| Journal Articles: 22 results |
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The Discovery-Oriented Approach to Organic Chemistry. 7. Rearrangement of trans-Stilbene Oxide with Bismuth Trifluoromethanesulfonate and Other Metal Triflates James E. Christensen, Matthew G. Huddle, Jamie L. Rogers, Herbie Yung, and Ram S. Mohan
Presents a microscale, green organic chemistry laboratory experiment that illustrates the utility of metal triflates, especially bismuth triflate, as a Lewis acid catalyst. Bismuth compounds are especially attractive for use as catalysts in organic synthesis because of their low toxicity, low cost, and ease of handling.
Christensen, James E.; Huddle, Matthew G.; Rogers, Jamie L.; Yung, Herbie; Mohan, Ram S. J. Chem. Educ. 2008, 85, 1274.
Catalysis |
Epoxides |
Green Chemistry |
Lewis Acids / Bases |
Mechanisms of Reactions |
Microscale Lab |
NMR Spectroscopy
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Concerning Lewis Acid–Base Theory for Proton Transfer Lawrence J. Sacks
Counterpoint commentary in response to a suggestion that the Lewis acidbase approach be applied to reactions such as ammoniawater and HClwater.
Sacks, Lawrence J. J. Chem. Educ. 2007, 84, 1415.
Acids / Bases |
Lewis Acids / Bases |
Theoretical Chemistry |
Brønsted-Lowry Acids / Bases
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J. Chem Ed. 2007, 84, 1056–1061
The article Getting the Weights of Lewis Structures out of Hckel Theory: HckelLewis Configuration Interaction (HL-CI) has an incorrectly printed table on p. 1059.
J. Chem. Educ. 2007, 84, 1277.
Lewis Acids / Bases
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Synthesis of Methyl Diantilis, a Commercially Important Fragrance William H. Miles and Katelyn B. Connell
Describes the synthesis of a family of fragrances, including the commercially important Methyl Diantilis, and provides an excellent introduction to intellectual property laws.
Miles, William H.; Connell, Katelyn B. J. Chem. Educ. 2006, 83, 285.
Alcohols |
Food Science |
Catalysis |
Ethers |
Industrial Chemistry |
IR Spectroscopy |
Lewis Acids / Bases |
NMR Spectroscopy |
Oxidation / Reduction |
Synthesis
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Reaction to "Chemistry Is Not a Laboratory Science" Lawrence J. Sacks
Stephen Hawkes has stirred us to reconsider whether, in fact, chemistry is a laboratory science by positing that lab work does not enhance students understanding of chemistrys centrality, but makes chemistry an irrelevance. This sweeping generalization of what some (maybe even most) labs do is further confounded by a fallacious premise; hence, the major thrust of the proposition likely will beand well should beviewed with utmost skepticism.
Sacks, Lawrence J. J. Chem. Educ. 2005, 82, 997.
Laboratory Computing / Interfacing |
Learning Theories |
Lewis Acids / Bases |
Nonmajor Courses |
Theoretical Chemistry |
Student-Centered Learning
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Reaction to "Chemistry Is Not a Laboratory Science" Lawrence J. Sacks
In response to Stephen Hawkes Commentary, I think the crucial point is whether the students learn to appreciate the intellectual beauty of science and understand the relatively small number of simple yet profound scientific principles which govern so much of our everyday experiences. Many non-science majors are obviously disinterested in the laboratory work in introductory courses.
Sacks, Lawrence J. J. Chem. Educ. 2005, 82, 997.
Laboratory Computing / Interfacing |
Student-Centered Learning |
Learning Theories |
Lewis Acids / Bases |
Nonmajor Courses |
Theoretical Chemistry
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Lewis Acid–Base, Molecular Modeling, and Isotopic Labeling in a Sophomore Inorganic Chemistry Laboratory Chip Nataro, Michelle A. Ferguson, Katherine M. Bocage, Brian J. Hess, Vincent J. Ross, and Daniel T. Swarr
Computational methods can be introduced to simulate IR spectra and to view the HOMO of the Lewis base and the LUMO of the Lewis acid. In addition to the computational exercise, NaBD4 can be used in the synthesis of the adduct in place of NaBH4. This allows the students to observe the effect of isotopic labeling on IR spectra.
