Selected ATcT [1, 2] enthalpy of formation based on version 1.122r of the Thermochemical Network [3]

This version of ATcT results was generated from an expansion of version 1.122q [4, 5] to include a non-rigid rotor anharmonic oscillator (NRRAO) partition function for hydroxymethyl [6], as well as data on 42 additional species, some of which are related to soot formation mechanisms.

Species Name Formula Image    ΔfH°(0 K)    ΔfH°(298.15 K) Uncertainty Units Relative
Molecular
Mass		 ATcT ID
Acetyl chlorideCH3C(O)Cl (l)CC(=O)Cl-272.13± 0.33kJ/mol78.4973 ±
0.0019		75-36-5*500

Top contributors to the provenance of ΔfH° of CH3C(O)Cl (l)

The 9 contributors listed below account for 80.5% of the provenance of ΔfH° of CH3C(O)Cl (l).

Please note: The list is limited to 20 most important contributors or, if less, a number sufficient to account for 90% of the provenance. The Reference acts as a further link to the relevant references and notes for the measurement. The Measured Quantity is normaly given in the original units; in cases where we have reinterpreted the original measurement, the listed value may differ from that given by the authors. The quoted uncertainty is the a priori uncertainty used as input when constructing the initial Thermochemical Network, and corresponds either to the value proposed by the original authors or to our estimate; if an additional multiplier is given in parentheses immediately after the prior uncertainty, it corresponds to the factor by which the prior uncertainty needed to be multiplied during the ATcT analysis in order to make that particular measurement consistent with the prevailing knowledge contained in the Thermochemical Network.

Contribution
(%)		TN
ID		 Reaction Measured Quantity Reference
37.74085.1 CH3C(O)Cl (l) + H2O (cr,l) → CH3C(O)OH (aq, 75 H2O) + HCl (aq, 75 H2O) ΔrH°(298.15 K) = -22.07 ± 0.07 kcal/molCarson 1949
10.94053.2 CH3C(O)OH (l) + 2 O2 (g) → 2 CO2 (g) + 2 H2O (cr,l) ΔrH°(298.15 K) = -209.125 ± 0.054 kcal/molLebedeva 1964
8.94086.1 CH3C(O)Cl (l) + H2O (cr,l) → CH3C(O)OH (aq, 1500 H2O) + HCl (aq, 1500 H2O) ΔrH°(298.15 K) = -22.22 ± 0.10 (×1.445) kcal/molPritchard 1950, Parker 1965, NBS Tables 1989
8.54063.3 CH3C(O)OH (l) → CH3C(O)OH (aq, 700 H2O) ΔrH°(298.15 K) = -0.293 ± 0.05 kcal/molParker 1965, est unc
4.84053.3 CH3C(O)OH (l) + 2 O2 (g) → 2 CO2 (g) + 2 H2O (cr,l) ΔrH°(298.15 K) = -875.14 ± 0.34 kJ/molSteele 1997
3.24053.1 CH3C(O)OH (l) + 2 O2 (g) → 2 CO2 (g) + 2 H2O (cr,l) ΔrH°(298.15 K) = -874.54 ± 0.30 (×1.384) kJ/molEvans 1959
2.34081.7 2 CH3C(O)Cl (g) + CH2O (g) → 2 CH3CHO (g) + CCl2O (g) ΔrH°(0 K) = 10.13 ± 0.9 kcal/molRuscic W1RO
2.14054.2 CH3C(O)OH (l) → CH3C(O)OH (aq) ΔrH°(298.15 K) = -0.360 ± 0.100 kcal/molParker 1965, NBS Tables 1989, est unc
1.84081.4 2 CH3C(O)Cl (g) + CH2O (g) → 2 CH3CHO (g) + CCl2O (g) ΔrH°(0 K) = 9.60 ± 1.0 kcal/molRuscic G4

Top 10 species with enthalpies of formation correlated to the ΔfH° of CH3C(O)Cl (l)

Please note: The correlation coefficients are obtained by renormalizing the off-diagonal elements of the covariance matrix by the corresponding variances.
The correlation coefficient is a number from -1 to 1, with 1 representing perfectly correlated species, -1 representing perfectly anti-correlated species, and 0 representing perfectly uncorrelated species.

