Equilibrium Constant: Why is k Defined?

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The equilibrium constant, K, is defined based on the relationship between the Gibbs free energy change and the chemical potentials of reactants and products at equilibrium. At equilibrium, the change in free energy (ΔG) is zero, leading to the expression ΔG^0(reac) = -RT ln(p_B/p_A) at equilibrium, where p_B and p_A are the partial pressures of products and reactants, respectively. This formulation highlights that K can be expressed as the ratio of these partial pressures at equilibrium. The definition is versatile and can be applied to various systems, including solutions and multi-component reactions. Additionally, this definition aligns with Le Chatelier's principle, as it maintains the balance between forward and reverse reactions, linking the equilibrium constant to the rate constants of those reactions.
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Why is the equilibrium constant, k defined the way it is?

There are other expressions that would also be constant at the chemical equilibrium. These expressions could contain terms that are concentrations of the chemicals at eqiulibrium which will always be constants. So multiply a bunch of constants and get a constant, every time.
 
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It follows from the expression for the reaction free energy. Consider, for example, the equilibrium A <--> B, where both are ideal gases. Then, the reaction free energy change, defined by
\Delta G(reac) = \left( \frac{\partial G} {\partial x} \right) _{p,T}

where x is the reaction co-ordinate, is clearly equal to difference in chemical potentials of A and B (follows directly from definition of the Gibb's Free Energy). Then, the reason for the particular form of the equilibrium constant is seen to come from the variation of the chemical potential with p,T.

\mu_ i = \mu_ i^0 + RT~ ln~p_i ~ \implies \Delta G (reac) = \mu _B - \mu _A = \Delta G^0(reac) +RT ~ln(p_B/p_A)

At equilibrium, \Delta G(reac) = 0

Plug this in above, and you have,
\Delta G^0(reac) = -RT ~ ln(p_B/p_A)_{equil}

This is the motivation to define K = (p_B/p_A)_{equil}, for this particular system. The definition can be generalized to solutions and to systems with more components.

In a more simplistic argument, one might say that the above definition provides, by means of comparing the ionic product with the equilibrium constant, a direct means of relating to le Chatelier's principle. In other words, it preserves the sanctity of forward and backward reactions, and hence, provides a simple relationship between the equilibrium constant and the forward and reverse rate constants, through the definition of equilibrium as experiencing equal forward and reverse rates.
 
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