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When heated strongly, it decomposes with the evolution of oxygen. 4 K 2 Cr 2 O 7 → 4 K 2 CrO 4 + 2 Cr 2 O 3 + 3 O 2 When an alkali is added to an orange-red solution containing dichromate ions, a yellow solution is obtained due to the formation of chromate ions ( CrO 2− 4 ).
Two crystalline forms are known, both being very similar to the corresponding potassium sulfate. Orthorhombic β-K 2 CrO 4 is the common form, but it converts to an α-form above 666 °C. [ 1 ] These structures are complex, although the chromate ion adopts the typical tetrahedral geometry.
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
Predominance diagram for chromate. In aqueous solution, chromate and dichromate anions exist in a chemical equilibrium.. 2 CrO 2− 4 + 2 H + ⇌ Cr 2 O 2− 7 + H 2 O. The predominance diagram shows that the position of the equilibrium depends on both pH and the analytical concentration of chromium.
When water is heated to well over 2,000 °C (2,270 K; 3,630 °F), a small percentage of it will decompose into OH, monatomic oxygen, monatomic hydrogen, O 2, and H 2. [3] The compound with the highest known decomposition temperature is carbon monoxide at ≈3870 °C (≈7000 °F). [citation needed]
Many minerals are assumed to form via olation. Aquo ions of divalent metal ions are less acidic than those of trivalent cations. The hydrolyzed species often exhibit very different properties from the precursor hexaaquo complex. For example, water exchange in [Al(H 2 O) 5 OH] 2+ is 20000 times faster than in [Al(H 2 O) 6] 3+.
Under acidic conditions water binds to the surface with the irreversible removal of one electron and one proton to form a platinum hydroxide. [4] In an alkaline solution a reversible binding of hydroxide ion coupled to a one electron oxidation is thought to precede a turnover-limiting electrochemical step involving the removal of one proton and ...
The standard Gibbs free energy of formation (G f °) of a compound is the change of Gibbs free energy that accompanies the formation of 1 mole of a substance in its standard state from its constituent elements in their standard states (the most stable form of the element at 1 bar of pressure and the specified temperature, usually 298.15 K or 25 °C).