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A tribasic, or triprotic acid, containing three potential protons to donate; A tribasic salt, with three hydrogen atoms, with respect to the parent acid, ...
3), a triprotic acid. It forms orthophosphate salt and esters, commonly called phosphates. The smallest compounds of this class with two or more phosphorus atoms are called "oligophosphoric acids", and the larger ones, with linear –P–O– backbones, are "polyphosphoric acids"; with no definite separation between the two.
Phosphoric acid units can be bonded together in rings (cyclic structures). The simplest such compound is trimetaphosphoric acid or cyclo-triphosphoric acid having the formula H 3 P 3 O 9. Its structure is shown in the illustration. Since the ends are condensed, its formula has one less H 2 O (water) than tripolyphosphoric acid.
Peroxymonophosphoric acid is a colorless, viscous liquid. It is stabilized by an intramolecular hydrogen bond. [6] The compound is a triprotic acid with acid dissociation constants pK a1 = 1.1, pK a2 = 5.5 and pK a3 = 12.8. In aqueous solutions it slowly undergoes hydrolysis to hydrogen peroxide and phosphoric acid. [7] H 3 PO 5 + H 2 O → H 3 ...
The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.
Citric acid also dissolves in absolute (anhydrous) ethanol (76 parts of citric acid per 100 parts of ethanol) at 15 °C. It decomposes with loss of carbon dioxide above about 175 °C. Citric acid is a triprotic acid, with pK a values, extrapolated to zero ionic strength, of 3.128, 4.761, and 6.396 at 25 °C. [21]
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Lysine (symbol Lys or K) [2] is an α-amino acid that is a precursor to many proteins.Lysine contains an α-amino group (which is in the protonated −NH + 3 form when the lysine is dissolved in water at physiological pH), an α-carboxylic acid group (which is in the deprotonated −COO − form when the lysine is dissolved in water at physiological pH), and a side chain (CH 2) 4 NH 2 (which ...