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Topic: Unknown reactions (Read 2766 times)
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Rutherford
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Unknown reactions
«
on:
November 02, 2012, 01:03:56 PM »
Can someone rationalize the two conversions as I see them for the first time?
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Babcock_Hall
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Re: Unknown reactions
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Reply #1 on:
November 02, 2012, 01:05:00 PM »
In the first reaction, which carbon is partially positively charged, and which one is partially negatively charged?
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discodermolide
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Re: Unknown reactions
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Reply #2 on:
November 02, 2012, 01:11:26 PM »
Have a look here,
http://www.chemguide.co.uk/organicprops/haloalkanes/grignard.html
and here for the second part
http://www.chemtube3d.com/Carbenes-MethylationCarboxylicAcidDiazomethane.html
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Rutherford
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Re: Unknown reactions
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Reply #3 on:
November 02, 2012, 02:07:36 PM »
Everything clear. I suppose that an alternative way for the 2nd reaction would be esterification. Thanks again.
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Rutherford
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Re: Unknown reactions
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Reply #4 on:
November 03, 2012, 11:26:41 AM »
I got another quick question related to this problem: Why is it better to produce 4-chlorobenzoic acid from chlorobenzene the way that is listed here, than using Friedel-C. alkylation and then oxidation?
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discodermolide
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Re: Unknown reactions
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Reply #5 on:
November 03, 2012, 12:20:48 PM »
The Grignard reaction is much more efficient.
Chlorine is a para director as far as I remember. Using an FC reaction will give mixtures.
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Rutherford
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Re: Unknown reactions
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Reply #6 on:
November 03, 2012, 12:26:25 PM »
It has to be so that the Grignard reaction work and I found on wikkipedia: "Halogens are ortho/para directors, since they possess an unshared pair of electrons."
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discodermolide
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Re: Unknown reactions
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Reply #7 on:
November 03, 2012, 12:29:11 PM »
I have made this Grignard from 4-Chlorobromo benzene and reacted it with CO
2
, it is a great reaction.
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