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clemenson reduction
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Topic: clemenson reduction (Read 7085 times)
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akabir85
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clemenson reduction
«
on:
January 11, 2005, 09:13:00 PM »
I want to know the clemenson reduction mechanism for aldehydes & jetones.
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Mitch
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Re:clemenson reduction
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Reply #1 on:
January 11, 2005, 09:25:00 PM »
I'll start you out. A radical anion is formed at the carbonyl carbon, and the ZnCl is coordinated with the oxygen.
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AWK
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Re:clemenson reduction
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Reply #2 on:
January 13, 2005, 01:25:20 AM »
The mechanism suggested in
www.organic-chemistry.ord
is quite different.
http://www.organic-chemistry.org/frames.htm?http://www.organic-chemistry.org/namedreactions/clemmensen-reduction.shtm
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AWK
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Re:clemenson reduction
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Reply #3 on:
January 13, 2005, 01:53:05 PM »
What Mitch said agrees with the mechanism on that site....
I don't know how I feel about the zinc carbene though. A little bit unusual.
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clemenson reduction