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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
[notes 1] The chromate ion is the predominant species in alkaline solutions, but dichromate can become the predominant ion in acidic solutions. 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]
At 25 °C (77 °F), solutions with a pH less than 7 are acidic, and solutions with a pH greater than 7 are basic. Solutions with a pH of 7 at 25 °C are neutral (i.e. have the same concentration of H + ions as OH − ions, i.e. the same as pure water). The neutral value of the pH depends on the temperature and is lower than 7 if the temperature ...
This kind of chromic acid may be used as a cleaning mixture for glass. Chromic acid may also refer to the molecular species, H 2 CrO 4 of which the trioxide is the anhydride. Chromic acid features chromium in an oxidation state of +6 (and a valence of VI or 6). It is a strong and corrosive oxidizing agent and a moderate carcinogen.
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Chromium(II) oxide (CrO) is an inorganic compound composed of chromium and oxygen. [1] It is a black powder that crystallises in the rock salt structure. [2] Hypophosphites may reduce chromium(III) oxide to chromium(II) oxide: H 3 PO 2 + 2 Cr 2 O 3 → 4 CrO + H 3 PO 4. It is readily oxidized by the atmosphere. CrO is basic, while CrO 3 is ...