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Author: Subject: oxidation of acetone
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[*] posted on 2-6-2002 at 05:19
oxidation of acetone


does any one knows some good non acid catalysts that helps the oxidation of acetone from hydrogen peroxide?
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[*] posted on 2-6-2002 at 08:19


Oxidation of acetone is very difficult; even agents like KMnO4 will not oxidize it. The reason is because oxidation of acetone requires the destruction of the carbon skeleton of the acetone molecule.



I weep at the sight of flaming acetic anhydride.
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[*] posted on 3-6-2002 at 11:46


KMnO4 easily oxidizes acetone at room temperature under strongly alkaline conditions, forming CO2 and acetic and oxalic acids. Do you want to form peroxides of acetone or oxidize it? You might try some Lewis acids - unless you consider them to be "acid catalysts." Some FeCl3 might help the reaction along. SnCl4 catalyzes the formation of a 4th peroxide of acetone. 50% H2O2 with acetone will yield a peroxide at room temperature without any acid - but it will not be the common trimeric form that people usually strive after for explosive purposes.
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[*] posted on 4-6-2002 at 11:52


I'd just like to clarify on my post: when I spoke of oxidation of acetone being difficult, I was referring to neutral conditions. :-)



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[*] posted on 10-4-2011 at 16:45


Manganese heptoxide would definitely oxidize it.



Wake up and smell the 2-furfuryl mercaptan.
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[*] posted on 10-4-2011 at 19:13


Yes, in a most explosive way. :P



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[*] posted on 10-4-2011 at 19:30


Whoaaa a 9 year necropost and madscientist is still here!



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