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The ∆G° can be written as a function of change in enthalpy (∆H°) and change in entropy (∆S°) as ∆G°= ∆H° – T∆S°. Practically, enthalpies, not free energy, are used to determine whether a reaction is favorable or unfavorable, because ∆ H ° is easier to measure and T ∆ S ° is usually too small to be of any significance ...
An endergonic reaction (such as photosynthesis) is a reaction that requires energy to be driven. Endergonic means "absorbing energy in the form of work." The activation energy for the reaction is typically larger than the overall energy of the exergonic reaction (1). Endergonic reactions are nonspontaneous.
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 −1 and t 1/2 ~ 2 h. Thus, a free energy of activation of this magnitude corresponds to a typical reaction that proceeds to completion overnight at room ...
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˚ = − ...
The reaction quotient (Q r) is the ratio of the chemical activity (a i) of the reduced form (the reductant, a Red) to the activity of the oxidized form (the oxidant, a ox). It is equal to the ratio of their concentrations (C i) only if the system is sufficiently diluted and the activity coefficients (γ i) are close to unity (a i = γ i C i):
An exergonic process is one which there is a positive flow of energy from the system to the surroundings. This is in contrast with an endergonic process. [1] Constant pressure, constant temperature reactions are exergonic if and only if the Gibbs free energy change is negative (∆G < 0).
Degenerate states are also obtained when the sum of squares of quantum numbers corresponding to different energy levels are the same. For example, the three states (n x = 7, n y = 1), (n x = 1, n y = 7) and (n x = n y = 5) all have = and constitute a degenerate set.
In electrochemistry, the Nernst equation is a chemical thermodynamical relationship that permits the calculation of the reduction potential of a reaction (half-cell or full cell reaction) from the standard electrode potential, absolute temperature, the number of electrons involved in the redox reaction, and activities (often approximated by concentrations) of the chemical species undergoing ...