Issue 3, 1984

Effect of substituents at the 5-position on the first and second dissociation constants of isophthalic acid

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.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1984, 529-531

Effect of substituents at the 5-position on the first and second dissociation constants of isophthalic acid

S. J. Gumbley and R. Stewart, J. Chem. Soc., Perkin Trans. 2, 1984, 529 DOI: 10.1039/P29840000529

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements