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

This version of ATcT results was generated from an expansion of version 1.122e [4] to include results centered on the determination of the appearance energy of CH3+ from CH4. [5].

Species Name Formula Image    ΔfH°(0 K)    ΔfH°(298.15 K) Uncertainty Units Relative
Molecular
Mass		 ATcT ID
Vinyl chlorideCH2CHCl (g)C=CCl29.2621.67± 0.30kJ/mol62.4979 ±
0.0018		75-01-4*0

Representative Geometry of CH2CHCl (g)

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Top contributors to the provenance of ΔfH° of CH2CHCl (g)

The 20 contributors listed below account only for 73.5% of the provenance of ΔfH° of CH2CHCl (g).
A total of 110 contributors would be needed to account for 90% of the provenance.

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
15.24247.8 CH2CHCl (g) → 2 C (g) + 3 H (g) + Cl (g) ΔrH°(0 K) = 2161.08 ± 0.70 kJ/molHarding 2007
14.34254.2 HCCH (g) + HCl (g) → CH2CHCl (g) ΔrH°(0 K) = -107.17 ± 0.70 kJ/molHarding 2007
13.84251.1 CH2CHCl (g) + H (g) → CH2CH2 (g) + Cl (g) ΔrH°(0 K) = -65.15 ± 0.70 kJ/molHarding 2007
13.74250.7 CH2CHCl (g) + H2 (g) → CH2CH2 (g) + HCl (g) ΔrH°(0 K) = -60.54 ± 0.70 kJ/molHarding 2007
2.04252.1 CH2CHCl (g) → [CH2CH]+ (g) + Cl (g) ΔrH°(0 K) = 12.530 ± 0.010 eVShuman 2008
1.84255.2 CH3CHCl2 (g) → CH2CHCl (g) + HCl (g) ΔrG°(420.5 K) = 0.8 ± 0.7 kJ/molLevanova 1976, Manion 2002, 3rd Law
1.74266.4 CHClCHCl (g, cis) + CH2CH2 (g) → 2 CH2CHCl (g) ΔrH°(0 K) = -1.95 ± 0.85 kcal/molRuscic W1RO
1.54266.1 CHClCHCl (g, cis) + CH2CH2 (g) → 2 CH2CHCl (g) ΔrH°(0 K) = -1.71 ± 0.90 kcal/molRuscic G3X
1.54266.2 CHClCHCl (g, cis) + CH2CH2 (g) → 2 CH2CHCl (g) ΔrH°(0 K) = -1.66 ± 0.90 kcal/molRuscic G4
1.34258.1 CH3CHCl2 (cr,l) → CH2CHCl (g) + HCl (g) ΔrH°(308 K) = 93.24 ± 0.7 kJ/molLevanova 1976, Manion 2002, 2nd Law
1.24266.3 CHClCHCl (g, cis) + CH2CH2 (g) → 2 CH2CHCl (g) ΔrH°(0 K) = -1.64 ± 1.00 kcal/molRuscic CBS-n
0.72032.1 CH2CH2 (g) + 3 O2 (g) → 2 CO2 (g) + 2 H2O (cr,l) ΔrH°(298.15 K) = -1411.18 ± 0.30 kJ/molRossini 1937
0.54204.4 CH3CCl3 (g) + CH3CH2Cl (g) → 2 CH3CHCl2 (g) ΔrH°(0 K) = -3.18 ± 0.9 (×1.044) kcal/molRuscic W1RO
0.5118.2 1/2 O2 (g) + H2 (g) → H2O (cr,l) ΔrH°(298.15 K) = -285.8261 ± 0.040 kJ/molRossini 1939, Rossini 1931, Rossini 1931b, note H2Oa, Rossini 1930
0.54206.2 CH3CCl3 (l) + 2 O2 (g) → 2 CO2 (g) + 3 HCl (aq, 600 H2O) ΔrH°(298.15 K) = -264.83 ± 0.19 kcal/molHu 1972
0.54248.6 CH2CHCl (g) + CH4 (g) → CH2CH2 (g) + CH3Cl (g) ΔrH°(0 K) = 5.39 ± 0.85 kcal/molRuscic W1RO
0.54252.3 CH2CHCl (g) → [CH2CH]+ (g) + Cl (g) ΔrH°(0 K) = 12.538 ± 0.02 eVSheng 1995
0.44204.2 CH3CCl3 (g) + CH3CH2Cl (g) → 2 CH3CHCl2 (g) ΔrH°(0 K) = -2.28 ± 1.0 kcal/molRuscic G4
0.44249.4 CH2CHCl (g) + CH3CH3 (g) → CH2CH2 (g) + CH3CH2Cl (g) ΔrH°(0 K) = 0.58 ± 0.85 kcal/molRuscic W1RO
0.44255.1 CH3CHCl2 (g) → CH2CHCl (g) + HCl (g) ΔrH°(403 K) = 61.7 ± 1.0 (×1.384) kJ/molLevanova 1976, Manion 2002, 2nd Law

