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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 ·2H 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]
Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.
[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]
Chromium trioxide is generated by treating sodium dichromate with sulfuric acid: [6] H 2 SO 4 + Na 2 Cr 2 O 7 → 2 CrO 3 + Na 2 SO 4 + H 2 O. Approximately 100,000 tonnes are produced annually by this or similar routes. [7] The solid consists of chains of tetrahedrally coordinated chromium atoms that share vertices.
For lab and small scale preparations a mixture of chromite ore, sodium hydroxide and sodium nitrate reacting at lower temperatures may be used (even 350 C in the corresponding potassium chromate system). [2] Subsequent to its formation, the chromate salt is converted to sodium dichromate, the precursor to most chromium compounds and materials. [3]
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 ...
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Enones can be synthesized from tertiary allylic alcohols through the action of a variety of chromium(VI)-amine reagents, in a reaction known as the Babler oxidation. The reaction is driven by the formation of a more substituted double bond. (E)-Enones form in greater amounts than (Z) isomers because of chromium-mediated geometric isomerization ...