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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]
Although insoluble in water, it reacts with acid to produce salts of hydrated chromium ions such as [Cr(H 2 O) 6] 3+. [10] 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
It is readily oxidized by the atmosphere. CrO is basic, while CrO 3 is acidic, and Cr 2 O 3 is amphoteric. [3] CrO occurs in the spectra of luminous red novae, which occur when two stars collide. It is not known why red novae are the only objects that feature this molecule; one possible explanation is an as-yet-unknown nucleosynthesis process. [4]
Perbromic acid – HBrO 4 [161] Aluminium Bromide – AlBr 3 [11] Ammonium bromide – NH 4 Br [37] Boron tribromide – BBr 3 [146] Bromic acid – HBrO 3 [162] Bromine monoxide – Br 2 O [163] Bromine pentafluoride – BrF 5 [164] Bromine trifluoride – BrF 3 [165] Bromine monofluoride – BrF [166] Calcium bromide – CaBr 2 [167] Carbon ...
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−
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