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For a given set of reaction conditions, the equilibrium constant is independent of the initial analytical concentrations of the reactant and product species in the mixture. Thus, given the initial composition of a system, known equilibrium constant values can be used to determine the composition of the system at equilibrium.
For a reversible reaction, the equilibrium constant can be measured at a variety of temperatures. This data can be plotted on a graph with ln K eq on the y-axis and 1 / T on the x axis. The data should have a linear relationship, the equation for which can be found by fitting the data using the linear form of the Van 't Hoff equation
log 10 β values between about 2 and 11 can be measured directly by potentiometric titration using a glass electrode. This enormous range of stability constant values (ca. 100 to 10 11) is possible because of the logarithmic response of the electrode. The limitations arise because the Nernst equation breaks down at very low or very high pH.
Rates of reaction can be studied by examining activated complexes near the saddle point of a potential energy surface. The details of how these complexes are formed are not important. The saddle point itself is called the transition state. The activated complexes are in a special equilibrium (quasi-equilibrium) with the reactant molecules.
In a chemical reaction, chemical equilibrium is the state in which both the reactants and products are present in concentrations which have no further tendency to change with time, so that there is no observable change in the properties of the system. [1]
The reaction proceeds in the forward direction (towards larger values of Q r) when Δ r G < 0 or in the reverse direction (towards smaller values of Q r) when Δ r G > 0. Eventually, as the reaction mixture reaches chemical equilibrium, the activities of the components (and thus the reaction quotient) approach constant values.
If the mechanism for the reaction of an aromatic compound is thought to occur through one of two mechanisms, the compound can be modified with substituents with different σ values and kinetic measurements taken. Once these measurements have been made, a Hammett plot can be constructed to determine the value of ρ. If one of these mechanisms ...
However, the extent of reaction can be used to describe the changes on a common footing as needed. The change of the number of moles of A can be represented by the equation d n A = − d ξ {\displaystyle dn_{A}=-d\xi } , the change of B is d n B = + 2 d ξ {\displaystyle dn_{B}=+2d\xi } , and the change of C is d n C = + 3 d ξ {\displaystyle ...