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  2. Endergonic reaction - Wikipedia

    en.wikipedia.org/wiki/Endergonic_reaction

    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 ...

  3. Spontaneous process - Wikipedia

    en.wikipedia.org/wiki/Spontaneous_process

    In thermodynamics, a spontaneous process is a process which occurs without any external input to the system. A more technical definition is the time-evolution of a system in which it releases free energy and it moves to a lower, more thermodynamically stable energy state (closer to thermodynamic equilibrium).

  4. Gibbs free energy - Wikipedia

    en.wikipedia.org/wiki/Gibbs_free_energy

    Its symbol is Δ f G˚. All elements in their standard states (diatomic oxygen gas, graphite, etc.) have standard Gibbs free energy change of formation equal to zero, as there is no change involved. Δ f G = Δ f G˚ + RT ln Q f, where Q f is the reaction quotient. At equilibrium, Δ f G = 0, and Q f = K, so the equation becomes Δ f G˚ = − ...

  5. Transition state theory - Wikipedia

    en.wikipedia.org/wiki/Transition_state_theory

    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 ...

  6. Thermodynamic free energy - Wikipedia

    en.wikipedia.org/wiki/Thermodynamic_free_energy

    Several free energy functions may be formulated based on system criteria. Free energy functions are Legendre transforms of the internal energy. The Gibbs free energy is given by G = H − TS, where H is the enthalpy, T is the absolute temperature, and S is the entropy. H = U + pV, where U is the internal energy, p is the pressure, and V is the ...

  7. Marcus theory - Wikipedia

    en.wikipedia.org/wiki/Marcus_theory

    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.

  8. Hydration energy - Wikipedia

    en.wikipedia.org/wiki/Hydration_energy

    If the solvation energy is positive, then the solvation process is endergonic; otherwise, it is exergonic. For instance, water warms when treated with CaCl 2 (anhydrous calcium chloride) as a consequence of the large heat of hydration. However, the hexahydrate, CaCl 2 ·6H 2 O cools the water upon dissolution. The latter happens because the ...

  9. Gibbs–Helmholtz equation - Wikipedia

    en.wikipedia.org/wiki/Gibbs–Helmholtz_equation

    The definition of the Gibbs function is = + where H is the enthalpy defined by: = +. Taking differentials of each definition to find dH and dG, then using the fundamental thermodynamic relation (always true for reversible or irreversible processes): = where S is the entropy, V is volume, (minus sign due to reversibility, in which dU = 0: work other than pressure-volume may be done and is equal ...