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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]
Potassium dichromate, K 2 Cr 2 O 7, is a common inorganic chemical reagent, ... When an alkali is added to an orange-red solution containing dichromate ions, ...
Sodium dichromate is the inorganic compound with the formula Na 2 Cr 2 O 7. However, the salt is usually handled as its dihydrate Na 2 Cr 2 O 7 ·2 H 2 O . Virtually all chromium ore is processed via conversion to sodium dichromate and virtually all compounds and materials based on chromium are prepared from this salt. [ 1 ]
Ammonium dichromate is an inorganic compound with the formula (NH 4) 2 Cr 2 O 7. In this compound, as in all chromates and dichromates, chromium is in a +6 oxidation state, commonly known as hexavalent chromium. It is a salt consisting of ammonium ions and dichromate ions.
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 2 Cl 2). [6]
Chromic acid is jargon for a solution formed by the addition of sulfuric acid to aqueous solutions of dichromate. It consists at least in part of chromium trioxide. [3] The term chromic acid is usually used for a mixture made by adding concentrated sulfuric acid to a dichromate, which may contain a variety of compounds, including solid chromium ...
Chromyl chloride can be prepared by the reaction of potassium chromate or potassium dichromate with hydrogen chloride in the presence of concentrated sulfuric acid, followed by distillation. [3] [4] K 2 Cr 2 O 7 + 6 HCl → 2 CrO 2 Cl 2 + 2 KCl + 3 H 2 O. The sulfuric acid serves as a dehydration agent.
The formation of the divanadate ion is analogous to the formation of the dichromate ion. As the pH is reduced, further protonation and condensation to polyvanadates occur: at pH 4-6 [H 2 VO 4] − is predominant at pV greater than ca. 4, while at higher concentrations trimers and tetramers are formed.