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Organic compounds characteristic proton chemical shifts

Tables 5.2 and 5.3 give characteristic shifts for nuclei in some representative organic compounds. Table 5.4 gives characteristic chemical shifts for protons in common alkyl derivatives. Table 5.5 gives characteristic chemical shifts for the olefinic protons in common substituted alkenes. To a first approximation, the shifts induced by substituents attached an alkene are additive. So, for example, an olefinic proton which is trans to a -CN group and has a geminal alkyl group will have a chemical shift of approximately 6.25 ppm [5.25 + 0.55(tra .s-CN) + 0.45(gew-alkyl)]. Tables 5.2 and 5.3 give characteristic shifts for nuclei in some representative organic compounds. Table 5.4 gives characteristic chemical shifts for protons in common alkyl derivatives. Table 5.5 gives characteristic chemical shifts for the olefinic protons in common substituted alkenes. To a first approximation, the shifts induced by substituents attached an alkene are additive. So, for example, an olefinic proton which is trans to a -CN group and has a geminal alkyl group will have a chemical shift of approximately 6.25 ppm [5.25 + 0.55(tra .s-CN) + 0.45(gew-alkyl)].

See other pages where Organic compounds characteristic proton chemical shifts is mentioned: [Pg.202]    [Pg.1291]    [Pg.512]    [Pg.152]    [Pg.456]    [Pg.394]    [Pg.916]    [Pg.165]    [Pg.262]   


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