Selected ATcT [1, 2] enthalpy of formation based on version 1.202 of the Thermochemical Network [3]

This version of ATcT results[3] was generated by additional expansion of version 1.176 in order to include species related to the thermochemistry of glycine[4].

Nitroethane

Formula: CH3CH2N(O)O (cr,l)

CAS RN: 79-24-3

ATcT ID: 79-24-3*500

SMILES: CC[N+](=O)[O-]

InChI: InChI=1S/C2H5NO2/c1-2-3(4)5/h2H2,1H3

InChIKey: MCSAJNNLRCFZED-UHFFFAOYSA-N

Hills Formula: C2H5N1O2

2D Image:

Aliases: CH3CH2N(O)O; Nitroethane

Relative Molecular Mass: 75.0666 ± 0.0017

Δ_fH°(0 K)	Δ_fH°(298.15 K)	Uncertainty	Units
-141.89	-144.10	± 0.57	kJ/mol

Top contributors to the provenance of Δ_fH° of CH3CH2N(O)O (cr,l)

The 17 contributors listed below account for 90.6% of the provenance of Δ_fH° of CH3CH2N(O)O (cr,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
44.0	7632.4	2 CH3CH2N(O)O (cr,l) + 9/2 O2 (g) → 4 CO2 (g) + 5 H2O (cr,l) + N2 (g)	Δ_rH°(298.15 K) = -649.0 ± 0.4 kcal/mol	Lebedeva 1973, note unc2
28.1	7632.1	2 CH3CH2N(O)O (cr,l) + 9/2 O2 (g) → 4 CO2 (g) + 5 H2O (cr,l) + N2 (g)	Δ_rH°(298.15 K) = -649.11 ± 0.50 kcal/mol	Prosen 1954, Cass 1958
3.4	7634.1	CH3CH2N(O)O (cr,l) → CH3CH2N(O)O (g)	Δ_rH°(298.15 K) = 9.94 ± 0.10 kcal/mol	Holcomb 1949
1.7	7632.3	2 CH3CH2N(O)O (cr,l) + 9/2 O2 (g) → 4 CO2 (g) + 5 H2O (cr,l) + N2 (g)	Δ_rH°(298.15 K) = -650.83 ± 0.60 (×3.364) kcal/mol	Holcomb 1949
1.2	7630.5	CH3CH2N(O)O (g) + CH3OH (g) → CH3N(O)O (g) + CH3CH2OH (g)	Δ_rH°(0 K) = -0.74 ± 0.85 kcal/mol	Ruscic W1RO
1.1	7631.5	CH3CH2N(O)O (g) + CH3NH2 (g) → CH3N(O)O (g) + CH3CH2NH2 (g)	Δ_rH°(0 K) = 0.43 ± 0.85 kcal/mol	Ruscic W1RO
1.1	7630.2	CH3CH2N(O)O (g) + CH3OH (g) → CH3N(O)O (g) + CH3CH2OH (g)	Δ_rH°(0 K) = -0.76 ± 0.90 kcal/mol	Ruscic G4
1.1	7630.4	CH3CH2N(O)O (g) + CH3OH (g) → CH3N(O)O (g) + CH3CH2OH (g)	Δ_rH°(0 K) = -0.70 ± 0.90 kcal/mol	Ruscic CBS-n
1.1	7630.1	CH3CH2N(O)O (g) + CH3OH (g) → CH3N(O)O (g) + CH3CH2OH (g)	Δ_rH°(0 K) = -0.75 ± 0.90 kcal/mol	Ruscic G3X
1.0	7631.2	CH3CH2N(O)O (g) + CH3NH2 (g) → CH3N(O)O (g) + CH3CH2NH2 (g)	Δ_rH°(0 K) = 0.39 ± 0.90 kcal/mol	Ruscic G4
1.0	7631.4	CH3CH2N(O)O (g) + CH3NH2 (g) → CH3N(O)O (g) + CH3CH2NH2 (g)	Δ_rH°(0 K) = 0.52 ± 0.90 kcal/mol	Ruscic CBS-n
1.0	7631.1	CH3CH2N(O)O (g) + CH3NH2 (g) → CH3N(O)O (g) + CH3CH2NH2 (g)	Δ_rH°(0 K) = 0.52 ± 0.90 kcal/mol	Ruscic G3X
0.9	7596.1	2 CH3N(O)O (cr,l) + 3/2 O2 (g) → 2 CO2 (g) + 3 H2O (l) + N2 (g)	Δ_rH°(298.15 K) = -339.02 ± 0.28 kcal/mol	Prosen 1954, Cass 1958
0.9	7630.3	CH3CH2N(O)O (g) + CH3OH (g) → CH3N(O)O (g) + CH3CH2OH (g)	Δ_rH°(0 K) = -0.67 ± 1.00 kcal/mol	Ruscic CBS-n
0.8	7631.3	CH3CH2N(O)O (g) + CH3NH2 (g) → CH3N(O)O (g) + CH3CH2NH2 (g)	Δ_rH°(0 K) = 0.54 ± 1.00 kcal/mol	Ruscic CBS-n
0.8	7629.5	CH3CH2N(O)O (g) + CH3ONO (g, cis) → CH3N(O)O (g) + CH3CH2ONO (g, trans-cis)	Δ_rH°(0 K) = -0.42 ± 0.85 kcal/mol	Ruscic W1RO
0.7	7629.1	CH3CH2N(O)O (g) + CH3ONO (g, cis) → CH3N(O)O (g) + CH3CH2ONO (g, trans-cis)	Δ_rH°(0 K) = -0.53 ± 0.90 kcal/mol	Ruscic G3X

