.4) = 3.4
actual = 3.3
5. (5) = 5.2 + (0.7) gem = 5.9
actual = 5.9
6. (6) = 5.2 + (-0.2) trans = 5.0
actual = 5.1
7. (7) = 5.2 + (-0.2) cis = 5.0
actual = 5.1

Real Examples of Combination Effects on Chemical Shifts
bond anisotropy
bond example too
0.8 shielded
(CH 2)
0.8, shielded
H
shielding cone
from bond
CH2
2.6
H
7.2
electronegativity and bond

O
O
C
10-12
H O
O
C
9.5
H
1.5
deshielded
H 3C
hydrogen
bonding
O H
H
C
O
C
15, hydrogen
bonded enol
CH3
electronegative substituent and distance from protons

O CH2CH 2CH2CH2CH 3
CH3 Cl
3.0
3.6 1.5 1.3 1.3 0.9

multiple substituents
CH4
0.2
CH3CH 2 Cl
CH3CH2CH 2 Cl
1.3
1.0
CH 3Cl
CH2Cl2
3.0
= 2.8
H 3C C
CH3CH 2Cl (CH 3)2CHCl
3.0
3.5
4.1
2.4
C H 1.9
C C H 3.0
R C
Ar
RO
ArO
RS
ArO
H
H
H
H
CCl4
6.4
C
H
5.8
Ph
3.7
H 2C
H 3C
1.3
? (oops)
H 3CH2C C
Ph (H3C)2CH C
H
C
4.2
C
H
4.0
8.2
H
7.5
H
Ph
3.5
H
6.5
O
H 2N
=?
3.0
H
H
H
H
H
H
bond anisotropy
produces deshielding Extra electron density via resonance produces
shielding effect on aromatic protons, especially
effect on aromatic
at ortho/para positions.
protons.
sp C-H
H C C H
CHCl3
2.6
alkene substituent resonance and inductive effects

0.9 1.4 2.0
O
3.8
H
H CH CH CH
H 5.0 CH O C
3
2
2
3
C C
C C
C
H
H
H
H
H
5.8
4.9
5.3
6.1
aromatic resonance and inductive effects
6.6
H
H 7.3
7.1
H
H
6.7
H
H
H 2N
H
0.9
substituents at methyl (CH3), methylene (CH2) and methine (CH)

CH3Cl
0.9
7.2
= 1.9
5.3
= 2.3
CH3CH 2CH 2CH2 Cl CH3CH 2 R
7.7
H
C O
H 3C
2.1
H
C
H
7.3
4.9
C
H
4.6
O
N
O
H
H
H
H
Withdrawal of electron density via resonance
produces deshielding effect on aromatic protons,
especially at ortho/para positions.
O
R2N H amine H = 1-5 enol H = 10-17 H O

alcohol H = 1-5
C C
phenol H = 4-10
O
O
amide H = 5-8
thiol H = 1-2.5
R C
R C
aromatic thiol H = 3-4
NH2
O H acid H = 10-13
10
1. One nearest neighbor proton

H1
observed
proton
Ha
increasing
one neighbor
proton = Ha
increasing E (, Bo)
the ratio of these

two populations
is about 50/50 (or 1:1)
H1
perturbation(s) by
neighbor proton(s)
Eto flip proton
E2 (observed)
E1 (observed)
Bo
J1a
1
Protons in this environment have a small cancellation

of the external magnetic field, Bo, and produce a
smaller energy transition by that tiny amount.
H1
C
H1
C
J = coupling constant
small difference in
energy due to differing
neighbor's spin (in Hz)
Protons in this environment have a small

additional increment added to the external
magnetic field, Bo, and produce a higher
energy transition by that tiny amount.
N + 1 rule (N = # neighbors)
J (Hz)
# peaks = N + 1 = 1 + 1 = 2 peaks
(ppm)
2. Two nearest neighbor protons (both on same carbon or one each on separate carbons)
observed
proton
H1
two neighbor
Ha protons
the ratio of these

