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endo-Dicyclopentadiene

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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

Benzene, 1-azido-4-nitro- + endo-Dicyclopentadiene = C16H16N4O2

By formula: C6H4N4O2 + C10H12 = C16H16N4O2

Quantity Value Units Method Reference Comment
Deltar-151.kJ/molCmSamuilov, Movchan, et al., 1985solid phase; solvent: Chlorobenzene

endo-Dicyclopentadiene + Benzene, azido- = C16H17N3

By formula: C10H12 + C6H5N3 = C16H17N3

Quantity Value Units Method Reference Comment
Deltar-161.kJ/molCmSamuilov, Movchan, et al., 1985solid phase; solvent: Chlorobenzene

21,3-Cyclopentadiene = endo-Dicyclopentadiene

By formula: 2C5H6 = C10H12

Quantity Value Units Method Reference Comment
Deltar-195.1kJ/molEqkLenz and Vaughan, 1989gas phase

References

Go To: Top, Reaction thermochemistry data, Notes

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

Samuilov, Movchan, et al., 1985
Samuilov, Ya.D.; Movchan, A.I.; Solov'eva, S.E.; Konovalov, A.I., Thermochemical and kinetic study of 1,3-dipolar cycloadditions involving aryl azides and nitrones, Zh. Org. Khim., 1985, 21, 1772-1776. [all data]

Lenz and Vaughan, 1989
Lenz, T.G.; Vaughan, J.D., Employing force-field calculations to predict equilibrium constants and other thermodynamic properties for the dimerization of 1,3-cyclopentadiene, J. Phys. Chem., 1989, 93, 1592-1596. [all data]


Notes

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