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P 4 + 4 OH − + 4 H 2 O → 4 H 2 PO − 2 + 2 H 2. Any phosphites produced in this step can be selectively precipitated out by treatment with calcium salts. The purified material is then treated with a strong, non-oxidizing acid (often sulfuric acid) to give the free hypophosphorous acid: H 2 PO − 2 + H + → H 3 PO 2. HPA is usually ...
Solid HP(O)(OH) 2 has tetrahedral geometry about the central phosphorus atom, with a P−H bond of 132 pm, one P=O double bond of 148 pm and two longer P−OH single bonds of 154 pm. In common with other phosphorus oxides with P−H bonds (e.g. hypophosphorous acid and dialkyl phosphites ), [ 2 ] it exists in equilibrium with an extremely minor ...
The general formula of a phosphoric acid is H n+2−2x P n O 3n+1−x, where n is the number of phosphorus atoms and x is the number of fundamental cycles in the molecule's structure, between 0 and n + 2 / 2 . Pyrophosphate anion. Trimethyl orthophosphate.
Ca 5 (PO 4) 3 OH + 5 H 2 SO 4 → 3 H 3 PO 4 + 5 CaSO 4 + H 2 O Ca 5 (PO 4) 3 F + 5 H 2 SO 4 → 3 H 3 PO 4 + 5 CaSO 4 + HF. Calcium sulfate (gypsum, CaSO 4) is a by-product, which is removed as phosphogypsum. The hydrogen fluoride (HF) gas is streamed into a wet (water) scrubber producing hydrofluoric acid. In both cases the phosphoric acid ...
For many substances, the formation reaction may be considered as the sum of a number of simpler reactions, either real or fictitious. The enthalpy of reaction can then be analyzed by applying Hess' law, which states that the sum of the enthalpy changes for a number of individual reaction steps equals the enthalpy change of the overall reaction.
It is a conjugate acid of phosphate [PO 4] 3-and a conjugate base of dihydrogen phosphate [H 2 PO 4] −. It is formed when a pyrophosphate anion [P 2 O 7] 4− reacts with water H 2 O by hydrolysis, which can give hydrogenphosphate: [P 2 O 7] 4− + H 2 O ⇌ 2 [HPO 4] 2−
In acid catalysis and base catalysis, a chemical reaction is catalyzed by an acid or a base. By Brønsted–Lowry acid–base theory, the acid is the proton (hydrogen ion, H +) donor and the base is the proton acceptor. Typical reactions catalyzed by proton transfer are esterifications and aldol reactions.
Its solubility product K sp of 5.02 × 10 −6 at 25 °C, [1] its dissociation in water is large enough that its solutions are basic according to the following dissolution reaction: Ca(OH) 2 → Ca 2+ + 2 OH −. The solubility is affected by the common-ion effect. Its solubility drastically decreases upon addition of hydroxide or calcium sources.