1H NMR analysis of sulfanilamide-based imines synthesized from aromatic aldehydes.
Presenter(s)
Lily Glendenning, Kevin Dang, and Will Gunderson
Abstract
In this project, we focused on the 1H NMR analysis of seven different imines synthesized by combining sulfanilamide, a classic antibacterial agent, with various substituted benzaldehydes. Our 1H NMR analysis provided detailed insights into the precise structures of these compounds, confirming their successful formation and purity beyond what was capable for other characterization methods such as mass spectrometry and IR spectroscopy. Purity analysis and structural verification of these compounds was performed in support of several related projects as part of a CURE-based laboratory experience in CHEM 213.
College
College of Science & Engineering
Department
Chemistry
Campus
Winona
First Advisor/Mentor
Joseph K. West
Start Date
4-24-2025 2:00 PM
End Date
4-24-2025 3:00 PM
Presentation Type
Poster Session
Format of Presentation or Performance
In-Person
Session
2b=2pm-3pm
Poster Number
20
1H NMR analysis of sulfanilamide-based imines synthesized from aromatic aldehydes.
In this project, we focused on the 1H NMR analysis of seven different imines synthesized by combining sulfanilamide, a classic antibacterial agent, with various substituted benzaldehydes. Our 1H NMR analysis provided detailed insights into the precise structures of these compounds, confirming their successful formation and purity beyond what was capable for other characterization methods such as mass spectrometry and IR spectroscopy. Purity analysis and structural verification of these compounds was performed in support of several related projects as part of a CURE-based laboratory experience in CHEM 213.
Comments
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