Correlation
Coefficent
(%)		Species Name Formula Image    ΔfH°(0 K)    ΔfH°(298.15 K) Uncertainty Units Relative
Molecular
Mass		 ATcT ID
98.6 Acetyl chlorideCH3C(O)Cl (g)CC(=O)Cl-232.58-241.57± 0.33kJ/mol78.4973 ±
0.0019		75-36-5*0
63.0 Acetic acidCH3C(O)OH (aq, 75 H2O)CC(=O)O-484.69± 0.23kJ/mol60.0520 ±
0.0017		64-19-7*825
62.9 Acetic acidCH3C(O)OH (aq, 700 H2O)CC(=O)O-484.88± 0.23kJ/mol60.0520 ±
0.0017		64-19-7*835
62.9 Acetic acidCH3C(O)OH (aq)CC(=O)O-485.16± 0.23kJ/mol60.0520 ±
0.0017		64-19-7*800
62.9 Acetic acidCH3C(O)OH (aq, 1500 H2O)CC(=O)O-484.89± 0.23kJ/mol60.0520 ±
0.0017		64-19-7*840
62.9 Acetic acidCH3C(O)OH (aq, 1000 H2O)CC(=O)O-484.89± 0.23kJ/mol60.0520 ±
0.0017		64-19-7*839
62.9 Acetic acidCH3C(O)OH (aq, 500 H2O)CC(=O)O-484.87± 0.23kJ/mol60.0520 ±
0.0017		64-19-7*833
62.9 Acetic acidCH3C(O)OH (aq, 10000 H2O)CC(=O)O-484.92± 0.23kJ/mol60.0520 ±
0.0017		64-19-7*850
46.5 Acetic acidCH3C(O)OH (l)CC(=O)O-484.08-483.65± 0.18kJ/mol60.0520 ±
0.0017		64-19-7*500
12.5 AcetaldehydeCH3CHO (g)CC=O-155.06-165.54± 0.25kJ/mol44.0526 ±
0.0017		75-07-0*0

Most Influential reactions involving CH3C(O)Cl (l)

Please note: The list, which is based on a hat (projection) matrix analysis, is limited to no more than 20 largest influences.

