Contact Information

Author
  • Thottumkara K. Vinod
  • Professor
  • Chemistry
  • Western Illinois Univ.
  • Macomb, IL 61455
Email
Phone
(309) 298 - 1379
Website

Oxidation of Aromatic Aldehydes using Oxone

Author Contact: mftkv@wiu.edu

Summary

One of the main advantages of doing green chemistry is that it can often be done on the bench top without the need of a fume-hood. In this experiment water and ethanol are the only solvents used for both the reaction and purification steps and oxone is a safe oxidant whose only by-product is potassium sulfate.

The oxidation of aromatic aldehydes using oxone allows instructors to discuss green chemistry, oxidation reactions and recrystallizations. Other topics include the use of melting points and NMR for characterization.

Included are supplemental materials which provide instructor notes, student lab procedure, a list of necessary materials, spectroscopic data and the proposed reaction mechanism.

Summary prepared September 2008 by Douglas M. Young at the University of Oregon.

Source

Gandhari, R.; Maddukuri, P. P.; Vinod, T. K. J. Chem. Educ., Print 2007, 84, pp 852-854.

J. Chem. Educ. (Abstract only)

Category Descriptors

Chemistry Concepts
  • Aldehydes/Ketones
  • Aqueous Solution Chemistry
  • Carbonyl Chemistry
  • Oxidation/Reduction Chemistry
Laboratory Techniques
  • Melting Points and Melting Ranges
  • NMR Spectroscopy
  • Recrystallization
  • Vacuum Filtration
Green Chemistry Principles
  • Design Less Hazardous Chemical Syntheses
  • Prevent Waste
  • Use Safer Solvents/Reaction Conditions
Chemistry Subdiscipline
  • Organic Chemistry
Target Audience
  • Colleges/Universities
Source
  • Journal Articles