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The equilibrium constant value can be determined if any one of these concentrations can be measured. The general procedure is that the concentration in question is measured for a series of solutions with known analytical concentrations of the reactants.
The Henderson–Hasselbalch equation relates the pH of a solution containing a mixture of the two components to the acid dissociation constant, K a of the acid, and the concentrations of the species in solution. [6] Simulated titration of an acidified solution of a weak acid (pK a = 4.7) with alkali
The equilibrium constant of a chemical reaction is the value of its reaction quotient at chemical equilibrium, a state approached by a dynamic chemical system after sufficient time has elapsed at which its composition has no measurable tendency towards further change.
The affinity constants, k + and k −, of the 1879 paper can now be recognised as rate constants. The equilibrium constant, K, was derived by setting the rates of forward and backward reactions to be equal. This also meant that the chemical affinities for the forward and backward reactions are equal. The resultant expression
where [H +] is the equilibrium concentration of H +, K a is the acid dissociation constant, C a and C b are the analytical concentrations of the acid and its conjugate base, respectively, and Δ = [H +] − [OH −]. The equation can be solved for [H +] by using the autoionization constant for water, K w, to introduce [OH −] = K w /[H +].
The free concentrations are calculated by solving the equations of mass-balance, and the concentrations of the complexes are calculated using the equilibrium constant definitions. A quantity corresponding to the observed quantity can then be calculated using physical principles such as the Nernst potential or Beer-Lambert law which relate the ...
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K c = [NH 3 (CHCl3)]/[NH 3 (aq)] (where K c is the equilibrium constant) The equilibrium concentrations of ammonia in each layer can be established by titration with standard acid solution. It can thus be determined that K c remains constant, with a value of 0.4 in this case.