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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.
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.
Electron configuration is also a major factor, illustrated by the fact that the rates of water exchange for [Al(H 2 O) 6] 3+ and [Ir(H 2 O) 6] 3+ differ by a factor of 10 9 also. [4] Water exchange usually follows a dissociative substitution pathway, so the rate constants indicate first order reactions.
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