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Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

Thermodynamic functions of ionization of t-butyl-substituted and methoxysubstituted phenols

PD Bolton, FM Hall and J Kudrynski

Australian Journal of Chemistry 25(1) 75 - 80
Published: 1972

Abstract

Thermodynamic ionization constants of 2-t-butylphenol, 3-t-butylphenol, 4-t-butylphenol, 3,5-di-t-butylphenol, and 3,5-dimethoxyphenol have been measured in aqueous solution by an e.m.f./spectrophotometric method within the temperature range 5-60°C and the thermodynamic functions of ionization ΔG25, ΔH25, ΔS25, and ΔCp25 calculated. These results confirm the additivity of substituent effects noted previously for the ionization of 3,5-disubstituted phenols and indicate that this ionization process is relatively insensitive to steric effects.

https://doi.org/10.1071/CH9720075

© CSIRO 1972

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