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HERO ID
4903563
Reference Type
Journal Article
Title
Synthesis of Bisphenol Z: An Organic Chemistry Experiment
Author(s)
Gregor, RW
Year
2012
Is Peer Reviewed?
Yes
Journal
Journal of Chemical Education
ISSN:
0021-9584
Volume
89
Issue
5
Page Numbers
669-671
DOI
10.1021/ed200293k
Web of Science Id
WOS:000302758000029
Abstract
A student achievable synthesis of bisphenol Z, 4,4'-(cyclohexane-1,1-diyl)diphenol, from the acid-catalyzed reaction of phenol with cyclohexanone is presented. The experiment exemplifies all the usual pedagogy for the standard topic of electrophilic aromatic substitution present in the undergraduate organic chemistry curriculum, while providing the opportunity to create a product that is a member of a family of compounds (including bisphenol A) that is industrially important, but with significant controversy over health and environmental concerns. The synthesis can serve as a springboard for discussion or research on a variety of related topics such as polymer plastic or epoxy resin synthesis, intellectual property and patents, endocrine system disruptors, and environmental toxicology. The experiment has a very low cost of ownership, is reliable at producing yields of 45%, and may be completed in a single laboratory period. In addition, it serves as an example of a reaction that forms an isolable stoichiometric adduct between the product and unreacted reagent (phenol) and is readily differentiated and characterized by melting point, thin-layer chromatography, and H-1 NMR.
Keywords
Second-Year Undergraduate; Laboratory Instruction; Organic Chemistry; Hands-On Learning/Manipulatives; Aromatic Compounds; Electrophilic Substitution; NMR Spectroscopy; Reactions; Synthesis; Thin Layer Chromatography
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