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The hydrogen chromate ion, HCrO 4 −, is a weak acid: HCrO − 4 ⇌ CrO 2− 4 + H +; pK a ≈ 5.9. It is also in equilibrium with the dichromate ion: 2 HCrO − 4 ⇌ Cr 2 O 2− 7 + H 2 O. This equilibrium does not involve a change in hydrogen ion concentration, which would predict that the equilibrium is independent of pH.
The change in equilibrium is visible by a change from yellow (chromate) to orange (dichromate), such as when an acid is added to a neutral solution of potassium chromate. At yet lower pH values, further condensation to more complex oxyanions of chromium is possible. Both the chromate and dichromate anions are strong oxidizing reagents at low pH ...
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 generally yellow chromates or orange ...
As pH rises the chromate ion becomes ever more predominant, until it is the only species in solutions with pH > 6.75. At pH < pK 1 the hydrogen chromate ion, HCrO − 4 is predominant in dilute solution. The dichromate ion, Cr 2 O 2− 7, is predominant in more concentrated solutions, except at high pH.
The second family of reagents are salts, featuring the pyridinium cation (C 5 H 5 NH +). 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 ...
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 ...
Basic chromium sulfate is produced from chromate salts by reduction with sulfur dioxide, although other methods exist. [4] [5] The reduction could formally be written: Na 2 Cr 2 O 7 + 3 SO 2 + H 2 O → Cr 2 (SO 4) 3 + 2 NaOH. Since 33% of the anion charges are due to hydroxy ions the basicity is 33% (but in tanning jargon it is known as 33% ...
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. [9]