Page 202 - Academic Press Encyclopedia of Physical Science and Technology 3rd Analytical Chemistry
P. 202

P1: GRB/MBQ  P2: GLM Final Pages
 Encyclopedia of Physical Science and Technology  EN007C-340  July 10, 2001  14:45







              Infrared Spectroscopy                                                                       813

                            TABLE IV Selected Spectra Structure Correlations
                                                                         )
                                   Group a            Wave number region (cm −1 b  Assignment c
                            Alkanes
                              R CH 2 R                     2936–2916 s          Out-of-phase str.
                              R CH 2 R                     2863–2843 m          In-phase str.
                              R CH 2 R                     1475–1450 m          CH 2 def.
                               CH 2 CH 2 CH 2 CH 2          726–722 w           In-phase rock d
                              R CH 3                       2972–2952 s          Out-of-phase str.
                              R CH 3                       2882–2862 m          In-phase str.
                              R CH 3                       1475–1450 m          Out-of-phase def.
                              R CH 3                       1383–1377 m          In-phase def.
                              C(CH 3 ) 2                   1389–1381 m          Sym. in-phase def.
                              C(CH 3 ) 2                   1372–1368 m          Antisym. in-phase def.
                              C(CH 3 ) 3                   1401–1393 m          Sym. in-phase def.
                              C(CH 3 ) 3                   1374–1366 s          Antisym. in-phase def.
                            Olefins
                              C C                          1680–1630 mw         C C str.
                              C CH 2                       3100–3075 w          CH 2 out-of-phase str.
                              R CH CH 2                     995–985 s           Trans CH wag e
                              R CH CH 2                     910–905 s             CH 2 wag
                              R 2 C CH 2                    895–885 s             CH 2 wag
                              RCH CHR (trans)               980–965 s           Trans CH wag
                              RCH CHR (cis)                 730–650 m           Cis CH wag
                              CH 2 CH CO OR                 970–960 m             CH 2 wag
                              CH 2 CH O R                   820–810 s             CH 2 wag
                            X Y and X Y Z
                              C C C H                      2140–2100 w          C C str.
                              C C C H                      3340–3267 s          C H str.
                              C C N                        2260–2240 m          C N str.
                               C N (conjugated)            2240–2220 v          C N str.
                              S C N                        2170–2135 m          C N str.
                              C C CH 2                     2000–1900 s          Out-of-phase str.
                               N C O                       2275–2263 s          Out-of-phase str.
                               N C S                       2150–2050 s          Out-of-phase str.
                            Aromatics
                              Aromatic CH                  3100–3000 w          CH str.
                              Aromatic ring                1620–1585 v          Ring str.
                              Aromatic ring                1590–1565 v          Ring str.
                              Aromatic ring                1525–1470 v          Ring str.
                              Mono and meta                 710–665 s           Ring bend out of plane
                              Five adjacent ring H’s        800–730 s           In-phase CH wag
                              Four adjacent ring H’s        805–735 s           In-phase CH wag
                              Three adjacent ring H’s       825–750 s           In-phase CH wag
                              Two adjacent ring H’s         860–795 s           In-phase CH wag
                              Isolated ring H               935–810 s           CH wag
                            Carbonyls
                              R CO R                       1725–1705 s          C O str.
                              Conjugated ketones           1700–1640 s          C O str.
                              R CO H                       1740–1720 s          C O str.
                              Aryl CO H                    1710–1685 s          C O str.
                              R CO O R                     1750–1735 s          C O str.
                                                                                         continues
   197   198   199   200   201   202   203   204   205   206   207