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![[Post New]](/templates/default/images/icon_minipost_new.gif) 9 Apr 2008 23:21:11 IST
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what is the productof the reaction CH2=CH2-Br + H2O =
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9 Apr 2008 23:27:15 IST
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CH2=CH2-OH
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9 Apr 2008 23:30:20 IST
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rite Nucleophilic attack occures..
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9 Apr 2008 23:30:55 IST
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i think the answe is CH3-CH2OH ?? rite???
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9 Apr 2008 23:38:54 IST
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Hey it should be:
CH2=CH-Br + H2O
CH2=CH-Br + H2O-------------> CH3-CH2-OH + HBr
I'm not sure about the reaction.
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<TABLE CELLSPACING="1" CELLPADDING="1" BORDER="0">
<TR><TD>
<DIV ALIGN="right">Glitter Graphics</DIV></TD></TR></TABLE>
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9 Apr 2008 23:43:16 IST
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CH2=CH-Br + H2O-------------> CH3-CH2-OH + HBr
how do u get this !!!!
explain the mechanism
as far as i am concerned, product is CH2=CH2-OH
it follows SN2 mechanism
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9 Apr 2008 23:45:43 IST
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Edited......
You may be correct arpan1.
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<TABLE CELLSPACING="1" CELLPADDING="1" BORDER="0">
<TR><TD>
<DIV ALIGN="right">Glitter Graphics</DIV></TD></TR></TABLE>
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10 Apr 2008 00:33:28 IST
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ya arpan1 is right vinylic carbocation is highly unstable hence SN2 reaction will occur also cleavage of C-C double bond will definitely not take place here
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10 Apr 2008 15:29:58 IST
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Surely all vinylic halides do not undergo substitution. So addition is answer. Probably, CH2=CH-Br + H2O --> CH3-CH(Br)-OH
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10 Apr 2008 15:30:43 IST
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And even if ur right then CH2=CH-OH <-->CH3-CHO
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11 Apr 2008 23:31:11 IST
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i agree with layman it will follow addition raction according to anti markonikoff rule it has already been asked in goiit
Rohan whats ans
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