JCE Online Journal of Chemical EducationDivision of Chemical Education, American Chemical SocietyAmerican Chemical Society
 | Subscriptions  | Software Orders  | Support  | Contributors  | Advertisers  | 

JCE Print

JCE Digital Library

JCE Software

Only@JCE Online

About JCE


 Home > Only@JCE Online > Features > Featured Molecules > 2006 >
Featured Molecules April 2006
""
Microwave-Assisted Heterocyclic Chemistry

The featured molecules for this month come from the Green Chemistry article, "Microwave-Assisted Heterocyclic Chemistry for the Undergraduate Organic Laboratory" by Musiol, Tyman-Szram, and Polanski. The authors give conditions and yields for the solid-phase synthesis of a number of heterocyclic compounds in a microwave oven. Although the jury is still out on the detailed mechanism behind microwave acceleration of reaction rates, there is a great deal of interest in such reactions in the chemical community. Students encountering heterocyclic species for the first time might find it useful to consider the effect of addition of a heteroatom on the electron distribution in the molecule. The Chime plug-in enables the user to construct a qualitative electrostatic potential map, allowing students to visualize this map in three-dimensions. Details of this process are available.

Viewing Requirements

In addition to the static images, two fully manipulable versions (Jmol, MDLChime) of these molecules appear below.

* Download Chime (registration required)

Image of molecule.

Figure 1. benzimidazole

Image of molecule.

Figure 2. succinic anhydride

Image of molecule.

Figure 3. phthalimide

Image of molecule.

Figure 4. piperazine-2,5-dione

Image of molecule.

Figure 5. 2,3-diphenylquinoxaline

Image of molecule.

Figure 6. 5,5-diphenylhydantoin

Image of molecule.

Figure 7. benzoxazinone

Article
*
 Home > Only@JCE Online > Features > Featured Molecules > 2006 > April


JCE Digital Library
JCE DLib