Measuring Structural and Electronic Effects on Keto-Enol Equilibrium in 1,3-Dicarbonyl Compounds

作者：Smith Kyle T; Young Sherri C; DeBlasio James W; Hamann Christian S^*

来源：Journal of Chemical Education, 2016, 93(4): 790-794.

DOI：10.1021/acs.jchemed.5b00170

• Constitutional Isomers
• Equilibrium
• Hands-On Learning/Manipulatives
• Laboratory Instruction
• NMR Spectroscopy
• Organic Chemistry
• Physical Chemistry
• Problem Solving/Decision Making
• Second-Year Undergraduate
• Upper-Division Undergraduate

Nuclear magnetic resonance (NMR) spectroscopy is an integral part of the undergraduate chemistry curriculum. In addition to structure determination, NMR spectroscopy is used to analyze chemical reactions and equilibria in situ. Determination of the position of equilibria is well-suited to NMR analysis in the undergraduate laboratory as an extension of peak identification and signal integration, and the determination of keto-enol equilibrium remains a popular undergraduate laboratory experiment. Several factors affect the position of keto-enol equilibrium, defined here as K-e/k = [enol]/[keto], including structure (steric bulk, conjugation, electron-withdrawing/donating groups, resonance), temperature, and solvent. A judiciously selected set of compounds that have a common 1,3-dicarbonyl moiety with progressively changing ligands at the 1 and 3 positions is presented. This array allows students to investigate structure-function relationships that affect keto-enol equilibrium in broad selection of compounds for study in both introductory and advanced laboratory approaches. a cumulative fashion and affords instructors a courses using a variety of pedagogic approaches.

• 出版日期2016-4