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The constant K 2 is for a reaction with these two micro-species as products, so that [LH] = [L 1 H] + [L 2 H] appears in the numerator, and it follows that this macro-constant is equal to the sum of the two micro-constants for the component reactions. K 2 = k 21 + k 22. However, the constant K 1 is for a reaction with these two micro-species as ...
The Van 't Hoff equation relates the change in the equilibrium constant, K eq, of a chemical reaction to the change in temperature, T, given the standard enthalpy change, Δ r H ⊖, for the process. The subscript r {\displaystyle r} means "reaction" and the superscript ⊖ {\displaystyle \ominus } means "standard".
In thermodynamics, the ebullioscopic constant K b relates molality b to boiling point elevation. [1] It is the ratio of the latter to the former: = i is the van 't Hoff factor, the number of particles the solute splits into or forms when dissolved. b is the molality of the solution.
If the reaction is first order it has the unit s −1, and for that reason it is often called the frequency factor or attempt frequency of the reaction. Most simply, k is the number of collisions that result in a reaction per second, A is the number of collisions (leading to a reaction or not) per second occurring with the proper orientation to ...
where K is the stability constant for the competition reaction. Thus, the value of the stability constant K A B {\displaystyle K_{AB}} may be derived from the experimentally determined values of K and K A C {\displaystyle K_{AC}} .
This is exploited in drug development to increase the concentration of a compound in the blood by adjusting the pK a of an ionizable group. [78] Knowledge of pK a values is important for the understanding of coordination complexes, which are formed by the interaction of a metal ion, M m+, acting as a Lewis acid, with a ligand, L, acting as a ...
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Some multistep reactions can also have apparent negative activation energies. For example, the overall rate constant k for a two-step reaction A ⇌ B, B → C is given by k = k 2 K 1, where k 2 is the rate constant of the rate-limiting slow second step and K 1 is the equilibrium constant of the rapid