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The hydrogen chromate ion, HCrO 4 −, is a weak acid: HCrO − 4 ⇌ CrO 2− 4 + H +; pK a ≈ 5.9. It is also in equilibrium with the dichromate ion: 2 HCrO − 4 ⇌ Cr 2 O 2− 7 + H 2 O. This equilibrium does not involve a change in hydrogen ion concentration, which would predict that the equilibrium is independent of pH.
Representative d-orbital splitting diagrams for square planar complexes featuring σ-donor (left) and σ+π-donor (right) ligands. A general d-orbital splitting diagram for square planar (D 4h) transition metal complexes can be derived from the general octahedral (O h) splitting diagram, in which the d z 2 and the d x 2 −y 2 orbitals are degenerate and higher in energy than the degenerate ...
Potassium chromate is the inorganic compound with the formula K 2 CrO 4. This yellow solid is the potassium salt of the chromate anion. It is a common laboratory chemical, whereas sodium chromate is important industrially.
The phosphite ion, PO 3− 3, is a strong base, and so always carries at least one proton. In this case the proton is attached directly to the phosphorus atom with the structure HPO 2− 3. In forming this ion, the phosphite ion is behaving as a Lewis base and donating a pair of electrons to the Lewis acid, H +. Predominance diagram for chromate
A completely polar bond is more correctly called an ionic bond, and occurs when the difference between electronegativities is large enough that one atom actually takes an electron from the other. The terms "polar" and "nonpolar" are usually applied to covalent bonds, that is, bonds where the polarity is not complete. To determine the polarity ...
Other reducing agents such as hydroperoxides can oxidize the hypochromate ion into chromate ions. [1] At extremely high temperatures, it decomposes into potassium chromate and potassium metal. [2] This compound is used to synthesize various compounds such as chromyl chlorosulfate by reacting this compound with chlorosulfuric acid. [3]
A chromate ester is a chemical structure that contains a chromium atom (symbol Cr) in a +6 oxidation state that is connected via an oxygen (O) linkage to a carbon (C) atom. The Cr itself is in its chromate form, with several oxygens attached, and the Cr–O–C attachment makes this chemical group structurally similar to other ester functional groups.
It may be formed by the salt metathesis reaction of potassium chromate and iron(III) nitrate, which gives potassium nitrate as byproduct. 2 Fe(NO 3) 3 + 3 K 2 CrO 4 → Fe 2 (CrO 4)3 + 6 KNO 3. It also can be formed by the oxidation by air of iron and chromium oxides in a basic environment: 4 Fe 2 O 3 + 6 Cr 2 O 3 + 9 O 2 → 4 Fe 2 (CrO 4) 3