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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 66 °C. [1] These structures are complex, although the chromate ion adopts the typical tetrahedral geometry. [2]
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The hydrogen chromate ion may be protonated, with the formation of molecular chromic acid, H 2 CrO 4, but the pK a for the equilibrium H 2 CrO 4 ⇌ HCrO − 4 + H + is not well characterized. Reported values vary between about −0.8 and 1.6. [4] The dichromate ion is a somewhat weaker base than the chromate ion: [5]
CrO 2− 4 + 4 H 2 O + 3 e − → Cr(OH) 3 + 5 OH − (ε 0 = −0.13 V) Sodium chromate (Na 2 CrO 4) Chromium(VI) compounds in solution can be detected by adding an acidic hydrogen peroxide solution. The unstable dark blue chromium(VI) peroxide (CrO 5) is formed, which can be stabilized as an ether adduct CrO 5 ·OR 2. [6] Chromic acid has ...
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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.
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