Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Endergonic reaction, Hammond

Enantiotopic (NMR), 455 Endergonic. 153 Endergonic reaction, Hammond postulate and, 197-198 Endo stereochemistry, Diels-Alder reaction and, 495 Endothermic, 154 -ene, alkene name ending, 176 Energy difference, equilibrium position and, 122... [Pg.1296]

Markovnikov s rule can be restated by saying that, in the addition of HX to an aikene, the more stable carbocation intermediate is formed. This result is explained by the Hammond postulate, which says that the transition state of an exergonic reaction step structurally resembles the reactant, whereas the transition state of an endergonic reaction step structurally resembles the product. Since an aikene protonation step is endergonic, the stability of the more highly substituted carbocation is reflected in the stability of the transition state leading to its formation. [Pg.204]

Hammond postulate (Section 6.10) A postulate stating that we can get a picture of what a given transition state looks like by looking at the structure of the nearest stable species. Exergonic reactions have transition states that resemble reactant endergonic reactions have transition states that resemble product. [Pg.1243]

When AG° < A., the predictions of such an equation are in agreement with the deductions of the Hammond postulate. Indeed, for exergonic reactions, tends to zero when AG° —> — A, which corresponds to an activationless reaction. Conversely, for endergonic reactions, tends to unity when AG° —>X, which features a barrierless reaction. [Pg.32]

The Hammond and Cordes-Thornton coefficients can be utilised to characterise transition states in terms of structure reactivity surfaces as follows. The Hammond coefficient is defined so that it is positive when an increase in energy of the products (relative to reactants) accompanies an increase in the first derivative. This describes the generalisation (Hammond effect) that endergonic reactions tend to have product-like transition structures. A positive Hammond coefficient is expected for a fundamental process where structural change affects the energy of one end of a reaction coordinate, as a consequence of the maximum (negative curvature) at the saddle-point in the direction along the reaction coordinate. [Pg.110]

Using Eq. 7.64, show how Marcus theory nicely reproduces the predictions of the Hammond postulate by considering values of AG° that represen t exergonic and endergonic reactions. What kinds of reactions would you expect would not... [Pg.416]

How does the Hammond postulate apply to electrophilic addition reactions The formation of a catbocation by protonation of an alkene is an endergonic step. Thus, the transition state for alkene protonation structurally resembles the... [Pg.198]


See other pages where Endergonic reaction, Hammond is mentioned: [Pg.198]    [Pg.346]    [Pg.14]    [Pg.14]    [Pg.12]    [Pg.237]    [Pg.198]    [Pg.217]    [Pg.237]    [Pg.198]    [Pg.1054]    [Pg.217]    [Pg.243]    [Pg.246]    [Pg.253]    [Pg.236]    [Pg.283]    [Pg.247]    [Pg.170]    [Pg.14]    [Pg.26]    [Pg.35]    [Pg.12]    [Pg.218]    [Pg.238]   


SEARCH



Endergonic

Endergonic reaction

Hammond

© 2024 chempedia.info