Nataro, Chip; Ferguson, Michelle A.; Bocage, Katherine M.; Hess, Brian J.; Ross, Vincent J.; Swarr, Daniel T. J. Chem. Educ. 2004, 81, 722.
Lewis Acids / Bases |
Molecular Modeling |
Isotopes |
IR Spectroscopy |
Laboratory Computing / Interfacing
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Acid–Base Titrations in Nonaqueous Solvents and Solvent Mixtures Lajos Barcza and Ágnes Buvári-Barcza
Discussion of acid-base theory, the role of hydrogen bonding in acid-base reactions, and promoting, leveling, and differentiating effects.
Barcza, Lajos; Buvári-Barcza, Ágnes. J. Chem. Educ. 2003, 80, 822.
Acids / Bases |
Equilibrium |
Solutions / Solvents |
Titration / Volumetric Analysis |
Enrichment / Review Materials |
Hydrogen Bonding |
Lewis Acids / Bases |
Brønsted-Lowry Acids / Bases
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Organic Chemistry (by Maitland Jones, Jr. ) Michael S. Holden
The general framework that Jones uses is that of Lewis acids reacting with Lewis bases, with an emphasis on the interaction of filled and empty orbitals. Again and again, as you work your way through the text, there are examples of reactions being explained by the overlap of orbitals.
Holden, Michael S. J. Chem. Educ. 1998, 75, 291.
Lewis Acids / Bases
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The Synthesis, Characterization, and Lewis Acidity of SnI2 and SnI4 Richard W. Schaeffer, Benny Chan, Michael Molinaro, Susan Morissey, Claude H. Yoder, Carolyn S. Yoder, and Stephanie Shenk
In this project the student has the opportunity to learn about: a) the direct synthesis of compounds from the elements, b) stoichiometry and limiting reagent, c) isolation by recrystallization, d) use of inert atmosphere, e) identification by melting point, gravimetric analysis, powder x-ray diffraction, and NMR spectroscopy, and f) at least one method for determination of relative Lewis acidity.
Schaeffer, Richard W. ; Chan, Benny ; Molinaro, Michael; Morissey, Susan ; Yoder, Claude H.; Yoder, Carolyn S.; Shenk, Stephanie. J. Chem. Educ. 1997, 74, 575.
Acids / Bases |
Synthesis |
Stoichiometry |
Lewis Acids / Bases |
NMR Spectroscopy
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Optical Basicity: A Practical Acid-Base Theory for Oxides and Oxyanions J. A. Duffy
The optical basicity concept relies on the Lewis approach to acids and bases and was developed for dealing with chemical problems in non-aqueous, non-protonic media such as silicates, phosphates and borates which are important in glass making and (as slags) for refining steel.
Duffy, J. A. J. Chem. Educ. 1996, 73, 1138.
Acids / Bases |
Lewis Acids / Bases
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Hard and Soft Acid-Base Behavior in Aqueous Solution: Steric Effects Make Some Metal Ions Hard: A Quantitative Scale of Hardness-Softness for Acids and Bases Robert D. Hancock and Arthur E. Martell
The idea of hard and Soft Acids and Bases (HSAB), developed by R. G. Pearson some 30 years ago, has been used as a unifying principle in several texts. In this article, the behaviour of HSAB in aqueous solution is addressed. A quantitative scale of hardness-softness for acids and bases is presented also.
Robert D. Hancock and Arthur E. Martell. J. Chem. Educ. 1996, 73, 654.
Quantitative Analysis |
Lewis Acids / Bases |
Solutions / Solvents |
Metals |
Coordination Compounds
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Epoxidation of Alpha-Methylstyrene and its Lewis Acid Rearrangement to 2-Phenylpropanal David L. Garin, Melissa Gamber, and Bradley J. Rowe
This undergraduate organic lab experiment includes procedures for the peracid epoxidation of an olefin and the Lewis acid rearrangement of an epoxide to a carbonyl compound.
