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Topic: oxidation of ketones  (Read 12523 times)

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Offline d.mahmoud

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oxidation of ketones
« on: November 22, 2007, 02:35:26 PM »
hi,
i need help to understand oxidation of ketones
either by
1- KMNO4
2-Beyer villiger
and wat is the product in each case , please
thanks



Offline smellor

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Re: oxidation of ketones
« Reply #1 on: November 22, 2007, 05:18:27 PM »
if you read the forum rules it seems that people are unlikely to give you any response unless you show at least an attempt at solving this problem yourself. additionally, most decent textbooks should cover this to some extent...

Offline Nick.Sparrow

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Re: oxidation of ketones
« Reply #2 on: November 22, 2007, 05:21:50 PM »
about Baeyer-Villiger oxidation, see

http://www.organische-chemie.ch/index3.htm?http://www.organische-chemie.ch/OC/Namen/Baeyer-Villiger.htm

In the case of KMnO4, the reaction is selective only in the cases when one of the radicals R can not be oxidated, otherwise you will heve to different acids from one Ketone
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Offline d.mahmoud

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Re: oxidation of ketones
« Reply #3 on: November 25, 2007, 01:11:09 PM »
hi
thank you for reply
i really appreciate it
but my problem is that i have seen in a book that oxidation of ketones by kmno4
give 2 molecules of carboxylic acid but i could not understand how did they formed
if some one can help me in this, i will be so gratefull
thanks,,

Offline puppy8800

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Re: oxidation of ketones
« Reply #4 on: November 26, 2007, 03:45:42 AM »
C-C bonds break, forming carboxylic acids respectively
if an asymmetric ketone is oxidized by KMnO4(H+), either C-C bond could break, and the product is usually a mixture of acids

Offline agrobert

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Re: oxidation of ketones
« Reply #5 on: November 27, 2007, 12:41:18 PM »
As in  Nick.Sparrows example, the lower reaction is an asymmetric ketone that breaks a C-C bond to make acetic acid without selectivity also yielding propanoic acid.
In the realm of scientific observation, luck is only granted to those who are prepared. -Louis Pasteur

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