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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 measurement of pH can become difficult at extremely acidic or alkaline conditions, such as below pH 2.5 (ca. 0.003 mol/dm 3 acid) or above pH 10.5 (above ca. 0.0003 mol/dm 3 alkaline). This is due to the breakdown of the Nernst equation in such conditions when using a glass electrode. Several factors contribute to this problem.
The logarithm keys (LOG for base 10 and LN for base e) on a TI-83 Plus graphing calculator Logarithms are easy to compute in some cases, such as log 10 (1000) = 3 . In general, logarithms can be calculated using power series or the arithmetic–geometric mean , or be retrieved from a precalculated logarithm table that provides a fixed precision.
The identities of logarithms can be used to approximate large numbers. Note that log b (a) + log b (c) = log b (ac), where a, b, and c are arbitrary constants. Suppose that one wants to approximate the 44th Mersenne prime, 2 32,582,657 −1. To get the base-10 logarithm, we would multiply 32,582,657 by log 10 (2), getting 9,808,357.09543 ...
The smaller the difference, the more the overlap. In the case of citric acid, the overlap is extensive and solutions of citric acid are buffered over the whole range of pH 2.5 to 7.5. Calculation of the pH with a polyprotic acid requires a speciation calculation to be performed. In the case of citric acid, this entails the solution of the two ...
A typical titration curve of a diprotic acid, oxalic acid, titrated with a strong base, sodium hydroxide.Both equivalence points are visible. Titrations are often recorded on graphs called titration curves, which generally contain the volume of the titrant as the independent variable and the pH of the solution as the dependent variable (because it changes depending on the composition of the ...
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The distribution coefficient, log D, is the ratio of the sum of the concentrations of all forms of the compound (ionized plus un-ionized) in each of the two phases, one essentially always aqueous; as such, it depends on the pH of the aqueous phase, and log D = log P for non-ionizable compounds at any pH.
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