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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
It was popularized for selective oxidation of primary and secondary alcohols to carbonyl compounds. Collins reagent is a solution of the same CrO 3 (pyridine) 2 but in dichloromethane. The Ratcliffe variant of Collins reagent relates to details of the preparation of this solution, i.e., the addition of chromium trioxide to a solution of ...
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.
Pyridinium chlorochromate in a vial. Pyridinium chlorochromate (PCC) is a yellow-orange salt with the formula [C 5 H 5 NH] + [CrO 3 Cl] −.It is a reagent in organic synthesis used primarily for oxidation of alcohols to form carbonyls.
For compounds containing an oxyanion of chromium in oxidation state of +3; For other compounds of chromium(III) as a means of distinguishing a chemical species such as hexacyanochromite(III). [Cr(CN) 6] 3− from an analogous compound in which chromium is a different oxidation state. The mineral chromite is an iron chromium oxide with empirical ...
Chromate and dichromate have equal concentrations. Setting [CrO 2− 4] equal to [Cr 2 O 2− 7] in Eq. 3 gives [CrO 2− 4] = 1 / β 2 [H +] 2 . The predominance diagram is interpreted as follows. The chromate ion is the predominant species in the region to the right of the green and blue lines. Above pH ~6.75 it is always the ...
Strontium chromate is approximately 30 times more soluble in water at 100 °C than at room temperature. Therefore, the yellow strontium chromate can be suspended in a hot solution of a soluble sulfate to digest until fully converted to the much less soluble and white strontium sulfate, leaving the chromate or dichromate in solution.