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Organic Chemistry
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dheer Bhatia
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Joined: 15 May 2007
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1 Apr 2008 10:14:35 IST
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meta is least then para than ortho max
reason; thre is intramolecular h bonding in ortho but in para itz intermolecular
hope u got it
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cheers!!!
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1 Apr 2008 10:25:21 IST
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Acidity of substituted phenols depends on the stability of the phenoxide anion.Thus according to the stability of anion o- > p- > m-derivative for -R or -I groups.
But in case of stability of Nitrophenols the experimental result is that p-derivative is more acidic than o-derivative which is more acidic than m-derivative.The reason is that in o-derivative the Hydrogen attached to Oxygen is in Hydrogen Bonding with Nitrogen which decreases acidity.Thus the order of acidity is para > ortho > meta-Nitrophenol.
For more details check the pKa values online.
But in case of stability of Nitrophenols the experimental result is that p-derivative is more acidic than o-derivative which is more acidic than m-derivative.The reason is that in o-derivative the Hydrogen attached to Oxygen is in Hydrogen Bonding with Nitrogen which decreases acidity.Thus the order of acidity is para > ortho > meta-Nitrophenol.
For more details check the pKa values online.











