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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. [2]
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. [ notes 1 ] The chromate ion is the predominant species in alkaline solutions, but dichromate can become the predominant ion in acidic solutions.
3 c 2 h 5 oh + 2 k 2 cr 2 o 7 + 8 h 2 so 4 → 3 ch 3 cooh + 2 cr 2 (so 4) 3 + 2 k 2 so 4 + 11 h 2 o The excess dichromate is determined by titration against sodium thiosulfate . Adding the amount of excess dichromate from the initial amount, gives the amount of ethanol present.
For example, [Ti(H 2 O) 6] 4+ is unknown: the hydrolyzed species [Ti(OH) 2 (H 2 O) n] 2+ is the principal species in dilute solutions. [11] With the higher oxidation states the effective electrical charge on the cation is further reduced by the formation of oxo-complexes.
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.
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This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.