| Journal Articles: 17 results |
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The Glyoxal Clock Reaction Julie B. Ealy, Alexandra Rodriguez Negron, Jessica Stephens, Rebecca Stauffer, and Stanley D. Furrow The glyoxal clock reaction has been adapted to a general chemistry kinetics lab to determine the order of the reacting species using a Calculator Based Laboratory or LabPro equipment. Ealy, Julie B.; Negron, Alexandra Rodriguez; Stephens, Jessica; Stauffer, Rebecca; Furrow, Stanley D. J. Chem. Educ. 2007, 84, 1965.
Aldehydes / Ketones |
Dyes / Pigments |
Kinetics |
Lewis Acids / Bases |
Mechanisms of Reactions |
Rate Law |
Reactions
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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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Let Us Give Lewis Acid–Base Theory the Priority It Deserves Alan A. Shaffer The Lewis concept is simple yet powerful in its scope, and can be used to help beginning students understand reaction mechanisms more fully. However, traditional approaches to acid-base reactions at the introductory level ignores Lewis acid-base theory completely, focusing instead on proton transfer described by the Br?nsted-Lowry concept. Shaffer, Alan A. J. Chem. Educ. 2006, 83, 1746.
Acids / Bases |
Lewis Acids / Bases |
Lewis Structures |
Mechanisms of Reactions |
Molecular Properties / Structure |
VSEPR Theory |
Covalent Bonding |
Brønsted-Lowry Acids / Bases
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Two "Gas-in-a-Bag" Reactions To Show the Predictive Power of the Relative AcidBase Strength Chart Brett Criswell Describes a demonstration in which two different pairs of solid chemicals mixed in two different Ziploc bags in the presence of a small quantities of water react to produce gases. Students are informed that the reactions are BrnstedLowry acidbase type reactions and must determine which member in each pair will act as the acid and which as the base. Criswell, Brett. J. Chem. Educ. 2006, 83, 1167.
Acids / Bases |
Aqueous Solution Chemistry |
Descriptive Chemistry |
Gases |
Reactions |
Brønsted-Lowry Acids / Bases
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Synthesis and Physical Properties of Liquid Crystals: An Interdisciplinary Experiment Gerald R. Van Hecke, Kerry K. Karukstis, Hanhan Li, Hansford C. Hendargo, Andrew J. Cosand, and Marja M. Fox This experiment features an investigative approach designed for the introductory science or engineering major and integrates concepts in the fields of chemistry, biology, and physics. Derived from faculty research interests, this novel experiment gives students the opportunity to draw conclusions from tests performed to illustrate the connection between molecular structure and macroscopic properties. The chemical synthesis of the compounds studied further enhances the connection between molecular structure and macroscopic physical properties. The results of two separate physical measurements, refractometry and absorption spectroscopy, are combined to calculate a microscopic, but very practical, property of chiral nematic liquidsthe pitch of the helix formed in the liquid crystalline phase. Van Hecke, Gerald R.; Karukstis, Kerry K.; Li, Hanhan; Hendargo, Hansford C.; Cosand, Andrew J.; Fox, Marja M. J. Chem. Educ. 2005, 82, 1349.
Chirality / Optical Activity |
Crystals / Crystallography |
Molecular Properties / Structure |
UV-Vis Spectroscopy |
Acids / Bases |
Esters |
Physical Properties |
Physical Properties
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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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Acids and Bases in Layers: The Stratal Structure of an Ancient Topic Wobbe de Vos and Albert Pilot This article identifies and discusses six successive "layers" that can be recognized in chapters on acids and bases in general chemistry textbooks, each the result of what once was a modernization; the cumulative result of these layers has become problematic, and some learning problems that students have when studying acids and bases become comprehensible when viewed from this perspective. de Vos, Wobbe; Pilot, Albert. J. Chem. Educ. 2001, 78, 494.
Acids / Bases |
Learning Theories |
Lewis Acids / Bases |
Brønsted-Lowry Acids / Bases
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Lewis diagrams (Pavia, Donald L.) Jensen, William P.; Tarr, Donald A. Two reviews for the titled software designed to help students determine Lewis structures of molecules and ions. Jensen, William P.; Tarr, Donald A. J. Chem. Educ. 1988, 65, A271.
Lewis Acids / Bases
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Demonstrations for high school chemistry Castka, Joseph F. A sequence of demonstrations that may serve to initiate and maintain student interest in the development of acid-base theories and bond strength. Castka, Joseph F. J. Chem. Educ. 1975, 52, 394.
Acids / Bases |
Covalent Bonding |
Lewis Acids / Bases |
Brønsted-Lowry Acids / Bases
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Understanding a culprit before eliminating it. An application of Lewis acid-base principles to atmospheric SO2 as a pollutant Brasted, Robert C. The SO2 molecule offers ample opportunities for teaching practical chemistry. [Debut of first run. This feature reappeared in 1986.] Brasted, Robert C. J. Chem. Educ. 1970, 47, 447.
Acids / Bases |
Lewis Acids / Bases |
Atmospheric Chemistry |
Mechanisms of Reactions |
Reactions |
Applications of Chemistry |
Lewis Structures |
Molecular Properties / Structure
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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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Homogeneous catalysis: A reexamination of definitions Leisten, J. A. Considers common questions regarding the action of catalysts by examining various typical examples. Leisten, J. A. J. Chem. Educ. 1964, 41, 23.
Catalysis |
Reactions |
Acids / Bases
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Acids, Bases, and the Chemistry of the Covalent Bond (VanderWerf, Calvin A.) Eblin, Lawrence P.
Eblin, Lawrence P. J. Chem. Educ. 1962, 39, 273.
Acids / Bases |
Covalent Bonding
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Electronegativities in inorganic chemistry. III Sanderson, R. T. The purpose of this paper is to illustrate some of the practical applications of electronegativities and charge distribution. Sanderson, R. T. J. Chem. Educ. 1954, 31, 238.
Atomic Properties / Structure |
Covalent Bonding |
Acids / Bases
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Models illustrating the Lewis theory of acids and bases Herron, Fred Y. The purpose of this article is to describe a method of presenting the Lewis theory of acids and bases by means of cardboard models. Herron, Fred Y. J. Chem. Educ. 1953, 30, 199.
Acids / Bases |
Lewis Acids / Bases |
Molecular Modeling
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