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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 ]
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.
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 ...
In weak acidic medium MnO − 4 can not accept 5 electrons to form Mn 2+. Instead, it accepts only 3 electrons and forms solid MnO 2 by the following reaction: MnO − 4 + 4 H + + 3 e − → MnO 2 + 2 H 2 O; E° = +1.69 V. In a strongly basic solution, with the concentration c (NaOH) >1 mol dm −3, only one electron is accepted to produce ...
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 ...
The excess dichromate is determined by titration against sodium thiosulfate. Adding the amount of excess dichromate from the initial amount, gives the amount of ethanol present. Accuracy can be improved by calibrating the dichromate solution against a blank. One major application for this reaction is in old police breathalyzer tests.
Using the results of these experiments it was possible to construct a general mechanism for the reaction. Further work has been done to refine this mechanism since these early experiments. [23] [24] One such isotope scrambling experiment was the reaction of [2R-3 H]citrate with aconitase in the presence of 2-methyl-cis-aconitate.
The reactions are most usually carried out in test tubes into which a gel is formed that contains a dilute solution of one of the reactants.. If a hot solution of agar gel also containing a dilute solution of potassium dichromate is poured in a test tube, and after the gel solidifies a more concentrated solution of silver nitrate is poured on top of the gel, the silver nitrate will begin to ...