Biphenyl
- Formula: C12H10
- Molecular weight: 154.2078
- IUPAC Standard InChIKey: ZUOUZKKEUPVFJK-UHFFFAOYSA-N
- CAS Registry Number: 92-52-4
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Isotopologues:
- Other names: 1,1'-Biphenyl; Bibenzene; Diphenyl; Phenylbenzene; 1,1'-Diphenyl; Lemonene; Phenador-X; PhPh; Xenene; Carolid AL; Tetrosin LY; NSC 14916; 1,1-Biphenyl
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Enthalpy of combustion of solid at standard conditions (nominally 298.15 K, 1 atm.)
Go To: Top, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
ΔcH°solid (kJ/mol) | Method | Reference | Comment |
---|---|---|---|
-6248. ± 2. | Ccb | Montgomery, Rossini, et al., 1978 | Corresponding ΔfHºsolid = 96.73 kJ/mol (simple calculation by NIST; no Washburn corrections); ALS |
-6251.8 ± 1.4 | Ccb | Coleman and Pilcher, 1966 | Corresponding ΔfHºsolid = 100.5 kJ/mol (simple calculation by NIST; no Washburn corrections); ALS |
-6248.2 ± 4.0 | Ccb | Mackle and O'Hare, 1963 | Corresponding ΔfHºsolid = 96.90 kJ/mol (simple calculation by NIST; no Washburn corrections); ALS |
-6248.5 ± 1.6 | Ccb | Parks and Vaughan, 1951 | Reanalyzed by Cox and Pilcher, 1970, Original value = -6247.97 kJ/mol; Corresponding ΔfHºsolid = 97.24 kJ/mol (simple calculation by NIST; no Washburn corrections); ALS |
-6248.8 ± 6.3 | Ccb | Brull, 1935 | Reanalyzed by Cox and Pilcher, 1970, Original value = -6247.80 kJ/mol; Corresponding ΔfHºsolid = 97.53 kJ/mol (simple calculation by NIST; no Washburn corrections); ALS |
-6243. | Ccb | Wieland, Heymann, et al., 1934 | Corresponding ΔfHºsolid = 92. kJ/mol (simple calculation by NIST; no Washburn corrections); ALS |
-6276.0 | Ccb | Barker, 1925 | Author was aware that data differs from previously reported values; Corresponding ΔfHºsolid = 125. kJ/mol (simple calculation by NIST; no Washburn corrections); ALS |
References
Go To: Top, Enthalpy of combustion of solid at standard conditions (nominally 298.15 K, 1 atm.), Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Montgomery, Rossini, et al., 1978
Montgomery, R.L.; Rossini, F.D.; Mansson, M.,
Enthalpies of combustion, vaporization, and formation of phenylbenzene, cyclohexylbenzene, and cyclohexylcyclohexane; enthalpy of hydrogenation of certain aromatic systems,
J. Chem. Eng. Data, 1978, 23, 125-129. [all data]
Coleman and Pilcher, 1966
Coleman, D.J.; Pilcher, G.,
Heats of combustion of biphenyl, bibenzyl, naphthalene, anthracene, and phenanthrene,
Trans. Faraday Soc., 1966, 62, 821-827. [all data]
Mackle and O'Hare, 1963
Mackle, H.; O'Hare, P.A.G.,
A high-precision aneroid semi-micro combustion calorimeter,
Trans. Faraday Soc., 1963, 59, 2693-2701. [all data]
Parks and Vaughan, 1951
Parks, G.S.; Vaughan, L.M.,
The heat of combustion of biphenyl,
J. Am. Chem. Soc., 1951, 73, 2380-2381. [all data]
Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G.,
Thermochemistry of Organic and Organometallic Compounds, Academic Press, New York, 1970, 1-636. [all data]
Brull, 1935
Brull, L.,
Sui calori di combustione di alcuni derivati del bifenil,
Gazz. Chim. Ital., 1935, 65, 19-28. [all data]
Wieland, Heymann, et al., 1934
Wieland, H.; Heymann, K.; Tsatsas, T.; Juchum, D.; Varvoglis, G.; Labriola, G.; Dobbelstein, O.; Boyd-Barrett, H.S.,
Uber das Auftreten freier Radikale bei chemischen Reaktionen. VIII,
Ann., 1934, 514, 145-181. [all data]
Barker, 1925
Barker, M.F.,
Calorific value and constitution,
J. Phys. Chem., 1925, 29, 1345-1363. [all data]
Notes
Go To: Top, Enthalpy of combustion of solid at standard conditions (nominally 298.15 K, 1 atm.), References
- Symbols used in this document:
ΔcH°solid Enthalpy of combustion of solid at standard conditions - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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