Naphthalene, 1,2,3,4-tetrahydro-1-methyl-

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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
Δcliquid-1498.6kcal/molCcbKaro, McLaughlin, et al., 1953Corrected from net heat of combustion; Corresponding Δfliquid = -14.2 kcal/mol (simple calculation by NIST; no Washburn corrections)
Δcliquid-1496.6kcal/molCcbHock and Knauel, 1951Corresponding Δfliquid = -16.2 kcal/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

Naphthalene, 1,2,3,4-tetrahydro-1-methyl- = Naphthalene, 1,2,3,4-tetrahydro-5-methyl-

By formula: C11H14 = C11H14

Quantity Value Units Method Reference Comment
Δr-1.7kcal/molEqkNieuwstad, Klapwijk, et al., 1973liquid phase

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.

Karo, McLaughlin, et al., 1953
Karo, W.; McLaughlin, R.L.; Hipsher, H.F., Dicyclic hydrocarbons. VI. 1,2,3,4-Tetrahydronaphthalene and 1-alkyl-1,2,3,4-tetrahydronaphthalenes, J. Am. Chem. Soc., 1953, 75, 3233-3235. [all data]

Hock and Knauel, 1951
Hock, I.H.; Knauel, G., Autoxydation von kohlenwasserstoffen, XIV. Mitteil. Uber die energetische stellung organischer hydroperoxyde, Chem. Ber., 1951, 84, 1-5. [all data]

Nieuwstad, Klapwijk, et al., 1973
Nieuwstad, Th.J.; Klapwijk, P.; Van Bekkum, H., Hydrogenation of alkyl-substituted naphthalenes over palladium, J. Catal., 1973, 29, 404-411. [all data]


Notes

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