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Do our students really understand the Hammett equation?

Journal of Chemical Education, 1993
In this author's experience, many students can proceed through text questions dealing with the Hammett equation without having a full understanding of the Hammett analysis. He offers a question that enables students to gain a better appreciation of this concept.
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ChemInform Abstract: The Prehistory of the Hammett Equation

ChemInform, 2000
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
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Quantitative structure–retention relationships of phenolic compounds without Hammett’s equations

Journal of Chromatography A, 2003
Retention times of phenolic compounds in a given pH eluent in reversed-phase liquid chromatography were predicted from dissociation constants derived from atomic partial charges and log P-values calculated by a computational chemical method. The precision of the calculation of atomic partial charges by AMI and PM3 methods of MOPAC was evaluated.
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Class Projects in Physical Organic Chemistry: The Hammett Equation

Journal of Chemical Education, 2001
This paper provides a brief introduction to the Hammett equation. A laboratory experiment is described that requires students to determine the pKa of three para-substituted phenols through the use of UV-spectroscopy. A student's individual data are combined with other students' data to provide a class set.
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A relationship between dipole moments and the Hammett equation

Recueil des Travaux Chimiques des Pays-Bas, 1957
AbstractAn empirical formula is proposed relating the constant ω in the Hammett equation to the observed dipole moment of a compound (para‐ or meta‐ C6H4XY). This relationship is checked by using data which have been cited in the literature. These data appear to confirm the proposed linear behaviour when log μ is plotted against σ.
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Theoretical Considerations Concerning Hammett's Equation. IV. Calculation of ρ-Values

The Journal of Chemical Physics, 1953
The assumption is made that the effect of a meta or para substituent X on the reactivity of a reacting center Y in a compound [Complex chemical formula] depends only on the electron density change induced by the substituent in the atom at which Y is attached to R.
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On Hepler’s Treatment of the Hammett Equation

Zeitschrift für Physikalische Chemie, 1974
D. K. Hazra, S. C. Lahiri
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