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One use of conjugate acids and bases lies in buffering systems, which include a buffer solution. In a buffer, a weak acid and its conjugate base (in the form of a salt), or a weak base and its conjugate acid, are used in order to limit the pH change during a titration process. Buffers have both organic and non-organic chemical applications.
An acid may also form hydrogen bonds to its conjugate base. This process, known as homoconjugation, has the effect of enhancing the acidity of acids, lowering their effective pK a values, by stabilizing the conjugate base. Homoconjugation enhances the proton-donating power of toluenesulfonic acid in acetonitrile solution by a factor of nearly 800.
The equilibrium constant for the protonation of a base, B, + H + ⇌ + is an association constant, K b, which is simply related to the dissociation constant of the conjugate acid, BH +. = The value of is ca. 14 at 25 °C. This approximation can be used when the correct value is not known.
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.
Outside the transition range the concentration of acid or conjugate base is less than 10 % and the colour of the major species dominates. Species concentrations calculated with the program HySS for a 10 mM solution of citric acid. pK a1 = 3.13, pK a2 = 4.76, pK a3 = 6.40. A weak acid may be defined as an acid with pK a greater than
For buffers in acid regions, the pH may be adjusted to a desired value by adding a strong acid such as hydrochloric acid to the particular buffering agent. For alkaline buffers, a strong base such as sodium hydroxide may be added. Alternatively, a buffer mixture can be made from a mixture of an acid and its conjugate base.
The acid, HA, is a proton donor which can lose a proton to become its conjugate base, A −. The base, B, is a proton acceptor which can become its conjugate acid, HB +. Most acid–base reactions are fast, so the substances in the reaction are usually in dynamic equilibrium with each other. [8]
In this case H 0 and H − are equivalent to pH values determined by the buffer equation or Henderson-Hasselbalch equation. However, an H 0 value of −21 (a 25% solution of SbF 5 in HSO 3 F ) [ 5 ] does not imply a hydrogen ion concentration of 10 21 mol/dm 3 : such a "solution" would have a density more than a hundred times greater than a ...