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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]
With concentrated hydrochloric acid, it converts to chromyl chloride, which in turn reacts with water to form chromic acid and additional hydrochloric acid. When treated with 18-crown-6 , it forms the lipophilic salt [K(18-crown-6)]CrO 3 Cl.
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.
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Potassium chromate is added as indicator in an Erlenmeyer flask and the end of the reaction is determined by the slight red color given by the silver chromate. In the Mohr method, named after Karl Friedrich Mohr , potassium chromate is an indicator, giving red silver chromate after all chloride ions have reacted:
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The reactivity of the chromate anion with silver is lower than with halides (e.g. chlorides) so that in a mixture of both ions, only silver chloride precipitate will form: [9] AgNO 3(aq) + Cl − (aq) + CrO 2− 4(aq) → AgCl (s) + CrO 2− 4(aq) + NO − 3(aq) Only when no chloride (or any halogen) is left will silver chromate form and ...