Benzoic acid, 2,4,6-trimethyl-

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Phase change data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled as indicated in comments:
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DRB - Donald R. Burgess, Jr.
AC - William E. Acree, Jr., James S. Chickos

Quantity Value Units Method Reference Comment
Δsub103.6 ± 0.3kJ/molVColomina, Jimenez, et al., 1987see Colomina, Turrion, et al., 1964; ALS
Δsub103.6kJ/molN/AColomina, Jimenez, et al., 1987DRB
Δsub103.6 ± 0.3kJ/molMEColomina, Jimenez, et al., 1987Based on data from 316. to 340. K.; AC

Enthalpy of sublimation

ΔsubH (kJ/mol) Temperature (K) Method Reference Comment
102.5 ± 0.3328.MEColomina, Jimenez, et al., 1987Based on data from 316. to 340. K.; AC

Reaction thermochemistry data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: John E. Bartmess

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Individual Reactions

C10H11O2- + Hydrogen cation = Benzoic acid, 2,4,6-trimethyl-

By formula: C10H11O2- + H+ = C10H12O2

Quantity Value Units Method Reference Comment
Δr1418. ± 8.8kJ/molG+TSDecouzon, Ertl, et al., 1993gas phase; relative to benzoate at 333.0 kcal/mol
Quantity Value Units Method Reference Comment
Δr1389. ± 8.4kJ/molIMREDecouzon, Ertl, et al., 1993gas phase; relative to benzoate at 333.0 kcal/mol

Gas phase ion energetics data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: John E. Bartmess

De-protonation reactions

C10H11O2- + Hydrogen cation = Benzoic acid, 2,4,6-trimethyl-

By formula: C10H11O2- + H+ = C10H12O2

Quantity Value Units Method Reference Comment
Δr1418. ± 8.8kJ/molG+TSDecouzon, Ertl, et al., 1993gas phase; relative to benzoate at 333.0 kcal/mol
Quantity Value Units Method Reference Comment
Δr1389. ± 8.4kJ/molIMREDecouzon, Ertl, et al., 1993gas phase; relative to benzoate at 333.0 kcal/mol

UV/Visible spectrum

Go To: Top, Phase change data, Reaction thermochemistry data, Gas phase ion energetics data, References, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Victor Talrose, Alexander N. Yermakov, Alexy A. Usov, Antonina A. Goncharova, Axlexander N. Leskin, Natalia A. Messineva, Natalia V. Trusova, Margarita V. Efimkina

Spectrum

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Additional Data

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Source Smirnova, et al., 1976
Owner INEP CP RAS, NIST OSRD
Collection (C) 2007 copyright by the U.S. Secretary of Commerce
on behalf of the United States of America. All rights reserved.
Origin INSTITUTE OF ENERGY PROBLEMS OF CHEMICAL PHYSICS, RAS
Source reference RAS UV No. 17745
Instrument SF-4a
Melting point 155

References

Go To: Top, Phase change data, Reaction thermochemistry data, Gas phase ion energetics data, UV/Visible spectrum, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Colomina, Jimenez, et al., 1987
Colomina, M.; Jimenez, P.; Roux, M.V.; Turrion, C., Thermochemical properties of benzoic acid derivatives. XV. Vapour pressures and enthalpies of sublimation and formation of the six trimethylbenzoic acids, J. Chem. Thermodyn., 1987, 19, 1139-1144. [all data]

Colomina, Turrion, et al., 1964
Colomina, M.; Turrion, C.; Boned, M.L.; Panea, M., Investigaciones termoquimicas sobre los acidos alquilbenzoicos. III. Acidos trimetilbenzoicos, Anal. Fisc. Quim. B, 1964, 60, 619-626. [all data]

Decouzon, Ertl, et al., 1993
Decouzon, M.; Ertl, P.; Exner, O.; Gal, J.F.; Maria, P.C., Concepts of Sterically Hindered Resonance and Buttressing Effect - Gas-Phase Acidities of Methyl-Substituted Benzoic Acids and Basicities of, J. Am. Chem. Soc., 1993, 115, 25, 12071, https://doi.org/10.1021/ja00078a052 . [all data]

Smirnova, et al., 1976
Smirnova, T.I., et al., Zhur. Organ. Khim. (English translation), 1976, 12, 107. [all data]


Notes

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