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Polycyclische Aromaten pp 143–157Cite as

Die Chemische Reaktivität Polycyclischer Aromaten

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Zusammenfassung

Elektrophile Substitutionsreaktionen verlaufen bei PAHs mit erheblich größeren Geschwindigkeiten als beim Benzol und lassen sich unter milderen Reaktionsbedingungen durchführen. Das gilt auch für die Mehrfachsubstitution, und ist in der verglichen mit Benzol stärkeren Nucleophilie der PAHs begründet 1,2).

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Authors and Affiliations

  1. Castrop-Rauxel, Deutschland

    Prof. Dr. rer. nat. Maximilian Zander

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  1. Prof. Dr. rer. nat. Maximilian Zander
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© 1995 B. G. Teubner Stuttgart

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Zander, M. (1995). Die Chemische Reaktivität Polycyclischer Aromaten. In: Polycyclische Aromaten. Teubner Studienbücher Chemie. Vieweg+Teubner Verlag. https://doi.org/10.1007/978-3-322-96707-7_6

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  • DOI: https://doi.org/10.1007/978-3-322-96707-7_6

  • Publisher Name: Vieweg+Teubner Verlag

  • Print ISBN: 978-3-519-03537-4

  • Online ISBN: 978-3-322-96707-7

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