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Topic: Unknown reactions  (Read 2766 times)

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Offline 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?

Online Babcock_Hall

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Re: Unknown reactions
« 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?

Offline discodermolide

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Offline Rutherford

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Re: Unknown reactions
« 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.

Offline Rutherford

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Re: Unknown reactions
« 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?

Offline discodermolide

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Re: Unknown reactions
« 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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Offline Rutherford

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Re: Unknown reactions
« 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."

Offline discodermolide

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Re: Unknown reactions
« Reply #7 on: November 03, 2012, 12:29:11 PM »
I have made this Grignard from 4-Chlorobromo benzene and reacted it with CO2, it is a great reaction.
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