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![[Post New]](/templates/default/images/icon_minipost_new.gif) 15 Jun 2007 06:56:05 IST
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1, which is weakest acid a. acitic acid b, farmic acid c, oxalic acid d. no them virendera dwivedi
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virendera dwivedi |
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![[Post New]](/templates/default/images/icon_minipost_new.gif) 15 Jun 2007 07:46:46 IST
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acetic acid is the weakest because of +I ch3 group and hence no charge dispersal takes place in the anion(acetate ion) thereby rendering it unstable. Always remember: more stable the anion,more stronger is the acid. Plz. rate me if u find this useful. 
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![[Post New]](/templates/default/images/icon_minipost_new.gif) 15 Jun 2007 08:11:18 IST
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Strength of an acid is directly proportional to -I effect of the group attached to the acyl carbanion.This is so because -I group decreses the -ve charge on the carbanion making it more stable. so according to this order of stablity is oxalic acid > formic acid > acetic acid.
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![[Post New]](/templates/default/images/icon_minipost_new.gif) 15 Jun 2007 08:50:58 IST
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Oxalic Acid > Formic Acid > Benzoic Acid > Acetic Acid
Refer to this thread for more info.
http://www.goiit.com/posts/list/organic-chemistry-arranging-of-given-compunds-according-to-their-16858.htm
And an advice - Check out your spellings ;).
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![[Post New]](/templates/default/images/icon_minipost_new.gif) 15 Jun 2007 14:47:23 IST
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aravindh is correct.. Acetic acid is the weakest, due to the electron donating tendency of the sigma bond b/w the C of methy and -COOH in formic acid, there is no electron donating group, while in acetic acid, the two -COOH groups act as electron withdrawing group for each other, thus increasing the acidity..
electron withdawing groups increases the polarity of the O-H bond and thus increases the acidity, while electron releasing groups does the opposite.
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