Effect of substituents at the 5-position on the first and second dissociation constants of isophthalic acid
Stewart J. Gumbley, Ross J. Stewart
Abstract
Stewart J. Gumbley, Ross J. Stewart
Abstract
The dissociation constants of benzoic acid and 20 of its meta- or para-substituted derivatives and of isophthalic acid and ten of its 5-substituted derivatives have been measured in 50 wt% aqueous methanol. The Hammett ρ value for benzoic acid is 1.28; for isophthalic acid the ρ values are 1.21 (pK1) and 1.20 (pK2). The σmeta values for hydroxy and acetoxy are –0.01 and +0.29, respectively, in this system. Values for σmeta for CO2H and CO2– are calculated to be +0.28 and –0.20, respectively; however there are indications that these values are not completely structure-independent.
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The dissociation constants of benzoic acid and 20 of its meta- or para-substituted derivatives and of isophthalic acid and ten of its 5-substituted derivatives have been measured in 50 wt% aqueous methanol. The Hammett ρ value for benzoic acid is 1.28; for isophthalic acid the ρ values are 1.21 (pK1) and 1.20 (pK2). The σmeta values for hydroxy and acetoxy are –0.01 and +0.29, respectively, in this system. Values for σmeta for CO2H and CO2– are calculated to be +0.28 and –0.20, respectively; however there are indications that these values are not completely structure-independent.
Key concepts: Isophthalic acid, Benzoic acid, Chemistry, Methanol, Acid dissociation constant, Dissociation (chemistry), Dissociation constant, Aqueous solution