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![[Post New]](/templates/default/images/icon_minipost_new.gif) 15 Jan 2008 00:10:56 IST
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find X ,give da mechanism for the rean. also
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15 Jan 2008 14:29:50 IST
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I think X shud be CH3-CH2-CH2OH.
Am I right?
It shud be simple decarboxylation, that is,CO2 escapes from COOH and it forms an alcohol.
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15 Jan 2008 15:09:37 IST
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I think Tarin is right.
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15 Jan 2008 21:51:07 IST
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nopes...
its an alpha-hydroxy acid...when heated i undergoes INTERmolecular esterification.....
keep the same molecule in front of the originalone(just like the mirror image....OH on front of COOH and COOH in front of OH)....
and just remove H2O as in the case of esterifiacation....
i hope u got it...
loss of CO2 takes lace in case of beta-keto acids and alpha-beta unsaturated acids...
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yes removal of H2O will take place
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15 Jan 2008 23:37:49 IST
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@neeraj is right
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16 Jan 2008 03:23:28 IST
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Good work Neeraj
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16 Jan 2008 13:58:53 IST
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culd u please gimme da exact structure of the product thanx
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