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It is the acidic anhydride of chromic acid, and is sometimes marketed under the same name. [6] This compound is a dark-purple solid under anhydrous conditions and bright orange when wet. The substance dissolves in water accompanied by hydrolysis. [clarification needed] Millions of kilograms are produced annually, mainly for electroplating. [7]
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 mechanism of this process likely depends on the acidity of the chromium reagent. Acidic reagents such as PCC may cause ionization and recombination of the chromate ester (path A), while the basic reagents (Collins) likely undergo direct allylic transposition via sigmatropic rearrangement (path B).
Further condensation reactions can occur in strongly acidic solution with the formation of trichromates, Cr 3 O 2− 10, and tetrachromates, Cr 4 O 2− 13. [2] All polyoxyanions of chromium(VI) have structures made up of tetrahedral CrO 4 units sharing corners. [3] The hydrogen chromate ion, HCrO 4 −, is a weak acid: HCrO − 4 ⇌ CrO 2−
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 the hypothetical formula H 2 CrO 4. It is a vaguely described chemical, despite many well-defined ...
Chromic acid is an intermediate in chromium plating, and is also used in ceramic glazes, and colored glass. Because a solution of chromic acid in sulfuric acid (also known as a sulfochromic mixture or chromosulfuric acid) is a powerful oxidizing agent, it can be used to clean laboratory glassware, particularly of otherwise insoluble organic ...
Although insoluble in water, it reacts with acid to produce salts of hydrated chromium ions such as [Cr(H 2 O) 6] 3+. [11] It is also attacked by concentrated alkali to yield salts of [Cr(OH) 6] 3−. When heated with finely divided carbon or aluminium, it is reduced to chromium metal: Cr 2 O 3 + 2 Al → 2 Cr + Al 2 O 3
The Sarett oxidation is an organic reaction that oxidizes primary and secondary alcohols to aldehydes and ketones, respectively, using chromium trioxide and pyridine.Unlike the similar Jones oxidation, the Sarett oxidation will not further oxidize primary alcohols to their carboxylic acid form, neither will it affect carbon-carbon double bonds. [1]