four populations
is about 1:2:1
Hb
H1
E1
Eto flip proton
E2
J1a
E3
Bo
H1
C
two neighbor protons are like

two small magnets that can be
arranged four possible ways
(similar to flipping a coin twice)
J1b
two equal energy

populations here
J1b
J (Hz)
J (Hz)
# peaks = N + 1 = 2 + 1 = 3 peaks
(ppm)
3. Three nearest neighbor protons (on same carbon, or two on one and one on another, or one each on separate carbons)
H1
observed
proton
three neighbor
Ha protons
C C
the ratio of these

eight populations
is about 1:3:3:1
Hb
H1
Hc
Eto flip proton
E1
E2
Bo
H1
C C
E3
J1a
E4
J1b
three neighbor protons are like

three small magnets that can be
arranged eight possible ways
(similar to flipping a coin thrice)
three equal energy

populations at each
of middle transitions
J1c
J1b
J1c
J1c
J (Hz)
J (Hz)
(ppm)
J (Hz)
# peaks = N + 1 = 3 + 1 = 4 peaks
11
Splitting patterns when the N+1 rule works (common, but not always true)
= group without any coupled proton(s)
N=1
N=0
N=2
H
H
C
N=3
H
H
C
H2
C
CH
CH2
CH3
CH
CH
CH
= calc or exp
CH
d, J=7
I=1H
N=1
t, J=7
I=1H
N=2
= calc or exp
= calc or exp
s, J=none
I=1H
N=0
CH
q, J=7
I=1H
N=3
= calc or exp
N=4
N=5
H
C
H
CH
CH3
CH2
CH
CH2
CH3
CH3
CH
CH
CH
CH2
CH2
CH2
CH2
CH
sex, J=7
I=1H
N=5
qnt, J=7
I=1H
N=4
= calc or exp
= calc or exp
N=6
N=7
H
H
C
CH
CH3
CH3
H2C
CH2
CH
CH2
H2 C
CH3
H
CH3
CH3
sep, J=7
I=1H
N=6
oct, J=7
I=1H
N=7
CH3
CH2
= calc or exp
= calc or exp
N=8
H2 C
Pascal's triangle = coefficients of variable terms in binomial expansion (x + y)n, n = integer
Multiplets when the N + 1 rule works (all J values are equal).

H2C
CH3
CH3
non, J=7
I=1H
N=8
1 peak = 100%
s = singlet
d = doublet
t = triplet
1
1
1
q = quartet
qnt = quintet
sex = sextet
= calc or exp
sep = septet
o = octet
1
1
1
1
6
7
2
3
4
5
1 peak = 50%
1 peak = 25%
1
1
3
6
1 peak = 12%
1
10 10 5
1 peak = 6%
1
1 peak = 3%
1
15 20 15 6
1
21 35 35 21 7 1
relative sizes of
peaks in multiplets
(% edge peak shown)
1 peak = 1.5%
1 peak = 0.8%
Combinations or these are possible.

dd = doublet of doublets; ddd = doublet of doublet of doublets; dddd = doublet of doublet of doublet of doublets; dt = doublet of triplets
td = triplet of doublets; etc.
12
Typical Coupling Constants

Ha
Range
Typical
0-30 Hz
14 Hz
Hb
geminal protons - can have different chemical shifts
and split one another if they are diastereotopic
Range
Typical
6-8 Hz
= dihedral
angle
Range
0-3 Hz
1 Hz
Range
Typical
0-3 Hz
1 Hz
Hb
C C
Hb
trans / allylic coupling,

notice through 4 bonds
Typical
C
7 Hz
Ha
Hb
cis / allylic coupling,

vicinal protons are on adjacent atoms, when freely

rotating coupling averages out to about 7 Hz
Ha Hb
C
C
Typical
Ha
Ha Hb
C
Ha
Range
0-12 Hz
7 Hz
depends on dihedral
angle, see plot of
Karplus equation
Range
Typical
0-1 Hz
0 Hz
Range
Typical
9-13 Hz
10 Hz
Range
Typical
1-3 Hz
2 Hz
Range
Typical
5-8 Hz
6 Hz
Range
Typical
2-3 Hz
2 Hz
Range
Typical
2-3 Hz
3 Hz
C
C
Hb
Ha
sp2 vicinal coupling

