Tuesday, 24 May 2005

This presentation is part of: Organic Posters

Substituent Effects for Two Series of Substituted N-Benzylideneanilines Using NMR Spectroscopy

John Tierney1, Linda M. Mascavage2, and Christopher Dieterick2. (1) Pennsylvania State University, Media, PA, (2) Arcadia University, Glenside, PA

Two series of mono-substituted N-benzylideneanilines, 1 and 2, have been synthesized. The substituents were placed in the C-phenyl ring and the N-phenyl ring at either the 3 or 4 positions. This is a report of preliminary results for substituent effects on 13C chemical shifts in both phenyl rings and at the benzylic carbon in deuterochloroform solution. The effects on the 1H chemical shifts for the methine proton will also be shown.

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