spectrum, and therefore aqueous solutions may readily be studied. Overtones
and combination vibrations occur less often. Vibrations of symmetrical struc-
tures, such as R-C∫C-R, which are weak in the IR, appear as strong bands in
the R.E10 – Infrared and Raman spectrometry: principles and instrumentation 237
Table 1. H–X group frequencies
X Wavenumber (cm-^1 ) Comment
H-C (aliphatic) 2960–2900 Strong
H-C (aromatic) 3050 - 3000 Strong
H-C (alkyne) 3300
H-O 3600 Free OH
H-O 3500 - 2500 H-bondedH-N 3500–3300 Broad
H-S 2600 - 2500 WeakTable 2. Multiple bonds
Bond Wavenumber (cm-^1 ) Comment
Single C-C Approx. 1200 Variable
Aromatic C:::C 1600, 1500
Double C=C 1650
Triple C∫C 2200 Weak
Single -C-N 1100 Variable
Double -C=N- 1670
Triple -C∫N 2250 StrongS t r e t c h i n g B e n d i n gHydrocarbons
and
C–H groupsOxygen
compoundsHeteroatom
compounds4000 3000 2000 1500
Wavenumber (cm–1)1000 500m–s
m–C–H(sat) m C–C*
=C–Hs =C–H v C=Cv C–Ov C=Cv Ar–Hv O–H
w H–CO s C=Om N–H v C–N*
m–s C=N s N=O s C–CI
m–s C–Hm–s Ar–Hm–s N–Hm =C–Hs O–Hw
Chain rockv Ar ringFree H-bondedFig. 3. Chart of characteristic infrared group frequencies. *Not so useful for characterization.