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A Mixed Aldol Condensation-Michael Addition Experiment
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Abstract
This article describes the anlysis of the recrystallized products of a mixed aldol condensation between symmetrical ketones and aromatic aldehydes.
Keywords (Audience):
Second-Year UndergraduateKeywords (Domain):
Organic ChemistryKeywords (Pedagogy):
Hands-On Learning / ManipulativesKeywords (Subject):
Aldehydes / KetonesCiting Articles
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This article has been cited by 3 ACS Journal articles (3 most recent appear below).
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Thomas P. Clausen , Thomas K. Green and Benjamin SteinerJournal of Chemical Education2008 85 (5), 692In teaching organic chemistry laboratory at this university, we eliminated the use of "canned" experiments from textbooks. Instead, we present students with literature studies that form the basis of developing new unpublished experiments to answer ...
A Nitration Reaction Puzzle for the Organic Chemistry Laboratory
Milton J. Wieder and Russell BarrowsJournal of Chemical Education2008 85 (4), 549A Nitration Reaction Puzzle for the Organic Chemistry Laboratory
Milton J. Wieder and Russell BarrowsJournal of Chemical Education2008 85 (4), 549Treatment of phenylacetic acid with 90% HNO3 yields a product, I, whose observed melting point is 175–179 °C and whose equivalent weight is approximately 226 grams. Treatment of phenylacetic acid with 70% HNO3 yields a product, II, whose observed melting ...
A Solvent-Free Claisen Condensation Reaction for the Organic Laboratory
John J. Esteb and Matthew B. StocktonJournal of Chemical Education2003 80 (12), 1446A Solvent-Free Claisen Condensation Reaction for the Organic Laboratory
John J. Esteb and Matthew B. StocktonJournal of Chemical Education2003 80 (12), 1446An experiment involving the Claisen condensation reaction for a first-year organic chemistry laboratory is presented. Claisen condensations are routinely covered in organic textbooks but owing to the long reaction times required to reach equilibrium in ...
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History
- Received: August 03, 2009
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