Benzoic acid, 4-methoxy-

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Condensed phase 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 as indicated in comments:
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DH - Eugene S. Domalski and Elizabeth D. Hearing

Quantity Value Units Method Reference Comment
Δfsolid-134.2 ± 0.31kcal/molCcbColomina, Jimenez, et al., 1978ALS
Quantity Value Units Method Reference Comment
Δcsolid-891.42 ± 0.18kcal/molCcbColomina, Jimenez, et al., 1978Corresponding Δfsolid = -134.25 kcal/mol (simple calculation by NIST; no Washburn corrections); ALS

Constant pressure heat capacity of solid

Cp,solid (cal/mol*K) Temperature (K) Reference Comment
49.00323.Satoh and Sogabe, 1941T = 0 to 100 C. Mean value.; DH

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

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.

Individual Reactions

C8H7O3- + Hydrogen cation = Benzoic acid, 4-methoxy-

By formula: C8H7O3- + H+ = C8H8O3

Quantity Value Units Method Reference Comment
Δr340.8 ± 2.1kcal/molG+TSYamdagni, McMahon, et al., 1974gas phase
Quantity Value Units Method Reference Comment
Δr333.8 ± 2.0kcal/molIMREYamdagni, McMahon, et al., 1974gas phase

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 as indicated in comments:
B - John E. Bartmess
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

Ionization energy determinations

IE (eV) Method Reference Comment
9.0 ± 0.2EIBenoit, 1973LLK

Appearance energy determinations

Ion AE (eV) Other Products MethodReferenceComment
C7H7O+12.8 ± 0.2COOHEIBenoit, 1973LLK
C8H7O2+12.5 ± 0.2OHEIBenoit, 1973LLK

De-protonation reactions

C8H7O3- + Hydrogen cation = Benzoic acid, 4-methoxy-

By formula: C8H7O3- + H+ = C8H8O3

Quantity Value Units Method Reference Comment
Δr340.8 ± 2.1kcal/molG+TSYamdagni, McMahon, et al., 1974gas phase; B
Quantity Value Units Method Reference Comment
Δr333.8 ± 2.0kcal/molIMREYamdagni, McMahon, et al., 1974gas phase; B

References

Go To: Top, Condensed phase thermochemistry data, Reaction thermochemistry data, Gas phase ion energetics data, 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., 1978
Colomina, M.; Jimenez, P.; Roux, M.V.; Turrion, C., Thermochemical properties of benzoic acid derivatives VII. Enthalpies of combustion and formation of the o-, m-, and p-methoxy-benzoic acids, J. Chem. Thermodyn., 1978, 10, 661-665. [all data]

Satoh and Sogabe, 1941
Satoh, S.; Sogabe, T., The heat capacities of some organic compounds containing nitrogen and the atomic heat of nitrogen. (3), Sci., Pap. Inst. Phys. Chem. Res. (Tokyo), 1941, 38, 238-245. [all data]

Yamdagni, McMahon, et al., 1974
Yamdagni, R.; McMahon, T.B.; Kebarle, P., Substituent Effects on the Intrinsic Acidities of Benzoic Acids Determined by Gas Phase Proton Transfer Equilibria Measurements, J. Am. Chem. Soc., 1974, 96, 12, 4035, https://doi.org/10.1021/ja00819a063 . [all data]

Benoit, 1973
Benoit, F., Substituent effects in mass spectrometry. III. Substituent effects in the dissociation of the molecular ions of para and meta subtituted benzoic acids, Org. Mass Spectrom., 1973, 7, 295. [all data]


Notes

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