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Journal Articles: 32 results
A Simple Laboratory Experiment To Determine the Kinetics of Mutarotation of D-Glucose Using a Blood Glucose Meter  Carlos E. Perles and Pedro L. O. Volpe
A simple commercial blood glucose meter is used to follow the kinetics of mutarotation of D-glucose in aqueous solution. The results may be compared with those obtained using an automatic polarimeter.
Perles, Carlos E.; Volpe, Pedro L. O. J. Chem. Educ. 2008, 85, 686.
Aqueous Solution Chemistry |
Bioanalytical Chemistry |
Carbohydrates |
Chirality / Optical Activity |
Enzymes |
Kinetics |
Solutions / Solvents |
Stereochemistry
A Simple Method for Drawing Chiral Mononuclear Octahedral Metal Complexes  Aminou Mohamadou and Arnaud Haudrechy
This article presents a simple and progressive method to draw all of the octahedral complexes of coordination units with at least two different monodentate ligands and show their chiral properties.
Mohamadou, Aminou; Haudrechy, Arnaud. J. Chem. Educ. 2008, 85, 436.
Asymmetric Synthesis |
Chirality / Optical Activity |
Coordination Compounds |
Diastereomers |
Enantiomers |
Molecular Properties / Structure |
Stereochemistry |
Transition Elements
Can a Non-Chiral Object Be Made of Two Identical Chiral Moieties?  Jean François LeMaréchal
Uses the cut of an apple to show that the association of identical chiral moieties can form a non-chiral object.
LeMaréchal, Jean François. J. Chem. Educ. 2008, 85, 433.
Chirality / Optical Activity |
Coordination Compounds |
Enantiomers |
Group Theory / Symmetry |
Stereochemistry |
Transition Elements
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 liquids┬Łthe 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
"Dishing Out" Stereochemical Principles  Harold Hart
Demonstrating the concepts of chiral centers and enantiomers using plastic dishes.
Hart, Harold. J. Chem. Educ. 2001, 78, 1632.
Chirality / Optical Activity |
Molecular Modeling |
Stereochemistry |
Molecular Properties / Structure |
Enantiomers
Demonstrating Chirality: Using a Mirror with Physical Models to Show Non-superimposability of Chiral Molecules with Their Mirror Images  Michael J. Collins
Using a mirror with physical models to show non-superimposability of chiral molecules with their mirror images.
Collins, Michael J. J. Chem. Educ. 2001, 78, 1484.
Chirality / Optical Activity |
Enantiomers |
Molecular Modeling |
Molecular Properties / Structure
Introducing Stereochemistry to Non-science Majors  Hannia Luján-Upton
Two exercises to introduce concepts associated with stereochemistry such as "sameness", superimposability, chirality, enantiomers, optical activity, polarimetry, and racemic mixtures; one compares chirality in hands with the achiral nature of two textbooks, the other involves a murder mystery.
Luján-Upton, Hannia. J. Chem. Educ. 2001, 78, 475.
Chirality / Optical Activity |
Stereochemistry |
Nonmajor Courses |
Molecular Properties / Structure
Put the Body to Them!  Perkins, Robert R.
Examples of chemistry demonstrations involving student participation, including quantized states and systems, boiling point trends, intermolecular vs. intramolecular changes, polar/nonpolar molecules, enantiomers and diastereomers, and chromatography.
Perkins, Robert R. J. Chem. Educ. 1995, 72, 151.
Chromatography |
Physical Properties |
Phases / Phase Transitions / Diagrams |
Molecular Properties / Structure |
Chirality / Optical Activity |
Quantum Chemistry |
Diastereomers |
Enantiomers
Transformation of chemistry experiments into real world contexts   Bayer, Richard; Hudson, Bud; Schneider, Jane
Some background on the importance of using lasers to teach concepts in general chemistry and examples of demonstrations under development.
Bayer, Richard; Hudson, Bud; Schneider, Jane J. Chem. Educ. 1993, 70, 323.
Lasers |
Chirality / Optical Activity |
Covalent Bonding
Representing isomeric structures: Five applications.  Thall, Edwin.
Five applications of a new method that the author calls Representing Isomeric Structures, in which arrows are used to point to unique sites on the carbon skeleton to represent functional groups.
Thall, Edwin. J. Chem. Educ. 1992, 69, 447.
