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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]
4 CrO 3 → 2 Cr 2 O 3 + 3 O 2. It is used in organic synthesis as an oxidant, often as a solution in acetic acid, [9] or acetone in the case of the Jones oxidation. In these oxidations, the Cr(VI) converts primary alcohols to the corresponding carboxylic acids and secondary alcohols to ketones. The reactions are shown below: Primary alcohols ...
The Pourbaix diagram for chromium in pure water, perchloric acid, or sodium hydroxide [27] [28] Chromium is a member of group 6, of the transition metals. The +3 and +6 states occur most commonly within chromium compounds, followed by +2; charges of +1, +4 and +5 for chromium are rare, but do nevertheless occasionally exist. [29] [30]
2 cro(o 2) 2 + 7 h 2 o 2 + 6 h + → 2 cr 3+ + 10 h 2 o + 7 o 2 Stable adducts of the type CrO(O 2 ) 2 L include those with L = diethyl ether , 1-butanol , ethyl acetate , or amyl acetate . They form by adding a layer of the organic solvent above the chromate/dichromate solution and shaking during the addition of hydrogen peroxide.
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− 4 + H +; pK a ≈ 5.9. It is also in equilibrium with the dichromate ion: 2 HCrO − 4 ⇌ Cr 2 O 2− 7 + H 2 O
The Parisians Pannetier and Binet first prepared the transparent hydrated form of Cr 2 O 3 in 1838 via a secret process, sold as a pigment. [7] It is derived from the mineral chromite, (Fe,Mg)Cr 2 O 4. The conversion of chromite to chromia proceeds via Na 2 Cr 2 O 7, which is reduced with sulfur at high temperatures: [8] Na 2 Cr 2 O 7 + S → ...
The pentahydrate CrSO 4 ·5H 2 O is a blue solid that dissolves readily in water. Solutions of chromium(II) are easily oxidized by air to Cr(III) species. Solutions of Cr(II) are used as specialized reducing agents of value in organic synthesis. [1] The salt is produced by treating chromium metal with aqueous sulfuric acid: [2]
The reaction stoichiometry implicates the Cr(IV) species "CrO 2 OH −", which comproportionates with the chromic acid to give a Cr(V) oxide, which also functions as an oxidant for the alcohol. [ 6 ] The oxidation of the aldehydes is proposed to proceed via the formation of hemiacetal -like intermediates, which arise from the addition of the O ...