JCE Online Journal of Chemical Education
 | Subscriptions  | Software Orders  | Support  | Contributors  | Advertisers  | 

JCE Print

JCE Digital Library

JCE Software

Only@JCE Online

About JCE


  Home > JCE Print > Journal of Chemical Education > Issues > 2000  > December  >
Research: Science and Education
Carbinolamines and Geminal Diols in Aqueous Environmental Organic Chemistry
Edward T. Urbansky
National Risk Management Research Laboratory, US Envionmental Protection Agency, 26 West Martin Luther King Drive, MS-681, Cincinnati, OH 45268-0001

Cover
December 2000
Vol. 77 No. 12
p. 1644

Abstract
Organic chemistry textbooks generally treat geminal diols as curiosities--exceptions to the stability of the C=O double bond. However, most aldehydes of environmental significance, to wit, trichloroethanal (chloral), methanal (formaldehyde), ethanal (acetaldehyde), and propanal (propionaldehyde), exhibit this behavior. Carbinolamines (hemiaminals) are usually considered to be unstable reaction intermediates of very short lifetime, despite a considerable volume of literature that suggests otherwise. In aqueous solution, carbinolamines can build up to substantial concentrations and play important roles in kinetics of aldehyde reactions, subsequent to formation of aldehydes as ozonation by-products during drinking water disinfection. A few carbinolamines are isolable, although these are not encountered in environmental systems. In general, the minimal conceptual treatment of these chemical species results from the central theme of synthetic utility that quite reasonably dominates organic chemistry courses and textbooks. Nonetheless, a pedagogical consequence is that students may be left with an incorrect perception that these species are unlikely to be encountered in common situations. Accordingly, it is important for teachers and students of environmental chemistry to remember that aqueous chemistry can be quite different from that observed in less polar and sometimes aprotic organic solvents.
More Information
*  Citation
Urbansky, Edward T. J. Chem. Educ. 2000 77 1644.
*  Keywords
Aqueous Solution Chemistry; Environmental Chemistry; Kinetics; Organic Chemistry; Water / Water Chemistry
*  History
Created:
Last Updated:
November 3, 2000
April 15, 2005
  Home > JCE Print > Journal of Chemical Education > Issues > 2000 > December > Page 1644


Subscriptions

JCE HS CLIC

Our Secondary School editors work hard to distill all the JCE materials to produce a fraction of particular interest to high school teachers. We call it CLIC.


Contributions Welcome
JCE welcomes your submission

Advertisers
In recent years we have worked hard to better match our advertisers with our readers. When shopping for chemistry education materials, visit our advertisers' WWW sites first.

Be An Ambassador
Take JCE along on your outreach missions. Copies of the Journal, guest access to JCE Online, our publications catalog, and more are available for your participants.