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For example, acetic acid is a weak acid which has a = 1.75 x 10 −5. Its conjugate base is the acetate ion with K b = 10 −14 /K a = 5.7 x 10 −10 (from the relationship K a × K b = 10 −14), which certainly does not correspond to a strong base. The conjugate of a weak acid is often a weak base and vice versa.
On the other hand, if a chemical is a weak acid its conjugate base will not necessarily be strong. Consider that ethanoate, the conjugate base of ethanoic acid, has a base splitting constant (Kb) of about 5.6 × 10 −10, making it a weak base. In order for a species to have a strong conjugate base it has to be a very weak acid, like water.
For example, if the concentration of the conjugate base is 10 times greater than the concentration of the acid, their ratio is 10:1, and consequently the pH is pK a + 1 or pK b + 1. Conversely, if a 10-fold excess of the acid occurs with respect to the base, the ratio is 1:10 and the pH is p K a − 1 or p K b − 1.
However, for weak acids, a quadratic equation must be solved, and for weak bases, a cubic equation is required. In general, a set of non-linear simultaneous equations must be solved. Water itself is a weak acid and a weak base, so its dissociation must be taken into account at high pH and low solute concentration (see Amphoterism ).
Nitric acid, with a pK value of around −1.7, behaves as a strong acid in aqueous solutions with a pH greater than 1. [23] At lower pH values it behaves as a weak acid. pK a values for strong acids have been estimated by theoretical means. [24] For example, the pK a value of aqueous HCl has been estimated as −9.3.
Simple organic acids like formic or acetic acids are used for oil and gas well stimulation treatments. These organic acids are much less reactive with metals than are strong mineral acids like hydrochloric acid (HCl) or mixtures of HCl and hydrofluoric acid (HF). For this reason, organic acids are used at high temperatures or when long contact ...
However, the acids and bases must differ greatly in strength, e.g. one strong acid and one very weak acid. [1] Therefore, the two acids must have a pK a (or pK b) difference that is as large as possible. For example, the following can be separated: Very weak acids like phenols (pK a around 10) from stronger acids like carboxylic acids [1] (pK a ...
For example, carbon monoxide is a very weak Brønsted–Lowry base but it forms a strong adduct with BF 3. In another comparison of Lewis and Brønsted–Lowry acidity by Brown and Kanner, [ 19 ] 2,6-di- t -butylpyridine reacts to form the hydrochloride salt with HCl but does not react with BF 3 .
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