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In chemical thermodynamics, an endergonic reaction (from Greek ἔνδον (endon) 'within' and ἔργον (ergon) 'work'; also called a heat absorbing nonspontaneous reaction or an unfavorable reaction) is a chemical reaction in which the standard change in free energy is positive, and an additional driving force is needed to perform this ...
Using the Eyring equation, there is a straightforward relationship between ΔG ‡, first-order rate constants, and reaction half-life at a given temperature. At 298 K, a reaction with ΔG ‡ = 23 kcal/mol has a rate constant of k ≈ 8.4 × 10 −5 s −1 and a half life of t 1/2 ≈ 2.3 hours, figures that are often rounded to k ~ 10 −4 s ...
An endergonic reaction is an anabolic chemical reaction that consumes energy. [3] It is the opposite of an exergonic reaction. It has a positive ΔG because it takes more energy to break the bonds of the reactant than the energy of the products offer, i.e. the products have weaker bonds than the reactants.
Thus, is positive if the unfolded state is less stable (i.e., disfavored) relative to the native state. The most direct way to measure the conformational stability Δ G o {\displaystyle \Delta G^{o}} of a molecule with two-state folding is to measure its kinetic rate constants k f {\displaystyle k_{f}} and k u {\displaystyle k_{u}} under the ...
The main factor affecting the formal (or apparent) reduction potentials ′ in biochemical or biological processes is the pH. To determine approximate values of formal reduction potentials, neglecting in a first approach changes in activity coefficients due to ionic strength, the Nernst equation has to be applied taking care to first express ...
In theoretical chemistry, an energy profile is a theoretical representation of a chemical reaction or process as a single energetic pathway as the reactants are transformed into products. This pathway runs along the reaction coordinate , which is a parametric curve that follows the pathway of the reaction and indicates its progress; thus ...
and they have positive (endergonic) or negative (exergonic) Gibbs free energies of reaction . As Marcus calculations refer exclusively to the electrostatic properties in the solvent (outer sphere) Δ G ∘ {\displaystyle \Delta G^{\circ }} and λ 0 {\displaystyle \lambda _{0}} are independent of one another and therefore can just be added up.
Hammond's postulate (or alternatively the Hammond–Leffler postulate), is a hypothesis in physical organic chemistry which describes the geometric structure of the transition state in an organic chemical reaction. [1] First proposed by George Hammond in 1955, the postulate states that: [2]