Stereochemistry |
Molecular Properties / Structure |
Chirality / Optical Activity |
Enantiomers
Polarized light and rates of chemical reactions  Weir, John J.
This experiment provides the opportunity to introduce the principles of reaction kinetics, polarized light, and the chemistry of optically active compounds; the rate of the acid-catalyzed hydrolysis of sucrose to glucose and fructose is determined.
Weir, John J. J. Chem. Educ. 1989, 66, 1035.
Rate Law |
Kinetics |
Chirality / Optical Activity |
Carboxylic Acids
A demonstration of the optical activity of a pair of enantiomers  Knauer, Bruce
Uses the enantiomers (S)-(+)-carvone and (R)-(-)-carvone and a polarizing sheet to illustrate optical activity.
Knauer, Bruce J. Chem. Educ. 1989, 66, 1033.
Chirality / Optical Activity |
Enantiomers
Change in optical rotation with wavelength  Koubek, Edward; Quinn, H.
Illustrates the effect of an optically active material (Karo corn syrup) on plane-polarized light.
Koubek, Edward; Quinn, H. J. Chem. Educ. 1989, 66, 853.
Photochemistry |
Chirality / Optical Activity
Lecture demonstrations for organic/ biochemistry allied health courses  Deavor, James P.
Simple demonstrations on enantiomeric pairs and protein structure.
Deavor, James P. J. Chem. Educ. 1988, 65, 622.
Enantiomers |
Chirality / Optical Activity |
Proteins / Peptides |
Nonmajor Courses |
Amino Acids
Some ideas from the past  Kolb, Doris, editor
Demonstrations from past issues of the Journal, including the common ion effect, the silver tree, crystal formation from supersaturated solutions, making iron passive with nitric acid, optical activity, carbon dioxide in human breath, and amphoteric hydroxides.
Kolb, Doris, editor J. Chem. Educ. 1987, 64, 805.
Aqueous Solution Chemistry |
Chirality / Optical Activity |
Acids / Bases
Synthesis and evaluation of the sex pheromone of the bagworm moth  Schwarz, Meyer; Klun, J. A.
Several possible student-oriented experiments at different educational levels can look into the interesting chemistry involved in a naturally occurring optically active pheromone.
Schwarz, Meyer; Klun, J. A. J. Chem. Educ. 1986, 63, 1014.
Undergraduate Research |
Natural Products |
Synthesis |
Qualitative Analysis |
Chirality / Optical Activity
A simple polarimeter and experiments utilizing an overhead projector  Dorn, H. C.; Bell, H.; Birkett, T.
Design and application of an overhead polarimeter that relies on small amounts of chiral solution and provides a "dual beam" light source for direct comparison of plane-polarized light emerging from chiral and achiral media.
Dorn, H. C.; Bell, H.; Birkett, T. J. Chem. Educ. 1984, 61, 1106.
Laboratory Equipment / Apparatus |
Chirality / Optical Activity |
Stereochemistry |
Molecular Properties / Structure
R/S: Apple stereochemistry program  Barone, Rene; Meyer, Roger; Arbelot, Michel
51. Bits and pieces, 20. Computer program for helping students to learn R/S conventions.
Barone, Rene; Meyer, Roger; Arbelot, Michel J. Chem. Educ. 1984, 61, 524.
Stereochemistry |
Molecular Properties / Structure |
Chirality / Optical Activity |
Enantiomers |
Enrichment / Review Materials
Absolute configuration in a Fischer projection: a simple approach  Bhushan, Ravi; Bhattacharjee, G.
First year undergraduates find it hard to assign absolute configuration to a chiral center when the lowest priority group is either to the left or right of the horizontal line.
Bhushan, Ravi; Bhattacharjee, G. J. Chem. Educ. 1983, 60, 191.
Chirality / Optical Activity |
Molecular Properties / Structure |
Molecular Modeling
Optical Activity  Mickey, Charles D.
Historical background of stereoisomerism, the properties of light, the principles of a polarimeter, and optically active compounds.
Mickey, Charles D. J. Chem. Educ. 1980, 57, 442.
Stereochemistry |
Chirality / Optical Activity |
Molecular Properties / Structure |
Enantiomers
Rotation of plane-polarized light: A simple model  Hill, Roger R.; Whatley, Barrie G.
A simple model that explains why enantiomers of a chiral compound rotate light in different directions.