Influence
Coefficient		 TN
ID		 Reaction Measured Quantity Reference
0.9254084.7 CH3C(O)Cl (l) → CH3C(O)Cl (g) ΔrG°(298.15 K) = 2.416 ± 0.055 kJ/molMcDonald 1959, 3rd Law
0.7224085.1 CH3C(O)Cl (l) + H2O (cr,l) → CH3C(O)OH (aq, 75 H2O) + HCl (aq, 75 H2O) ΔrH°(298.15 K) = -22.07 ± 0.07 kcal/molCarson 1949
0.1704086.1 CH3C(O)Cl (l) + H2O (cr,l) → CH3C(O)OH (aq, 1500 H2O) + HCl (aq, 1500 H2O) ΔrH°(298.15 K) = -22.22 ± 0.10 (×1.445) kcal/molPritchard 1950, Parker 1965, NBS Tables 1989
0.0304086.2 CH3C(O)Cl (l) + H2O (cr,l) → CH3C(O)OH (aq, 1500 H2O) + HCl (aq, 1500 H2O) ΔrH°(298.15 K) = -22.55 ± 0.34 kcal/molDevore 1969
0.0174084.2 CH3C(O)Cl (l) → CH3C(O)Cl (g) ΔrH°(298.15 K) = 30.29 ± 0.40 kJ/molNBS Tables 1989
0.0174084.3 CH3C(O)Cl (l) → CH3C(O)Cl (g) ΔrG°(298.15 K) = 2.19 ± 0.40 kJ/molNBS Tables 1989
0.0134084.8 CH3C(O)Cl (l) → CH3C(O)Cl (g) ΔrH°(298.15 K) = 31.02 ± 0.32 (×1.445) kJ/molMcDonald 1959, 2nd Law
0.0094084.1 CH3C(O)Cl (l) → CH3C(O)Cl (g) ΔrH°(298.15 K) = 30.03 ± 0.24 (×2.229) kJ/molThermoData 2004
0.0074084.5 CH3C(O)Cl (l) → CH3C(O)Cl (g) ΔrG°(298.15 K) = 0.43 ± 0.02 (×7.179) kcal/molDevore 1969, 3rd Law
0.0054084.4 CH3C(O)Cl (l) → CH3C(O)Cl (g) ΔrH°(298.15 K) = 7.13 ± 0.05 (×3.513) kcal/molMathews 1931, est unc
0.0004084.6 CH3C(O)Cl (l) → CH3C(O)Cl (g) ΔrH°(298.15 K) = 5.72 ± 0.07 (×23.12) kcal/molDevore 1969, 2nd Law
References
1   B. Ruscic, R. E. Pinzon, M. L. Morton, G. von Laszewski, S. Bittner, S. G. Nijsure, K. A. Amin, M. Minkoff, and A. F. Wagner,
Introduction to Active Thermochemical Tables: Several "Key" Enthalpies of Formation Revisited.
J. Phys. Chem. A 108, 9979-9997 (2004) [DOI: 10.1021/jp047912y]
2   B. Ruscic, R. E. Pinzon, G. von Laszewski, D. Kodeboyina, A. Burcat, D. Leahy, D. Montoya, and A. F. Wagner,
Active Thermochemical Tables: Thermochemistry for the 21st Century.
J. Phys. Conf. Ser. 16, 561-570 (2005) [DOI: 10.1088/1742-6596/16/1/078]
3   B. Ruscic and D. H. Bross,
Active Thermochemical Tables (ATcT) values based on ver. 1.122r of the Thermochemical Network, Argonne National Laboratory, Lemont, Illinois 2021 [DOI: 10.17038/CSE/1822363]; available at ATcT.anl.gov
4   D. Feller, D. H. Bross, and B. Ruscic,
Enthalpy of Formation of C2H2O4 (Oxalic Acid) from High-Level Calculations and the Active Thermochemical Tables Approach.
J. Phys. Chem. A 123, 3481-3496 (2019) [DOI: 10.1021/acs.jpca.8b12329]
5   B. K. Welch, R. Dawes, D. H. Bross, and B. Ruscic,
An Automated Thermochemistry Protocol Based on Explicitly Correlated Coupled-Cluster Theory: The Methyl and Ethyl Peroxy Families.
J. Phys. Chem. A 123, 5673-5682 (2019) [DOI: 10.1021/acs.jpca.8b12329]
6   D. H. Bross, H.-G. Yu, L. B. Harding, and B. Ruscic,
Active Thermochemical Tables: The Partition Function of Hydroxymethyl (CH2OH) Revisited.
J. Phys. Chem. A 123, 4212-4231 (2019) [DOI: 10.1021/acs.jpca.9b02295]
7   B. Ruscic,
Uncertainty Quantification in Thermochemistry, Benchmarking Electronic Structure Computations, and Active Thermochemical Tables.
Int. J. Quantum Chem. 114, 1097-1101 (2014) [DOI: 10.1002/qua.24605]
Formula The aggregate state is given in parentheses following the formula, such as: g - gas-phase, cr - crystal, l - liquid, etc.
Uncertainties The listed uncertainties correspond to estimated 95% confidence limits, as customary in thermochemistry (see, for example, Ruscic [7]).
Note that an uncertainty of ± 0.000 kJ/mol indicates that the estimated uncertainty is < ± 0.0005 kJ/mol.
Website Functionality Credits The reorganization of the website was developed and implemented by David H. Bross (ANL).
The find function is based on the complete Species Dictionary entries for the appropriate version of the ATcT TN.
The molecule images are rendered by Indigo-depict.
The XYZ renderings are based on Jmol: an open-source Java viewer for chemical structures in 3D. http://www.jmol.org/.
Acknowledgement This work was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences and Biosciences under Contract No. DE-AC02-06CH11357.