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Oxidation of phenylethanal

  • Thread starter crays
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  • #1
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Hi guys, my teacher once told me that if there's a benzene with a side chain which has a carbon group (e.g. aniline or benzaldehyde or 3-phenylpropane) it will be oxidise into benzoic acid, no matter what it is.

So my question now is, does oxidising phenylethanal gives me benzoic acid? or say even longer side chain like hipuric acid, will it be oxidised into benzoic acid too?

Another small question is that, will PCl5 react with a carbonyl say propanone?

Thanks a bunch =D
 

Answers and Replies

  • #2
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Anyone can please give me an answer?
 
  • #3
chemisttree
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You can't even begin to answer this question unless you show some work. What oxidation conditions are you given?

BTW, http://en.wikipedia.org/wiki/Aniline" [Broken] doesn't have a carbon side chain.
 
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