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For weak acid solutions, it depends on the degree of dissociation, which may be determined by an equilibrium calculation. For concentrated solutions of acids, especially strong acids for which pH < 0, the value is a better measure of acidity than the pH.
In general, organic acids are weak acids and do not dissociate completely in water, whereas the strong mineral acids do. Lower molecular mass organic acids such as formic and lactic acids are miscible in water, but higher molecular mass organic acids, such as benzoic acid, are insoluble in molecular (neutral) form.
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 .
In water, measurable pK a values range from about −2 for a strong acid to about 12 for a very weak acid (or strong base). A buffer solution of a desired pH can be prepared as a mixture of a weak acid and its conjugate base. In practice, the mixture can be created by dissolving the acid in water, and adding the requisite amount of strong acid ...
Mineral acids range from superacids (such as perchloric acid) to very weak ones (such as boric acid). Mineral acids tend to be very soluble in water and insoluble in organic solvents. Mineral acids are used in many sectors of the chemical industry as feedstocks for the synthesis of other chemicals, both organic and inorganic.
List of acids by Hammett acidity Name Hammett acidity Ref Trifluoroacetic acid-2.7 [1] Phosphoric acid-4.66 [2] Nitric acid-6.3 [3] Methanesulfonic acid-7.86 [2]
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 ...
The higher the proton affinity, the stronger the base and the weaker the conjugate acid in the gas phase.The (reportedly) strongest known base is the ortho-diethynylbenzene dianion (E pa = 1843 kJ/mol), [3] followed by the methanide anion (E pa = 1743 kJ/mol) and the hydride ion (E pa = 1675 kJ/mol), [4] making methane the weakest proton acid [5] in the gas phase, followed by dihydrogen.