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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 ·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 ]
Treatment with periodic acid (dioxane) and piperidine acetate (benzene) gave aldehyde 24 through diol 22 (oxidation) and dialdehyde 23 (aldol condensation). Sodium dichromate oxidation gave carboxylic acid 25 , Diazomethane treatment gave methyl ester 26 and sodium borohydride the allyl alcohol 27 .
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 ...
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.
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]
Sodium dichromate is often required as an additive to oxidise the chromium in certain 'types' of nitric-based acid baths, however this chemical is highly toxic. With citric acid, simply rinsing and drying the part and allowing the air to oxidise it, or in some cases the application of other chemicals, is used to perform the passivation of the ...
Because the hydrolysis of sodium is rapid, not to mention dangerous, the Bouveault-Blanc reaction requires anhydrous ethanol and can give low yields with insufficiently dry ethanol. [9] [8] The mechanism of the reaction follows: [1] Consistent with this mechanism, sodium-ethanol mixtures will also reduce ketones to alcohols. [10]