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Hammett equation nonlinear

Not all reactions can be fitted by the Hammett equations or the multiparameter variants. There can be several reasons for this. The most common is that the mechanism of the reaction depends on the nature of the substituent. In a multistep reaction, for example, one step may be rate-determining in the case of electron-withdrawing substituents, but a different step may become rate-limiting when the substituent is electron-releasing. The rate of semicarbazone formation of benzaldehydes, for example, shows a nonlinear Hammett... [Pg.213]

In 1962, Hansen [14] derived a first Hammett-type relationship between the toxicities of substituted benzoic acids and the electronic a constants of their substituents. However, later, it turned out that this was a chance correlation that only resulted from a close interrelationship between the Hammett a parameter and the lipophilicity constant % (Sec. 4 Eqs. (42) and (43)). In the same year, for the very first time, a nonlinear multiparameter equation (Eq. 6) [15] was used to describe biological activity values ... [Pg.540]


See other pages where Hammett equation nonlinear is mentioned: [Pg.375]    [Pg.402]    [Pg.676]    [Pg.344]    [Pg.147]    [Pg.207]    [Pg.189]    [Pg.402]    [Pg.541]    [Pg.5]   
See also in sourсe #XX -- [ Pg.213 ]

See also in sourсe #XX -- [ Pg.213 ]




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