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In chemistry, an acid–base reaction is a chemical reaction that occurs between an acid and a base.It can be used to determine pH via titration.Several theoretical frameworks provide alternative conceptions of the reaction mechanisms and their application in solving related problems; these are called the acid–base theories, for example, Brønsted–Lowry acid–base theory.
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 pK a − 1 or pK b − 1.
Three different points in an acid-base titration using phenolphthalein as the indicator. Phenolphthalein is widely recognized as one of the most commonly used acid-base indicators in chemistry. [12] Its popularity is because of its effectiveness in a broad pH range and its distinct colour transitions. [12]
[15] In Lewis theory an acid, A, and a base, B, form an adduct, AB, where the electron pair forms a dative covalent bond between A and B. This is shown when the adduct H 3 N−BF 3 forms from ammonia and boron trifluoride , a reaction that cannot occur in water because boron trifluoride hydrolizes in water.
Acid–base titrations depend on the neutralization between an acid and a base when mixed in solution. In addition to the sample, an appropriate pH indicator is added to the titration chamber, representing the pH range of the equivalence point. The acid–base indicator indicates the endpoint of the titration by changing color.
According to the original formulation of Lewis, when a neutral base forms a bond with a neutral acid, a condition of electric stress occurs. [7] The acid and the base share the electron pair that formerly belonged to the base. [7] As a result, a high dipole moment is created, which can only be decreased to zero by rearranging the molecules. [7]
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.
He used potentiometric titration to observe the differences in titration between strong and weak acids, as well as the behavior of polybasic acids. He introduced the idea of using potentiometric titrations for acids and bases that could not be titrated in conjunction with a colorimetric indicator [ 1 ]