cis-octahydronaphthalene-2(1H)-one


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
Δcliquid-5867.2kJ/molCcbHuckel and Mentzel, 1926Corresponding Δfliquid = -354. kJ/mol (simple calculation by NIST; no Washburn corrections)
Δcliquid-5862.7 ± 4.5kJ/molCcbRoth and Lasse, 1925Corresponding Δfliquid = -359.1 kJ/mol (simple calculation by NIST; no Washburn corrections)

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

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Individual Reactions

2(1H)-Naphthalenone, octahydro-, trans- = cis-octahydronaphthalene-2(1H)-one

By formula: C10H16O = C10H16O

Quantity Value Units Method Reference Comment
Δr10.5 ± 1.3kJ/molEqkAllinger and Siefert, 1972liquid phase; At 488 K

References

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

Huckel and Mentzel, 1926
Huckel, W.; Mentzel, R., Zur Stereochemie bicyclischer Ringsteme II. Die Stereoisomerie des Dekahydronaphtalins und seiner Derivate II. Stereoisomere β-substituierte Dekaline, Ann., 1926, 451, 109-132. [all data]

Roth and Lasse, 1925
Roth, W.A.; Lasse, R., Verbrennungswarme der Dekahydro-naphthaline und der Dekalone, Ann., 1925, 441, 48-53. [all data]

Allinger and Siefert, 1972
Allinger, N.L.; Siefert, J.H., Conformational analysis. LXXXVI. The equilibrium between the cis and trans isomers of 2-decalone, J. Am. Chem. Soc., 1972, 94, 8082-8084. [all data]


Notes

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