Benzene, cyclopropyl-

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Gas phase 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:
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DRB - Donald R. Burgess, Jr.

Quantity Value Units Method Reference Comment
Δfgas36.02 ± 0.24kcal/molCcbFuchs, Hallman, et al., 1982Heat of combustion is not reported; ALS
Δfgas35.9 ± 0.2kcal/molN/AKozina, Lukina, et al., 1961Value computed using ΔfHliquid° value of 100.2±0.8 kj/mol from Kozina, Lukina, et al., 1961 and ΔvapH° value of 50.2±0.1 kj/mol from missing citation.; DRB

Condensed phase 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 by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Quantity Value Units Method Reference Comment
Δfliquid24.0 ± 0.2kcal/molCcbKozina, Lukina, et al., 1961Error in hf by author
Quantity Value Units Method Reference Comment
Δcliquid-1213.3kcal/molCcbFierens and Nasielski, 1962Corresponding Δfliquid = 25.3 kcal/mol (simple calculation by NIST; no Washburn corrections)
Δcliquid-1212.0 ± 0.2kcal/molCcbKozina, Lukina, et al., 1961Error in hf by author; Corresponding Δfliquid = 24.0 kcal/mol (simple calculation by NIST; no Washburn corrections)

Phase change 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:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
BS - Robert L. Brown and Stephen E. Stein
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Quantity Value Units Method Reference Comment
Tboil444.KN/AHahn, Corbin, et al., 1968Uncertainty assigned by TRC = 4. K; TRC
Tboil438.KN/AGragson, Greenlee, et al., 1955Uncertainty assigned by TRC = 3. K; TRC
Tboil443.65KN/ALespieau, 1930Uncertainty assigned by TRC = 2. K; compound identified as "phenyltrimethylene"; TRC
Quantity Value Units Method Reference Comment
Δvap12.00kcal/molN/AMajer and Svoboda, 1985 
Δvap12.00 ± 0.02kcal/molVFuchs, Hallman, et al., 1982Heat of combustion is not reported; ALS

Reduced pressure boiling point

Tboil (K) Pressure (atm) Reference Comment
446.80.991Aldrich Chemical Company Inc., 1990BS
353.20.049Weast and Grasselli, 1989BS

In addition to the Thermodynamics Research Center (TRC) data available from this site, much more physical and chemical property data is available from the following TRC products:


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 by: John E. Bartmess

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.

Individual Reactions

C9H9- + Hydrogen cation = Benzene, cyclopropyl-

By formula: C9H9- + H+ = C9H10

Quantity Value Units Method Reference Comment
Δr389.8 ± 3.1kcal/molG+TSChou, Dahlke, et al., 1993gas phase; Between water, furan
Quantity Value Units Method Reference Comment
Δr382.1 ± 3.0kcal/molIMRBChou, Dahlke, et al., 1993gas phase; Between water, furan
Δr384.0 ± 3.0kcal/molIMRBAndrist, DePuy, et al., 1984gas phase

References

Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Notes

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

Fuchs, Hallman, et al., 1982
Fuchs, R.; Hallman, J.H.; Perlman, M.O., Thermochemistry of conjugation of simple cyclopropane derivatives, Can. J. Chem., 1982, 60, 1832-1835. [all data]

Kozina, Lukina, et al., 1961
Kozina, M.P.; Lukina, M.Yu.; Zubareya, N.D.; Safonova, I.L.; Skuratov, S.M.; Kazansky, B.A., The energy of combustion of some phenylcyclopropanes, Dokl. Akad. Nauk SSSR, 1961, 138, 843-845. [all data]

Fierens and Nasielski, 1962
Fierens, P.J.C.; Nasielski, J., Chaleurs de combustion de derives cyclopropaniques et pouvoir de conjugaison du groupe cyclopropyle, Bull. Soc. Chim. Belg., 1962, 71, 187-202. [all data]

Hahn, Corbin, et al., 1968
Hahn, R.C.; Corbin, T.F.; Shechter, H., Electrical Effects of Cycloalkyl Groups, J. Am. Chem. Soc., 1968, 90, 3404-15. [all data]

Gragson, Greenlee, et al., 1955
Gragson, J.T.; Greenlee, K.W.; Derfer, J.M.; Boord, C.E., Cyclopropane Hydrocarbons from γ-Bromo Ethers, J. Org. Chem., 1955, 20, 275. [all data]

Lespieau, 1930
Lespieau, R., Phenyltrimethylene, C. R. Hebd. Seances Acad. Sci., 1930, 190, 1129-31. [all data]

Majer and Svoboda, 1985
Majer, V.; Svoboda, V., Enthalpies of Vaporization of Organic Compounds: A Critical Review and Data Compilation, Blackwell Scientific Publications, Oxford, 1985, 300. [all data]

Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc., Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]

Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]

Chou, Dahlke, et al., 1993
Chou, P.K.; Dahlke, G.D.; Kass, S.R., Unimolecular Rearrangements of Carbanions in the Gas Phase .2. Cyclopropyl Anions, J. Chem. Soc. Chem. Comm., 1993, 115, 1, 315, https://doi.org/10.1021/ja00054a045 . [all data]

Andrist, DePuy, et al., 1984
Andrist, A.H.; DePuy, C.H.; Squires, R.R., Structures of ssomeric anions in the gas phase: Arylallyl and arylcyclopropyl anions, J. Am. Chem. Soc., 1984, 106, 845. [all data]


Notes

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