Hill, Roger R.; Whatley, Barrie G. J. Chem. Educ. 1980, 57, 306.
Photochemistry |
Molecular Modeling |
Chirality / Optical Activity |
Stereochemistry |
Enantiomers |
Molecular Properties / Structure
Chirality, diastereoisomerism, and the Narwhal  Stirling, C. J.
There are many simple examples of enantiomeric objects, both natural and man-made and their static interrelationship is directly and tellingly examined with the aid of a mirror.
Stirling, C. J. J. Chem. Educ. 1978, 55, 32.
Enantiomers |
Chirality / Optical Activity
Synthesis and properties of an optically active complex: A polarimeter experiment for general chemistry  Hunt, Harold R., Jr.
Synthesizing and determining the optical rotation of d-Co(phen)3(ClO4)3.2H2O.
Hunt, Harold R., Jr. J. Chem. Educ. 1977, 54, 710.
Chirality / Optical Activity |
Molecular Properties / Structure |
Stereochemistry |
Synthesis |
Coordination Compounds
Rediscovery in a course for nonscientists. Use of molecular models to solve classical structural problems  Wood, Gordon W.
Describes exercises using simple ball and stick models that students with no chemistry background can solve in the context of the original discovery.
Wood, Gordon W. J. Chem. Educ. 1975, 52, 177.
Molecular Modeling |
Molecular Properties / Structure |
Chirality / Optical Activity |
Enantiomers |
Nonmajor Courses
A simple demonstration of enantiomerism  Richards, K. E.
Design for a wooden box containing a mirror that uses a molecular model to demonstrate enantiomerism.
Richards, K. E. J. Chem. Educ. 1973, 50, 632.
Molecular Properties / Structure |
Molecular Modeling |
Stereochemistry |
Enantiomers |
Chirality / Optical Activity
An overhead projection demonstration of optical activity  Hill, John W.
An overhead projection demonstration of optical activity the makes use of two polarizing lenses and an optically active compound.
Hill, John W. J. Chem. Educ. 1973, 50, 574.
Chirality / Optical Activity |
Molecular Properties / Structure |
Stereochemistry |
Carbohydrates
Construction and uses of an inexpensive polarimeter  Vennos, Mary S.
Presents a design of an inexpensive polarimeter and its use to determine the specific rotation of sucrose and the concentration of an unknown sucrose solution.
Vennos, Mary S. J. Chem. Educ. 1969, 46, 459.
Laboratory Equipment / Apparatus |
Photochemistry |
Chirality / Optical Activity |
Enantiomers |
Instrumental Methods |
Noncovalent Interactions
A TV lecture demonstration of optical activity  Henderson, Giles L.
This demonstration relies on a television camera and polarimeter optics.
Henderson, Giles L. J. Chem. Educ. 1967, 44, 765.
Chirality / Optical Activity
Optical rotation  Evans, J. O. M.; Tietze, H. R.
The angle of rotation of sucrose can be easily determined using this simple demonstration.
Evans, J. O. M.; Tietze, H. R. J. Chem. Educ. 1964, 41, A973.
Molecular Properties / Structure |
Chirality / Optical Activity |
Enantiomers
Systematic names for the tartaric acids  Baxter, J. N.
Examines the use of the small capital letters D and L in naming tartaric acids.
Baxter, J. N. J. Chem. Educ. 1964, 41, 619.
Nomenclature / Units / Symbols |
Acids / Bases |
Carbohydrates |
Chirality / Optical Activity |
Enantiomers
A mailing-tube polarimeter  Shaw, William H. R.
This simple but effective polarimeter is constructed from a cardboard tube and a small square of polarizing film.
Shaw, William H. R. J. Chem. Educ. 1955, 32, 10.
Chirality / Optical Activity |
Molecular Properties / Structure
Miscellaneous experiments  Damerel, Charlotte I.
Offers three demonstrations, the first involving molecular models illustrating the generation of optical isomers in a laboratory synthesis; the second demonstrating that liquid sodium chloride conducts and electric current; and the third examining the flow of electric current in an electrochemical galvanic cell.
Damerel, Charlotte I. J. Chem. Educ. 1952, 29, 296.
Molecular Modeling |
Molecular Properties / Structure |
Chirality / Optical Activity |
Enantiomers |
Conductivity |
Electrochemistry |
Electrolytic / Galvanic Cells / Potentials