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

Comments

No poster file.

Share

COinS
 
Apr 24th, 2:00 PM Apr 24th, 3:00 PM

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.