Top 10 species with enthalpies of formation correlated to the Δ_fH° of CH3CH2N(O)O (cr,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	Δ_fH°(0 K)	Δ_fH°(298.15 K)	Uncertainty	Units	Relative Molecular Mass	ATcT ID
78.0	Nitroethane	CH3CH2N(O)O (g)	-83.42	-102.75	± 0.62	kJ/mol	75.0666 ± 0.0017	79-24-3*0
17.7	Nitromethane	CH3N(O)O (g)	-60.58	-74.48	± 0.40	kJ/mol	61.0401 ± 0.0010	75-52-5*0
15.9	Nitromethane	CH3N(O)O (cr,l)	-113.95	-112.76	± 0.39	kJ/mol	61.0401 ± 0.0010	75-52-5*500
14.0	Ethyl nitrite	CH3CH2ONO (g, trans-cis)	-79.93	-98.67	± 0.86	kJ/mol	75.0666 ± 0.0017	109-95-5*1
14.0	Ethyl nitrite	CH3CH2ONO (g)	-79.93	-97.33	± 0.86	kJ/mol	75.0666 ± 0.0017	109-95-5*0
10.2	Propyl nitrite	CH3CH2CH2ONO (g)	-94.5	-118.3	± 1.7	kJ/mol	89.0932 ± 0.0025	543-67-9*0
10.2	Propyl nitrite	CH3CH2CH2ONO (g, gauche-trans-cis)	-94.5	-119.4	± 1.7	kJ/mol	89.0932 ± 0.0025	543-67-9*1
9.6	Carbonic acid	C(O)(OH)2 (aq, undissoc)		-698.669	± 0.028	kJ/mol	62.0248 ± 0.0012	463-79-6*1000
9.2	Water	H2O (cr,l)	-286.273	-285.801	± 0.022	kJ/mol	18.01528 ± 0.00033	7732-18-5*500
9.2	Water	H2O (l)		-285.801	± 0.022	kJ/mol	18.01528 ± 0.00033	7732-18-5*590

Most Influential reactions involving CH3CH2N(O)O (cr,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
0.893	7634.1	CH3CH2N(O)O (cr,l) → CH3CH2N(O)O (g)	Δ_rH°(298.15 K) = 9.94 ± 0.10 kcal/mol	Holcomb 1949
0.445	7632.4	2 CH3CH2N(O)O (cr,l) + 9/2 O2 (g) → 4 CO2 (g) + 5 H2O (cr,l) + N2 (g)	Δ_rH°(298.15 K) = -649.0 ± 0.4 kcal/mol	Lebedeva 1973, note unc2
0.284	7632.1	2 CH3CH2N(O)O (cr,l) + 9/2 O2 (g) → 4 CO2 (g) + 5 H2O (cr,l) + N2 (g)	Δ_rH°(298.15 K) = -649.11 ± 0.50 kcal/mol	Prosen 1954, Cass 1958
0.017	7632.3	2 CH3CH2N(O)O (cr,l) + 9/2 O2 (g) → 4 CO2 (g) + 5 H2O (cr,l) + N2 (g)	Δ_rH°(298.15 K) = -650.83 ± 0.60 (×3.364) kcal/mol	Holcomb 1949
0.003	7632.2	2 CH3CH2N(O)O (cr,l) + 9/2 O2 (g) → 4 CO2 (g) + 5 H2O (cr,l) + N2 (g)	Δ_rH°(298.15 K) = -653.2 ± 0.6 (×7.336) kcal/mol	Cass 1958
0.001	7634.2	CH3CH2N(O)O (cr,l) → CH3CH2N(O)O (g)	Δ_rH°(298.15 K) = 40.14 ± 11 kJ/mol	Stull 1947, 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 21^st 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. 1.202 of the Thermochemical Network (2024); available at ATcT.anl.gov
4		B. Ruscic and D. H. Bross Accurate and Reliable Thermochemistry by Data Analysis of Complex Thermochemical Networks using Active Thermochemical Tables: The Case of Glycine Thermochemistry Faraday Discuss. (in press) (2024) [DOI: 10.1039/D4FD00110A]
5		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]
6		B. Ruscic and D. H. Bross, Thermochemistry Computer Aided Chem. Eng. 45, 3-114 (2019) [DOI: 10.1016/B978-0-444-64087-1.00001-2]

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 [5] and Ruscic and Bross[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.