Garin, David L.; Gamber, Melissa; Rowe, Bradley J. J. Chem. Educ. 1996, 73, 555.
Lewis Acids / Bases |
Spectroscopy |
NMR Spectroscopy |
UV-Vis Spectroscopy |
Gas Chromatography |
IR Spectroscopy |
Aldehydes / Ketones
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Beta-keto esters from tin(II) chloride catalyzed reactions of aldehydes with ethyl diazoacetate: An undergraduate laboratory experiment drawn from the current literature Brockwell, Joyce C.; Holmquist, Christopher R.
This is an experimental procedure for producing longer-chain keto esters from unconjugated aldehydes on reaction with ethyl diazoacetate catalyzed by Lewis acids for use in an undergraduate laboratory.
Brockwell, Joyce C.; Holmquist, Christopher R. J. Chem. Educ. 1992, 69, 68.
Catalysis |
Synthesis |
Lewis Acids / Bases |
Aldehydes / Ketones |
Esters
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Zinc enzymes Bertini, I.; Luchinat, C.; Monnanni, R.
The role played by catalytic and noncatalytic zinc in biochemical systems. From the "State of the Art Symposium: Bioinorganic Chemistry", held at the ACS meeting, Miami, 1985.
Bertini, I.; Luchinat, C.; Monnanni, R. J. Chem. Educ. 1985, 62, 924.
Enzymes |
Bioinorganic Chemistry |
Lewis Acids / Bases |
Proteins / Peptides
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Metal complexes as color indicators for solvent parameters Soukup, Rudolf W.; Schmid, Roland
Review of the use of metal ions as color indicators for both the sigma-donor and sigma-acceptor abilities of solvents; briefly describes several experiments involving such metal complexes.
Soukup, Rudolf W.; Schmid, Roland J. Chem. Educ. 1985, 62, 459.
Metals |
Coordination Compounds |
Lewis Acids / Bases
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Lewis acid-base equilibria. An undergraduate laboratory experiment Brice, L. K.
Describes an experiment involving the spectrophotometric determination of formation constants of Lewis adducts formed between metal halides and organic bases in diethyl ether as a solvent.
Brice, L. K. J. Chem. Educ. 1973, 50, 430.
Acids / Bases |
Lewis Acids / Bases |
Equilibrium |
Quantitative Analysis
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Hard and soft acids and bases, HSAB, part II: Underlying theories Pearson, Ralph G.
Explores possible explanations for and presents applications of the principles of hard and soft acids and bases.
Pearson, Ralph G. J. Chem. Educ. 1968, 45, 643.
Acids / Bases |
Lewis Acids / Bases |
Aqueous Solution Chemistry |
Solutions / Solvents |
Ionic Bonding |
Covalent Bonding
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Hard and soft acids and bases, HSAB, part 1: Fundamental principles Pearson, Ralph G.
Using the principles of hard and soft acids and bases to estimate the strength and softness of an acid or base.
Pearson, Ralph G. J. Chem. Educ. 1968, 45, 581.
Acids / Bases |
Lewis Acids / Bases |
Coordination Compounds
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Lewis acid-base titration in fused salts Schlegel, James M.
Dichromate ion, a Lewis acid, is titrated with carbonate ion, a Lewis base, in a fused KNO3-NaNO3 solvent.
Schlegel, James M. J. Chem. Educ. 1966, 43, 362.
Lewis Acids / Bases |
Acids / Bases |
Titration / Volumetric Analysis |
Quantitative Analysis
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Letter to the editor Onwood, D. P.
Discusses variations in the usage of the terms "acid" and "base," including Lowry-Bronsted and Lewis systems.
Onwood, D. P. J. Chem. Educ. 1966, 43, 335.
Acids / Bases |
Lewis Acids / Bases |
Nomenclature / Units / Symbols
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Acidity measurements with indicators in glacial acetic acid Kolling, Orland W.
In the measurement of acidity in glacial acetic acid solutions of acids as strong as perchloric, the color change of a basic indicator may be used.
Kolling, Orland W. J. Chem. Educ. 1958, 35, 452.
Acids / Bases |
Aqueous Solution Chemistry |
Lewis Acids / Bases
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