(different bonds)
Ha
C
Hb
C
O
sp3 vicinal aldehyde coupling
protons rarely couple through 4 chemical bonds

unless in a special, rigid shapes (i.e. W coupling)
Ha
C
Range
Typical
0-3 Hz
2 Hz
Hb
Hb
C
Range
Typical
5-11 Hz
10 Hz
C
Hb
Range
Typical
11-19 Hz
17 Hz
sp2 trans coupling (always

larger than the cis isomer)
C
C
Hb
C C
Hb
Hb
Ha
C
C C
bis-propargylic coupling
Range
Ha
C
Ha
sp / propargylic coupling
sp2 cis (acylic) coupling (always

smaller than the trans isomer)
sp vicinal aldehyde coupling
Ha
sp2 geminal coupling
Ha
Hb
Ha
4-10 Hz
Typical ortho, meta and

para coupling to
7 Hz this proton
Range
H ortho
H meta
sp2 / sp3 vicinal coupling
ortho 6-10 Hz
meta 2-3 Hz
para 0-1 Hz
Hpara
When J values are less than 1 Hz, it is often difficult to resolve them and a peak may merely appear wider and shorter.
Typical
9 Hz
2 Hz
0 Hz
13
Similar chemical shift information presented in a different format. Remember, proton decoupled
carbons appear as singlets. When carbons are coupled to their hydrogens, carbons follow the N+1 rule.
Methyls = q, methylenes = t, methines = d, and carbons without hydrogen appear as singlets = s.
DEPT provides the same information. Carbon chemical shifts are spread out over a larger
range than proton chemical shifts (they are more dispersed), so it is less likely that two different carbon
shifts will fall on top of one another. The relative positions of various types of proton and
carbon shifts have many parallel trends (shielded protons tend to be on shielded carbons, etc.)
CH2
CH3
Simple alkane
carbons
0 - 30 ppm
(q)
20 - 40 ppm
(t)
50 - 60 ppm
CH2 N
d
10 - 50 ppm
(t)
CH2 X
sp3 carbon next to

bromine or chlorine
(X = Cl, Br)
sp carbon (alkynes)
sp2 carbon (alkenes

and aromatics)
25 - 50 ppm
(t)
60 - 80 ppm d
(d)
50 - 70 ppm d
(d)
60 - 80 ppm
(d)
50 - 70 ppm
(s)
C
70 - 90 ppm
70 - 90 ppm
(s)
C N
sp carbon (nitriles)
60 - 80 ppm
(s)
C N
110 - 125 ppm
C
180 - 210 ppm
aldehyde carbons, lower

values when conjugated
(d)
O
C
140 - 160+ ppm

sp carbon attached to an electronegative atom
(X = oxygen, nitrogen, halogen) or C carbon
conjugated with a carbonyl group
100 - 140 ppm
simple sp2 carbon

resonance donation moves lower,
resonance withdrawal moves higher
160 - 180 ppm

carboxyl carbons
(acids, esters, amides)
(s)
C O
CH X
30 - 60 ppm
(s)
CH N
35 - 55 ppm
(q)
(t)
CH3 N
30 - 50 ppm
(d)
CH O
55 - 80 ppm
(q)
sp3 carbon
next to nitrogen
CH2 O
CH3 O
sp3 carbon
next to oxygen
CH
R
180 - 220 ppm
ketone carbons, lower

values when conjugated
(s)
14
Calculations of alkane 13C chemical shifts not listed above.

