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Cyclic ring systems carbon-13 chemical shifts

Several trends have emerged in the extensive carbon-13 NMR spectroscopy data that have been accumulated for sulfones and sulfoxides. Based on many studies of cyclic systems—particularly five- and six-membered ring sulfur compounds—these trends were shown to generally apply equally to both the cyclic and acyclic systems . Thus (a) oxidation of a sulfide to a sulfone results in a 20-25 ppm downfield chemical shift for sp -hybridized a-carbon atoms and 4-9 ppm upfield shift for / -carbons , and (b) there is very little difference between the chemical shifts of a-carbon atoms of sulfones and sulfoxides despite the difference in the inductive effects of these two functional groups . A difference is observed, however, in the H chemical shift of related cyclic sulfoxides and sulfones . [Pg.396]


See other pages where Cyclic ring systems carbon-13 chemical shifts is mentioned: [Pg.357]    [Pg.51]    [Pg.441]    [Pg.441]    [Pg.112]    [Pg.51]    [Pg.51]    [Pg.51]    [Pg.396]    [Pg.201]    [Pg.441]    [Pg.81]    [Pg.441]    [Pg.81]    [Pg.69]    [Pg.81]    [Pg.783]    [Pg.78]    [Pg.332]    [Pg.326]    [Pg.240]    [Pg.240]    [Pg.56]   
See also in sourсe #XX -- [ Pg.7 , Pg.100 ]

See also in sourсe #XX -- [ Pg.7 , Pg.100 ]




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