Top 10 species with enthalpies of formation correlated to the ΔfH° of CH2CHCl (g)

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
45.6 1,1-DichloroethaneCH3CHCl2 (g)CC(Cl)Cl-120.33-133.11± 0.44kJ/mol98.9586 ±
0.0024		75-34-3*0
44.5 1,1-DichloroethaneCH3CHCl2 (cr,l)CC(Cl)Cl-163.91± 0.48kJ/mol98.9586 ±
0.0024		75-34-3*500
28.6 EthyleneCH2CH2 (g)C=C60.8852.36± 0.12kJ/mol28.0532 ±
0.0016		74-85-1*0
28.6 Ethylene cation[CH2CH2]+ (g)C=[CH2+]1075.201067.98± 0.12kJ/mol28.0526 ±
0.0016		34470-02-5*0
27.5 Vinylium[CH2CH]+ (g)[CH+]1[CH][H]11118.941115.50± 0.57kJ/mol27.0447 ±
0.0016		14604-48-9*0
26.8 Vinyl bromideCH2CHBr (g)C=CBr88.5673.76± 0.58kJ/mol106.9492 ±
0.0019		593-60-2*0
22.2 AcetyleneHCCH (g)C#C228.82228.26± 0.13kJ/mol26.0373 ±
0.0016		74-86-2*0
22.2 Acetylene cation[HCCH]+ (g)C#[CH+]1328.831328.17± 0.13kJ/mol26.0367 ±
0.0016		25641-79-6*0
21.6 Carbon atomC (g)[C]711.399716.884± 0.047kJ/mol12.01070 ±
0.00080		7440-44-0*0
21.6 Carbon atomC (g, triplet)[C]711.399716.884± 0.047kJ/mol12.01070 ±
0.00080		7440-44-0*1

Most Influential reactions involving CH2CHCl (g)

