@abb0t help
I want to see the reaction (possibly mechanism) of Cyclohexanone with alkaline KMno4..
You get two carboxilic acids on the same chain. and you open the ring. The oxidation of cyclohexanone WITH potassium permanganate is actually a bit complex. I don't think you need to know it per-say.
Without an acid, this is your product. Keep in mind that ketones are inert to most oxidizing agents. This is a very slow reaction. |dw:1379100370487:dw|
I know the result too but wondering how :(
I don't think you will go over it in class. I remember it being an unusual mechanism. But I think a bridge forms? As you know, KMnO\(_4\) is an inorganic compound, and it may not be relevant (at this point in organic chemistry) to know the detailed mechamism.
You may learn it in Advance Organic or Mechanism for Organic Synthesis in upper division. Best of Luck. Cheers.
|dw:1379102404010:dw| @abb0t how do we do this?
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