Implementation of picoSpin Benchtop NMR Instruments into Organic Chemistry Teaching Laboratories through Spectral Analysis of Fischer Esterification Products
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Kasey L. Yearty [1] ; Joseph T. Sharp [1] ; Emma K. Meehan [1] ; Doyle R. Wallace [1] ; Douglas M. Jackson [1] ; Richard W. Morrison [1]
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[1] University of Georgia
University of Georgia
Estados Unidos
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- Localización: Journal of chemical education, ISSN 0021-9584, Vol. 94, Nº 7, 2017, págs. 932-935
- Idioma: inglés
- Texto completo no disponible (Saber más ...)
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Resumen
1H NMR analysis is an important analytical technique presented in introductory organic chemistry courses. NMR instrument access is limited for undergraduate organic chemistry students due to the size of the instrument, price of NMR solvents, and the maintenance level required for instrument upkeep. The University of Georgia Chemistry Department recently acquired three picoSpin desktop 1H NMR instruments for the undergraduate organic laboratories. These instruments can sit on a standard lab bench, can analyze samples without NMR solvents, and are easily maintained. In this Fischer esterification experiment, students used unknown starting alcohols to synthesize esters through Fischer esterification. Upon completion of the reaction, students identified the unknown starting alcohol via spectral analyses of the products. Over the course of 4 semesters, 704 out of 940 students (75%) correctly identified the starting alcohol and 71% of students surveyed indicated that 1H NMR spectrum was the most helpful identification tool in their analyses. This experiment established for students the utility of NMR spectral analysis and provided them with the opportunity to employ technology commonly used in academic research facilities.
