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Carbenium ions, carbocation classification

Carbocations are central to hydrocarbon chemistry (/). Much of this chemistry is based on acid catalysis, which leads to generation of positive ions of carbon. The resulting intermediates are classified as carbenium and carbonium ions, as proposed by Olah (2-4). Carbonium ions are the penta- or higher coordinate carbocations that maintain 8 valence electrons via 2-electron/3-center bonding, quite different from carbenium ions that possess only 6 valence electrons. Figure 1 shows a systematic classification of carbocations. [Pg.310]

Figure 1. Classification of carbocations into carbonium and carbenium ions,... Figure 1. Classification of carbocations into carbonium and carbenium ions,...
The analysis of the effect that the different substituents may have on the rate coefficients in this case is particularly hard to perform by using simple inductive effects, as described for instance by the Hammett substituent constants. Note that, despite the fact that most of the 28 carbenium ions exhibit para substitution, the general structure on top of Chart 6, shows a complex substitution pattern at the carbocation centre. In order to asses the effect of multiple substitution at this site, we first considered those compounds that have two fixed hydrogen atoms at the -position of the phenyl group, which according to Hammett classification have crp(H) = 0.0, and the third phenyl group substituted at -position with H (compound 96 in Chart 6) OCH3 (compound 97 in... [Pg.173]

In 1972 Olah proposed a classification for carbocations dividing them into trivalent ( classical ) carbenium ions and penta- and tetracoordinate ( non-classical ) carbonium ions. [Pg.8]


See also in sourсe #XX -- [ Pg.298 ]

See also in sourсe #XX -- [ Pg.298 ]




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