sp3 Carbon Chemical Shift Calculations
Calculations for sp3 carbon 13C chemical shifts of functionalized carbon skeletons can be performed starting
from the actual shifts found in the corresponding alkane skeleton, and introducing corrections factors based on the
functionality present in the molecule. This assumes that the alkane 13C shifts are available, which is why several
examples are provided below.
Examples of Cn alkanes as possible starting points for calculation 13C shifts in ppm.
Approximate 13C shift calculation from scratch.
Steric Corrections for sp3 carbon chemical shift calculations

The attached C carbons are:
C = -(2) + 9x(# + #) - 2x(# ) + steric corrections
The calculated
carbon atom is:
primary
quaternary
tertiary
primary
-1.1
-3.4
secondary
-2.5
-7.5
-15.0
tertiary
quaternary
13
secondary
-3.7
-9.5
-1.5
-8.4
-15.0
C1 = -2 + 9(1+3) - 2(2) + (-3) = 29
(actual = 28.3)
C2 = -2 + 9(4+2) - 2(2) + [3x(-1.5)+(-15.0)] = 28

2
C3 = -2 + 9(3+5) - 0(2) + [(-9.5)+(-15.0)] = 45
-25.0
(actual = 34.0)
(actual = 47.9)
C4 = -2 + 9(3+2) - 3(2) + (-9.5) = 27

C5 = -2 + 9(1+2) - 2(2) + (-1) = 20
(actual = 27.2)
(actual = 19.5)
C6 = -2 + 9(1+2) - 5(2) + (-1) = 14
(actual = 8.5)
C shifts for various carbon alkane skeletons - useful starting points for calculating sp3 carbon chemical shifts
C3
C2
CH4
-2.3
15.8
5.9
C6
22.9
14.1
28.1
48.9
29.3
18.8
39.0
33.9
29.8
29.7
34.4
39.2
35.3
14.5
25.2
C9
14.1
39.2
C10
22.8
29.6
32.1
29.8
26.9
42.3
14.2
29.6
22.8
27.2
28.1
40.6
38.0
22.7
32.1
12.0
31.8
17.9
37.2
C8
14.1
18.1
17.5
27.0
36.4
29.5
15.0
14.7
48.3
33.4
11.0
9.1
22.9
32.0
31.9
20.3
27.0
25.6
29.7
19.5
14.1
23.1
32.0
11.8
36.5
11.4
29.9
32.1
34.4
8.9
30.4
19.2
22.7
29.3
22.9
36.3
14.4
30.2
29.0
11.5
41.5
22.6
14.1
20.6
32.9
C7
25.0
13.8
27.9
22.3
C5
25.4
25.0
22.7
22.9
14.1
C4
16.3
32.3
14.1
22.9
29.6
32.2
11.5
34.6
14.5
36.5
19.3
29.7
14.1
20.3
39.6
32.4
19.7
29.9
10.9
40.3
25.6
35.4
20.1
14.6

X
C correction C correction
C correction
X is attached to a terminal carbon atom (ppm)

Substituent = X
15
X is attached to an internal carbon atom (ppm)

C correction
CH3
-2
-2
CH2CH3
18
-2
-2
CH(CH3)2
26
-2
14
-2
C(CH3)3
32
-2
20
-2
C
H
CH2
20
-1
15
-1
CH
-4
-4
23
-2
17
-2

Substituent = X
C correction

C correction
OH
48
10
-6
44
-4
OR
60
-6
57
-6
51
-6
49
-6
NH2
28
10
-5
24
-5
NH(CH3)
38
-5
32
-4
N(CH3)2
45
-5
37
-4
-5
21
-5
-5
-5
O
O
C
R
O
H
N
26
C
R
NO2
62
58
16

Substituent = X
C correction

C correction
70
-7
67
-7
Cl
31
10
-5
36
-5
Br
20
10
-4
28
10
-4
-7
11
-2
11
-2
30
-3
24
-1
-3
31
-3
26
-3
22
-3
18
-3
O
C
H
O
C
CH3
O
C
OH

