organic reactions5

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#Chemistry #Organic Chemistry

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7 Answers

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Honey Arora ·2009-05-01 22:48:53

CH₂OH group wld be transformed to CH₂Cl

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JOHNCENA IS BACK ·2009-05-01 22:49:56

REMEMBER IN ORGANIC CHEMISTRY XPLANATION MATTERS NOT THE ANSWER

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JOHNCENA IS BACK ·2009-05-02 02:54:42

ne one explain!!!!!!!!!!!!!!!

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gordo ·2009-05-02 03:01:09

H+ from the HCl protonates the OH attached to the CH2OH , OH2+ leaves as H2O...a carbocation developes on the CH2+ group, and Cl- attacks to give the CH2Cl....only if theres no wierd effect or some neighbouring group effect coming into play..., a very very minor product mite be the substitution of OH directly attached to the ring, by the Cl, but dats very rare, so u cud as well rule it out....
cheers!!

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JOHNCENA IS BACK ·2009-05-03 02:56:54

hmmmmmmmm.......but don u think -OH being a activating group will resist side chain halogenation...n we will get this product

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JOHNCENA IS BACK ·2009-05-04 03:28:45

srinath...........plz reply!!!!

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voldy ·2009-05-04 04:16:55

gordo has given explanation da . write the mechanism yourself

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Your Answer

Basic Integral Calculus Operators Symbols Matrix Cases

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