1,3-Dioxane, 4,6-dimethyl-, cis-

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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
Δfliquid-474.8 ± 2.4kJ/molCcbPihlaja and Luoma, 1968 
Quantity Value Units Method Reference Comment
Δcliquid-3601.3 ± 2.4kJ/molCcbPihlaja and Luoma, 1968Corresponding Δfliquid = -474.80 kJ/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 by: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

Quantity Value Units Method Reference Comment
Tboil388.15KN/AEliel and Knoeber, 1968Uncertainty assigned by TRC = 1.5 K

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:


Gas phase ion energetics 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: Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

Appearance energy determinations

Ion AE (eV) Other Products MethodReferenceComment
C6H11O2+9.693 ± 0.005HEIPihlaja and Jalonen, 1971 

References

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

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

Pihlaja and Luoma, 1968
Pihlaja, K.; Luoma, S., Heats of formation and conformational energies of 1,3-dioxane and its methyl homologues, Acta Chem. Scand., 1968, 22, 2401-2414. [all data]

Eliel and Knoeber, 1968
Eliel, E.L.; Knoeber, M.C., Conformational Analysis XVI. 1,3-Dioxanes, J. Am. Chem. Soc., 1968, 90, 3444. [all data]

Pihlaja and Jalonen, 1971
Pihlaja, K.; Jalonen, J., Appearance potentials determined by the electron-impact method as an analytical aid in the evaluation of conformational energies and clarification of ring conformation-I: Appearance potentials of the [M-R]+ ions formed in the primary fragmentation of stereoisomeric 1,3-dioxans. A direct route to conformational energies, Org. Mass Spectrom., 1971, 5, 1363. [all data]


Notes

Go To: Top, Condensed phase thermochemistry data, Phase change data, Gas phase ion energetics data, References