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Chromate anions (CrO 2− 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 ...
"7+3" in the context of chemotherapy is an acronym for a chemotherapy regimen that is most often used today (as of 2014) as first-line induction therapy (to induce remission) in acute myelogenous leukemia, [1] [2] excluding the acute promyelocytic leukemia form, which is better treated with ATRA and/or arsenic trioxide and requires less chemotherapy (if requires it at all, which is not always ...
Commonly three electrons are added to a chromium atom, reducing it to oxidation state +3. In acid solution the aquated Cr 3+ ion is produced. Cr 2 O 2− 7 + 14 H + + 6 e − → 2 Cr 3+ + 7 H 2 O ε 0 = 1.33 V. In alkaline solution chromium(III) hydroxide is produced. The redox potential shows that chromates are weaker oxidizing agent in ...
Cr 2 O 3 + 3 CrO 3 → 5 CrO 2 + O 2. Along with many other oxides, it is used as a compound when polishing (also called stropping) the edges of knives, razors, surfaces of optical devices etc. on a piece of leather, balsa, cloth or other material. It is available in powder or wax form, and in this context it is known as "green compound".
4 HCrO 4 − + 3 RCH 2 OH + 16 H + + 11 H 2 O → 4 [Cr(H 2 O) 6] 3+ + 3 RCOOH. The inorganic products are green, characteristic of chromium(III) aquo complexes. [2] Like many other oxidations of alcohols by metal oxides, the reaction proceeds via the formation of a mixed chromate ester: [3] [4] These esters have the formula CrO 3 (OCH 2 R) −
A typical PCC oxidation involves addition of an alcohol to a suspension of PCC in dichloromethane. [6] [7] [8] The general reaction is: 2 [C 5 H 5 NH][CrO 3 Cl] + 3 R 2 CHOH → 2 [C 5 H 5 NH]Cl + Cr 2 O 3 + 3 R 2 C=O + 3 H 2 O. For example, the triterpene lupeol was oxidized to lupenone: [9]
A chromate ester is a chemical structure that contains a chromium atom (symbol Cr) in a +6 oxidation state that is connected via an oxygen (O) linkage to a carbon (C) atom. The Cr itself is in its chromate form, with several oxygens attached, and the Cr–O–C attachment makes this chemical group structurally similar to other ester functional groups.