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the ortho substitute benzoic acid is more acidic than the meta and para position due to ortho effect ...its true but is it correct when benzoic acid join with +R/+I ?
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the ortho substitute benzoic acid is more acidic than the meta and par...
Yes , it's correct ,it doesn't matter whether the substitution group is -I/-R or +R/+I at the ortho postion of benzoic acid,As any of these group present at ortho postion then it changes the planarity of bezene rings w.r.t. CooH so,that COO- can't do resonance with rings and hence become more stable, as here if resources would have occur then it has decreased the stability of COO-
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the ortho substitute benzoic acid is more acidic than the meta and para position due to ortho effect ...its true but is it correct when benzoic acid join with +R/+I ?
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