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Topic: E and Z configurations of 2-Chlorobutenedioc  (Read 5534 times)

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nemzy

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E and Z configurations of 2-Chlorobutenedioc
« on: November 21, 2004, 08:47:17 PM »
why is that a (Z)-2-chlorobutenedioc acid reacts MUCh faster than a (E)- configuration?
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Offline movies

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Re:E and Z configurations of 2-Chlorobutenedioc
« Reply #1 on: November 22, 2004, 01:13:59 PM »
In what reaction?
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puru

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Re:E and Z configurations of 2-Chlorobutenedioc
« Reply #2 on: February 02, 2005, 10:12:51 AM »
hey buddy
the Z isomer has close carbonyl groups making the other atoms along the C=C stable.
This may just be a possible reason,please check it with Mitch
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Offline Mitch

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Re:E and Z configurations of 2-Chlorobutenedioc
« Reply #3 on: February 02, 2005, 11:35:46 AM »
Need a bit more info.
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dexangeles

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Re:E and Z configurations of 2-Chlorobutenedioc
« Reply #4 on: February 03, 2005, 12:29:18 AM »
yup, definitely need more info :-\
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