Equilibrium Constant: Why is k Defined?

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SUMMARY

The equilibrium constant, denoted as K, is defined based on the relationship between the chemical potentials of reactants and products at equilibrium. Specifically, for the reaction A <--> B, K is expressed as (p_B/p_A)_{equil}, derived from the Gibbs Free Energy change equation, ΔG(reac) = ΔG^0(reac) - RT ln(p_B/p_A). This definition ensures that the equilibrium constant reflects the balance of forward and reverse reactions, aligning with Le Chatelier's principle. The formulation can be generalized for solutions and multi-component systems.

PREREQUISITES
  • Understanding of Gibbs Free Energy and its relation to chemical reactions
  • Familiarity with chemical potential and its mathematical representation
  • Knowledge of Le Chatelier's principle and its implications in chemical equilibrium
  • Basic concepts of ideal gas behavior in chemical reactions
NEXT STEPS
  • Study the derivation of Gibbs Free Energy in detail
  • Explore the implications of Le Chatelier's principle in various chemical systems
  • Learn about the behavior of ideal gases in equilibrium reactions
  • Investigate the generalization of the equilibrium constant for solutions and multi-component systems
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Chemistry students, chemical engineers, and researchers in thermodynamics who seek to deepen their understanding of chemical equilibrium and the mathematical foundations of the equilibrium constant.

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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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