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Bordwell

Values of the slope, a, of a plot of AG vs. AG obviously must lie in the range of 0-1 if the interpretation of a as the fractional resemblance of the transition state to the product is to be valid. Some examples of a values lying outside this range have been observed. - Thus, Bordwell et al. found a = 1.31 for this reaction ... [Pg.229]

We consider first the Sn2 type of process. (In some important Sn2 reactions the solvent may function as the nucleophile. We will treat solvent nucleophilicity as a separate topic in Chapter 8.) Basicity toward the proton, that is, the pKa of the conjugate acid of the nucleophile, has been found to be less successful as a model property for reactions at saturated carbon than for nucleophilic acyl transfers, although basicity must have some relationship to nucleophilicity. Bordwell et al. have demonstrated very satisfactory Brjinsted-type plots for nucleophilic displacements at saturated carbon when the basicities and reactivities are measured in polar aprotic solvents like dimethylsulfoxide. The problem of establishing such simple correlations in hydroxylic solvents lies in the varying solvation stabilization within a reaction series in H-bond donor solvents. [Pg.358]


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See also in sourсe #XX -- [ Pg.358 , Pg.413 ]

See also in sourсe #XX -- [ Pg.141 ]

See also in sourсe #XX -- [ Pg.143 ]




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Mechanism Bordwell

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