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
1.0004261.1 (NNC)ClCH3 (g) → CH2CHCl (g) + N2 (g) ΔrH°(298.15 K) = -46.9 ± 9.5 kcal/molArcher 1976, as quoted by Pedley 1986
0.3904258.1 CH3CHCl2 (cr,l) → CH2CHCl (g) + HCl (g) ΔrH°(308 K) = 93.24 ± 0.7 kJ/molLevanova 1976, Manion 2002, 2nd Law
0.3384252.1 CH2CHCl (g) → [CH2CH]+ (g) + Cl (g) ΔrH°(0 K) = 12.530 ± 0.010 eVShuman 2008
0.3244255.2 CH3CHCl2 (g) → CH2CHCl (g) + HCl (g) ΔrG°(420.5 K) = 0.8 ± 0.7 kJ/molLevanova 1976, Manion 2002, 3rd Law
0.1754254.2 HCCH (g) + HCl (g) → CH2CHCl (g) ΔrH°(0 K) = -107.17 ± 0.70 kJ/molHarding 2007
0.1704247.8 CH2CHCl (g) → 2 C (g) + 3 H (g) + Cl (g) ΔrH°(0 K) = 2161.08 ± 0.70 kJ/molHarding 2007
0.1644250.7 CH2CHCl (g) + H2 (g) → CH2CH2 (g) + HCl (g) ΔrH°(0 K) = -60.54 ± 0.70 kJ/molHarding 2007
0.1644251.1 CH2CHCl (g) + H (g) → CH2CH2 (g) + Cl (g) ΔrH°(0 K) = -65.15 ± 0.70 kJ/molHarding 2007
0.1554276.4 CHClCCl2 (g) + CH2CH2 (g) → CH2CHCl (g) + CH2CCl2 (g) ΔrH°(0 K) = -3.23 ± 0.85 kcal/molRuscic W1RO
0.1384276.1 CHClCCl2 (g) + CH2CH2 (g) → CH2CHCl (g) + CH2CCl2 (g) ΔrH°(0 K) = -2.80 ± 0.90 kcal/molRuscic G3X
0.1384276.2 CHClCCl2 (g) + CH2CH2 (g) → CH2CHCl (g) + CH2CCl2 (g) ΔrH°(0 K) = -2.74 ± 0.90 kcal/molRuscic G4
0.1124276.3 CHClCCl2 (g) + CH2CH2 (g) → CH2CHCl (g) + CH2CCl2 (g) ΔrH°(0 K) = -2.73 ± 1.00 kcal/molRuscic CBS-n
0.0844252.3 CH2CHCl (g) → [CH2CH]+ (g) + Cl (g) ΔrH°(0 K) = 12.538 ± 0.02 eVSheng 1995
0.0834255.1 CH3CHCl2 (g) → CH2CHCl (g) + HCl (g) ΔrH°(403 K) = 61.7 ± 1.0 (×1.384) kJ/molLevanova 1976, Manion 2002, 2nd Law
0.0704267.4 CHClCHCl (g, cis) + CH2 (g, singlet) → CH2CHCl (g) + CHCl (g, singlet) ΔrH°(0 K) = -20.26 ± 0.90 kcal/molRuscic W1RO
0.0574267.2 CHClCHCl (g, cis) + CH2 (g, singlet) → CH2CHCl (g) + CHCl (g, singlet) ΔrH°(0 K) = -19.91 ± 1.00 kcal/molRuscic G4
0.0474267.1 CHClCHCl (g, cis) + CH2 (g, singlet) → CH2CHCl (g) + CHCl (g, singlet) ΔrH°(0 K) = -19.91 ± 1.10 kcal/molRuscic G3X
0.0414266.4 CHClCHCl (g, cis) + CH2CH2 (g) → 2 CH2CHCl (g) ΔrH°(0 K) = -1.95 ± 0.85 kcal/molRuscic W1RO
0.0364266.2 CHClCHCl (g, cis) + CH2CH2 (g) → 2 CH2CHCl (g) ΔrH°(0 K) = -1.66 ± 0.90 kcal/molRuscic G4
0.0364266.1 CHClCHCl (g, cis) + CH2CH2 (g) → 2 CH2CHCl (g) ΔrH°(0 K) = -1.71 ± 0.90 kcal/molRuscic G3X
References (for your convenience, also available in RIS and BibTex format)
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. 1.122g of the Thermochemical Network (2019); available at ATcT.anl.gov
4   J. P. Porterfield, D. H. Bross, B. Ruscic, J. H. Thorpe, T. L. Nguyen, J. H. Baraban, J. F. Stanton, J. W. Daily, and G. B. Ellison,
Thermal Decomposition of Potential Ester Biofuels, Part I: Methyl Acetate and Methyl Butanoate.
J. Chem. Phys. A 121, 4658-4677 (2017) [DOI: 10.1021/acs.jpca.7b02639] (Veronica Vaida Festschrift)
5   Y.-C. Chang, B. Xiong, D. H. Bross, B. Ruscic, and C. Y. Ng,
A Vacuum Ultraviolet laser Pulsed Field Ionization-Photoion Study of Methane (CH4): Determination of the Appearance Energy of Methylium From Methane with Unprecedented Precision and the Resulting Impact on the Bond Dissociation Energies of CH4 and CH4+.
Phys. Chem. Chem. Phys. 19, 9592-9605 (2017) [DOI: 10.1039/c6cp08200a] (part of 2017 PCCP Hot Articles collection)
6   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 [6]).
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.