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Chromium trioxide (also known as chromium(VI) oxide or chromic anhydride) is an inorganic compound with the formula CrO 3. 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 ...
Chromium(III) oxide is amphoteric. 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 ...
Chromium oxide may refer to: Chromium(II) oxide, CrO; Chromium(III) oxide, Cr 2 O 3; 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
Chlorine trioxide – ClO 3; Chlorine trioxide – ClO 3; Chloroplatinic acid – H 2 [PtCl 6] Chlorosulfonic acid – ClSO 3 H; Chlorosulfonyl isocyanate – ClSO 2 NCO; Chloryl fluoride – ClO 2 F; Chromium(II) chloride – CrCl 2; Chromium(III) chloride – CrCl 3; Chromyl chloride – CrO 2 Cl 2; Cisplatin (cis–platinum(II) chloride ...
A trioxide is a compound with three oxygen atoms. For metals with the M 2 O 3 formula there are several common structures. Al 2 O 3 , Cr 2 O 3 , Fe 2 O 3 , and V 2 O 3 adopt the corundum structure .
Collins reagent is the complex of chromium(VI) oxide with pyridine in dichloromethane. [2] This metal-pyridine complex, a red solid, is used to oxidize primary alcohols to the corresponding aldehydes and secondary alcohols to the corresponding ketones. This complex is a hygroscopic orange solid. [1]
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]
The Phillips catalyst is prepared by impregnating high surface area silica gel with chromium trioxide or related chromium compounds. The solid precatalyst is then calcined in air to give the active catalyst. Only a fraction of the chromium is catalytically active, a fact that interferes with elucidation of the catalytic mechanism.