Acetic acid, dichloro-

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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 as indicated in comments:
B - John E. Bartmess
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

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Individual Reactions

C2HCl2O2- + Hydrogen cation = Acetic acid, dichloro-

By formula: C2HCl2O2- + H+ = C2H2Cl2O2

Quantity Value Units Method Reference Comment
Δr1374. ± 8.8kJ/molG+TSCaldwell, Renneboog, et al., 1989gas phase; B
Δr1374. ± 11.kJ/molG+TSCumming and Kebarle, 1978gas phase; B
Δr1369. ± 8.8kJ/molG+TSFujio, McIver, et al., 1981gas phase; value altered from reference due to change in acidity scale; B
Quantity Value Units Method Reference Comment
Δr1347. ± 8.4kJ/molIMRECaldwell, Renneboog, et al., 1989gas phase; B
Δr1347. ± 8.4kJ/molIMRECumming and Kebarle, 1978gas phase; B
Δr1342. ± 8.4kJ/molIMREFujio, McIver, et al., 1981gas phase; value altered from reference due to change in acidity scale; B

Water + Acetyl chloride, dichloro- = Hydrogen chloride + Acetic acid, dichloro-

By formula: H2O + C2HCl3O = HCl + C2H2Cl2O2

Quantity Value Units Method Reference Comment
Δr-107.7kJ/molCmPritchard and Skinner, 1950liquid phase; Heat of hydrolysis at 298 K; ALS

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

C2HCl2O2- + Hydrogen cation = Acetic acid, dichloro-

By formula: C2HCl2O2- + H+ = C2H2Cl2O2

Quantity Value Units Method Reference Comment
Δr1374. ± 8.8kJ/molG+TSCaldwell, Renneboog, et al., 1989gas phase
Δr1374. ± 11.kJ/molG+TSCumming and Kebarle, 1978gas phase
Δr1369. ± 8.8kJ/molG+TSFujio, McIver, et al., 1981gas phase; value altered from reference due to change in acidity scale
Quantity Value Units Method Reference Comment
Δr1347. ± 8.4kJ/molIMRECaldwell, Renneboog, et al., 1989gas phase
Δr1347. ± 8.4kJ/molIMRECumming and Kebarle, 1978gas phase
Δr1342. ± 8.4kJ/molIMREFujio, McIver, et al., 1981gas phase; value altered from reference due to change in acidity scale

References

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

Caldwell, Renneboog, et al., 1989
Caldwell, G.; Renneboog, R.; Kebarle, P., Gas Phase Acidities of Aliphatic Carboxylic Acids, Based on Measurements of Proton Transfer Equilibria, Can. J. Chem., 1989, 67, 4, 661, https://doi.org/10.1139/v89-092 . [all data]

Cumming and Kebarle, 1978
Cumming, J.B.; Kebarle, P., Summary of gas phase measurements involving acids AH. Entropy changes in proton transfer reactions involving negative ions. Bond dissociation energies D(A-H) and electron affinities EA(A), Can. J. Chem., 1978, 56, 1. [all data]

Fujio, McIver, et al., 1981
Fujio, M.; McIver, R.T., Jr.; Taft, R.W., Effects on the acidities of phenols from specific substituent-solvent interactions. Inherent substituent parameters from gas phase acidities, J. Am. Chem. Soc., 1981, 103, 4017. [all data]

Pritchard and Skinner, 1950
Pritchard, H.O.; Skinner, H.A., The heats of hydrolysis of the chloro-substituted acetyl chlorides, J. Chem. Soc., 1950, 272-276. [all data]


Notes

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