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Topic: E1 & E2 Reactions (Read 4615 times)
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Winga
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E1 & E2 Reactions
«
on:
May 31, 2005, 04:19:32 AM »
e.g.
(Me)
3
C-Br + KOH + ethanol + heat <=> alkenes + KBr
Which mechanism is dominant, E1 or E2?
Is there any effect on eliminations using polar protic solvent when strong base is used?
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AWK
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Re:E1 & E2 Reactions
«
Reply #1 on:
May 31, 2005, 05:01:16 AM »
http://www.chemhelper.com/e1.html
http://www.chemhelper.com/e2.html
http://www.csupomona.edu/~fxflores/chm314_transparencies/Elimination_Reaction_Mechanisms.pdf
http://www.xula.edu/chemistry/organic/Drillbook/O06SNandE.pdf
«
Last Edit: May 31, 2005, 05:07:35 AM by AWK
»
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AWK
Winga
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Posts: 510
Mole Snacks: +39/-10
Re:E1 & E2 Reactions
«
Reply #2 on:
May 31, 2005, 06:44:19 AM »
Thank you very much!
But I still want to know the reason why polar protic solvent doesn't affect E1 and E2 reactions.
It can stabilize the carbocation in E1 and shielding the base (reduces basicity) in E2.
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