Substituent = X
C correction

C correction
20
-3
16
-3
25
-3
19
-3
-3
-3
33
-3
30
-3
SH
11
10
-3
12
-3
SR
22
-3
20
-3
C
OCH3
O
C
NH2
C
N
O
C
Cl
17
Additional starting point for calculating 13C chemical shifts (ppm) of substituted benzene rings (just a few possibilities)
Substituent
128 ppm starting point for
benzene carbon
Use correction term for carbon

atom in relative position to the
substituent. Start with 128 ppm.
Starting points for other common ring

systems. (ppm). No correction terms
included for substituents.
3
Z1
0
9
12
10
11
20
19
8
9
9
11
12
15
2
2
12
7
6
6
13
-6
8
34
5
-5
-31
Substituent
-H
-CH3
-CH2CH3
-CH2CH2CH3
-CH2CH2CH2CH3
-CH(CH3)2
-C(CH3)3
-CH2F
-CH2Cl
-CH2Br
-CH2I
-CH2OH
-CH2NH2
-CH2NO2
-CH2CN
-CH2SH
-CH2CHO
-CH2COCH3
-CH2CO2H
-CH2=CH2
-CCH
-C6H5
-F
-Cl
-Br
-I
Z2
0
1
-1
0
0
-2
-3
-1
0
1
-1
-1
-1
2
0
-1
1
1
1
-3
4
-1
-13
0
3
9
Z3
0
0
0
0
0
0
0
0
0
0
0
0
0
1
-1
0
0
0
0
0
0
0
2
1
2
2
Z4
0
-3
-3
-3
-3
-3
-3
0
0
0
-1
-1
-2
1
-1
-2
-1
-2
-1
-1
0
-1
-4
2
-1
-1
Z1
29
34
28
18
10
22
23
22
37
20
4
10
18
12
16
-16
8
9
2
2
5
11
-43
-36
Substituent
-OH
-OCH3
-OC6H5
-NH2
-NHCOCH3
-NHOH
-NHNH2
-N=N-R
-NO
-NO2
-SH
-SCH3
-S(O)CH3
-SO2CH3
-SO2Cl
-CN
-CHO
-COCH3
-CO2H
-CO2CH3
-CONH2
-COCl
-Li
-MgBr
Z2
-13
-14
-11
-13
-8
-13
-16
-6
-8
-5
1
-2
-5
-1
-2
3
1
0
2
1
-1
0
-13
-11
Z3
1
1
0
1
0
-2
1
0
1
1
0
0
1
1
1
1
0
0
0
0
0
0
2
3
126
128
Z4
-7
-8
-7
-10
-4
-5
-10
-3
7
6
-3
-4
2
5
7
4
6
4
5
4
3
-3
3
4
134
naphathalene
136
124
pyridine
150
108
pyrrole
N
H
118
110
furan
143
126
thiophene
125
Additional starting point for calculating 13C chemical shifts (ppm) of substituted alkenes (just a few possibilities)
123 ppm starting point for alkene carbon
'
C
'
C
Z
C
2
'
C
C = 123 ppm + Zi
123 + correction factors

increments for directly attached carbon atoms
' = -8
= 11
' = -2
=5
'= 2
= -2
steric corrections
for each pair of cis-, ' substituents
for each pair of geminal-, substituents
for each pair of geminal-, 'substituents
if one or more sutstituents are present
C
1
-1
-5
3
2
Effect of substituents on alkene 13C shifts (ppm)

