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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]
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.
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.
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.
Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75
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