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With specific values for C a and K a this quadratic equation can be solved for x. Assuming [4] that pH = −log 10 [H +] the pH can be calculated as pH = −log 10 x. If the degree of dissociation is quite small, C a ≫ x and the expression simplifies to = and pH = 1 / 2 (pK a − log C a).
The Henderson–Hasselbalch equation can be used to estimate the pH of a buffer solution by approximating the actual concentration ratio as the ratio of the analytical concentrations of the acid and of a salt, MA. The equation can also be applied to bases by specifying the protonated form of the base as the acid.
The equations, derived from the acidity constant and basicity constant, states that when pH equals the pK a or pK b value of the indicator, both species are present in a 1:1 ratio. If pH is above the p K a or p K b value, the concentration of the conjugate base is greater than the concentration of the acid, and the color associated with the ...
A strong acid, such as hydrochloric acid, at concentration 1 mol dm −3 has a pH of 0, while a strong alkali like sodium hydroxide, at the same concentration, has a pH of 14. Since pH is a logarithmic scale, a difference of one in pH is equivalent to a tenfold difference in hydrogen ion concentration.
pH = 1 / 2 pK w + 1 / 2 log (1 + T A / K a ) With a dilute solution of the weak acid, the term 1 + T A / K a is equal to T A / K a to a good approximation. If pK w = 14, pH = 7 + (pK a + log T A)/2. This equation explains the following facts: The pH at the end-point depends mainly on the strength of the ...
Published values for log K 1 and log K D are 5.89 and 2.05, respectively. [2] Using these values and the equality conditions, the concentrations of the three species, chromate CrO 2− 4 , hydrogen chromate HCrO − 4 and dichromate Cr 2 O 2− 7 can be calculated, for various values of pH, by means of the equilibrium expressions.
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The Hammett acidity function (H 0) is a measure of acidity that is used for very concentrated solutions of strong acids, including superacids.It was proposed by the physical organic chemist Louis Plack Hammett [1] [2] and is the best-known acidity function used to extend the measure of Brønsted–Lowry acidity beyond the dilute aqueous solutions for which the pH scale is useful.