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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]
Chromate anions (CrO 2− 4) and dichromate (Cr 2 O 7 2−) anions are the principal ions at this oxidation state. They exist at an equilibrium, determined by pH: 2 [CrO 4] 2− + 2 H + ⇌ [Cr 2 O 7] 2− + H 2 O. Chromium(VI) oxyhalides are known also and include chromyl fluoride (CrO 2 F 2) and chromyl chloride (CrO
Structure of CrO(O 2) 2 (pyridine).Hydrogen atoms bonded to carbon atoms are omitted. Color code: Cr = gray, C= black, H = white, O= red, N = blue. Chromium(VI) oxide peroxide is formed by the addition of acidified hydrogen peroxide solutions to solutions of metal chromates or dichromates, such as sodium chromate or potassium dichromate.
The chromate is converted by sulfuric acid into the dichromate. [65] 4 FeCr 2 O 4 + 8 Na 2 CO 3 + 7 O 2 → 8 Na 2 CrO 4 + 2 Fe 2 O 3 + 8 CO 2 2 Na 2 CrO 4 + H 2 SO 4 → Na 2 Cr 2 O 7 + Na 2 SO 4 + H 2 O. The dichromate is converted to the chromium(III) oxide by reduction with carbon and then reduced in an aluminothermic reaction to chromium ...
pyridinium dichromate (PDC) is the pyridium salt of dichromate, [Cr 2 O 7] 2-. pyridinium chlorochromate (PCC) is the pyridinium salt of [CrO 3 Cl] −. These salts are less reactive, more easily handled, and more selective than Collins reagent in oxidations of alcohols.
Chromyl chloride can be prepared by the reaction of potassium chromate or potassium dichromate with hydrogen chloride in the presence of sulfuric acid, followed by distillation. [3] [4] K 2 Cr 2 O 7 + 6 HCl → 2 CrO 2 Cl 2 + 2 KCl + 3 H 2 O. The sulfuric acid serves as the dehydration agent.
Chromium dioxide (chromium(IV) oxide), CrO 2, which includes the hypothetical compound chromium(II) chromate; Chromium trioxide (chromium(VI) oxide), CrO 3; Chromium(VI) oxide peroxide, CrO 5; Mixed valence species, such as Cr 8 O 21
The oxide is also formed by the decomposition of chromium salts such as chromium nitrate, or by the exothermic decomposition of ammonium dichromate. (NH 4) 2 Cr 2 O 7 → Cr 2 O 3 + N 2 + 4 H 2 O. The reaction has a low ignition temperature of less than 200 °C and is frequently used in “volcano” demonstrations. [8]