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Pericyclic reactions, pressure effects, high

One question that needs to be addressed is why are the activation volumes of pericyclic cycloadditions smaller (more negative) than those of the corresponding stepwise reactions involving diradical intermediates In the past it was assumed that the simultaneous formation of two new n bonds in a pericyclic [4 - - 2] cycloaddition leads to a larger contraction of volume than the formation of one bond in the stepwise process. The interpretation presented [28] is limited by the scope of Eyring transition state theory where the activation volume is related to the transition state volume, as mentioned above, and does not incorporate dynamic effects related to pressure-induced changes in viscosity [41]. An extensive discussion of reaction rates in highly viscous solvents can be found in Chapter 3. [Pg.52]


See other pages where Pericyclic reactions, pressure effects, high is mentioned: [Pg.374]    [Pg.548]    [Pg.568]    [Pg.548]    [Pg.568]    [Pg.44]    [Pg.355]    [Pg.35]    [Pg.285]    [Pg.609]    [Pg.610]   


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