Substituent
-H
-CH3
-CH2CH3
-CH2CH2CH3
-CH(CH3)2
-C(CH3)3
-CH2Cl
-CH2Br
-CH2I
-CH2OH
-CH=CH2
-CCH
-C6H5
Z1
0
13
17
16
23
26
10
11
14
14
14
-6
12
Z2
0
-7
-10
-9
-12
-15
-6
-5
-4
-8
-7
6
-11
Substituent
-F
-Cl
-Br
-I
-OCH3
-O2CCH3
-N(CH3 )2
-NO2
-CN
-SCH2CH3
-CHO
-COCH3
-CO2H
-COCl
Z1
24
3
-9
-38
29
18
28
22
-15
9
15
14
5
8
Z2
-34
-6
-1
7
-39
-27
-32
-1
14
-13
14
5
10
14
18
Common fragmentation patterns in mass spectroscopy
1. Branch next to a bond

R
C
radical cation
Pi electrons partially fill in loss of electrons at

carbocation site via resonance. This is common
fragmentation for alkenes and aromatics
bond of an alkene
or an aromatic
Characteristic carboncation stability also applies.

3o R
>
2o R
> 1o R
>
CH3
2. Branch next to an atom with a lone pair of electrons

R
X C
X C
X C
radical cation
X lone pair electrons partially fill in loss of electrons at carbocation site via resonance. This
is a common fragmentation for any atom that has a lone pair of electrons (oxygen = alcohol,
ether, ester; nitrogen = amine, amide, sulfur = thiol or sulfide, etc.). Alcohols often lose water
(M-18) and primary amines can lose ammonia (M-17).
3. Branch next to a carbonyl (C=O) bondand possible subsequent loss of carbon monoxide, CO
R1
O
R1
C O
R1
R1
C O
loss of
R2
R2
radical cation
R1 or R2 can be lost from
aldehydes, ketones, acids,
esters, amides...etc.
R2
C O
C O
An oxygen lone pair partially fill in the loss of electrons at the

carbocation site via resonance. This is a common fragmentation
pattern for any carbonyl compound and can occur from either
side, though some are more common than others.
R2
subsequent loss of CO is possible
after fragmentation so not only can
you see loss of an branch you can
see the mass of an branch.
4. McLafferty Rearrangement
O
R1
H
C
C
C
O
R1
H
C
C
C
Positive charge can be on

either fragment, which
typically have an even mass.
= alpha position
= beta position
= gama position
lost neutral
still a radical
fragment
cation
This is another common fragmentation pattern for carbonyl compounds (and other pi systems as well: alkenes, aromatics,
alkynes, nitriles, etc.). If the pi bond has at least 3 additional nonhydrogen atoms attached and a hydrogen on the "gama"
atom, the branch can curve around to a comfortable 6 atom arrangement and the pi bond can pick up a hydrogen atom and
cut off a fragment between the C and C positions. The positive charge can be seen on either fragment and usually the
fragments have an even mass (unless there is an odd number of nitrogen atoms).
radical cation
Knowing these few fragmentation patterns will allow you to make many useful predictions and
interpretations. Loss of small molecules, via elimination is common: H2O = 18, H2S = 34, CH3OH = 32,
C2H5OH = 46, NH3 = 17, CH3CO2H = 62, HF = 20, HCl = 36/38, HBr = 80/82, etc.
19
A sampling of unusual and/or miscellaneous peaks that are commonly seen, (even when they don't make sense).
R
CH3 = 15
CH3CH2 = 29
C3H7 = 43
C4H9 = 57
C5H11 = 71
C6H13 = 85
mass = 39 (R = H)
53 (R = CH3)
67 (R= CH2CH3)
also works for
R
CH2
C
H
mass = 41 (R = H)
55 (R = CH3)
69 (R= CH2CH3)
H2N
mass = 65 (R = H)
79 (R = CH3)
93 (R= CH2CH3)
mass = 27
mass = 77
RO
mass = 91 (R = H)
105 (R = CH3)
119 (R= CH2CH3)
C
H2
mass = 29 (R = H)
43 (R = CH3)
mass = 42 (R = H)
57 (R= CH2CH3)
56 (R = CH3)
71 (R = C3H7)
70 (R= CH2CH3)
105 (R = C6H5)
mass = 44
H
mass = 45 (R = H)
59 (R = CH3)
73 (R= CH2CH3)
Loss of small molecules via elimination reactions.
H2 O
mass = 18
CH3OH
32
H2 S
34
C2H5OH
46
HF HCl HBr
80
20 36 82
38
NH3 CH3CO2H
62
17
McLafferty Possibilities
H
H
O
O
R2
HC
R1
CH2
C
H2
R2
R1
R
McLafferty
Notice!
even masses
mass = 44 (R = H)
58 (R = CH3)
72 (R= CH2CH3)
86 (R = C3H7)
CH2
variable mass,
(can sometimes see
cation on this side too)
mass = 28 (R = H)
42 (R = CH3)
56 (R= CH2CH3)
70 (R = C3H7)
Similar Patterns
H
CH2
R2
R1
H
R2
H
H
R1
mass = 42 (R = H)
56 (R = CH3)
70 (R= CH2CH3)
84 (R = C3H7)
R1
mass = 92 (R = H)
106 (R = CH3)
120 (R= CH2CH3)
134 (R = C3H7)
R2
R1
C
H2
H
C
R2
R1
CH2
C
H2
R2
R
R2
R1
C
H2
H
H2C
R1
C
H2
R2
C
CH2
mass = 40 (R = H)
54 (R = CH3)
68 (R= CH2CH3)
82 (R = C3H7)
R2
R1
CH2
mass = 41 (R = H)
55 (R = CH3)
69 (R= CH2CH3)
83 (R = C3H7)

Table For FTIR

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Table For FTIR

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Spectroscopy Data Tables

Infrared Tables (short summary of common absorption frequencies)

sp2 C-X single bonds

not very useful

Bonds to Hydrogen (stretching wave numbers)

amides = strong, amines = weak

Z:\files\classes\spectroscopy\typical spectra charts.DOC

sp C-X triple bonds

Spectroscopy Data Tables

Carbonyl Highlights (stretching wave numbers)

saturated = 1760, 1820

sp2 C-H bend patterns for alkenes

sp2 C-H bend patterns for aromatics

Z:\files\classes\spectroscopy\typical spectra charts.DOC

Aromatic compounds have characteristic weak overtone bands

Spectroscopy Data Tables

1500 1400 1300 1200 1100 1000 900 800 700

aromatic sp2 C-H

1500 1400 1300 1200 1100 1000 900

carboxylic acid O-H

alkene sp2 C-H

alkene sp2 C-H

aromatic sp2 C-H

Saturated C=O lies at

expansion of carbonyl (C=O) stretch region (units = cm-1)

carboxylic acid C=O (also acid "OH")

acid chloride C=O (high C=O, 1 peak)

anhydride C=O (high C=O, 2 peaks)

Z:\files\classes\spectroscopy\typical spectra charts.DOC

amide C=O (low C=O, amide N-H)

Spectroscopy Data Tables

IR Flowchart to determine functional groups in a compound (all values in cm-1).

has C=O band

does not have

1150-1350 (acyl, strong)

(1000-1150, alkoxy, medium)

1210-1320 (acyl, strong)

2400-3400, very broad

All IR values are approximate and have a range

1460 & 1380

sp3 C-H bend

sp2 C-H bend

sp2 C-H bend

1600 & 1480

Alkene sp C-H bending patterns

3350 & 3180, two bands

N-H bend, 1550-1640,

Inductive pull of Cl increases the

1760 & 1820 (saturated)

monosubstituted alkene (985-1000, 900-920)

Aromatic sp2 C-H bending patterns

N-H bend, 1550-1640,

1500-1600, asymmetric (strong)

There are also weak overtone bands between

3300 - 3500, two bands

1150-1350 (acyl, strong)

Z:\files\classes\spectroscopy\typical spectra charts.DOC

Spectroscopy Data Tables

deshielding side = less electron rich

shielding side = more electron rich

typical proton chemical shifts

Carbon and/or heteroatoms without hydrogen do

with & without H