| Journal Articles: 26 results |
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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
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Synthesis of Anomeric Methyl Fructofuranosides and Their Separation on an Ion-exchange Resin Erkki Nurminen, Päivi Poijärvi, Katja Koskua, and Jari Hovinen
Treatment of d-fructose with methanol in the presence of acid as a catalyst gives a mixture of methyl--d-fructopyranoside, methyl-a-D-fructofuranoside, and methyl--d- fructofuranoside, which are separated on an ion exchange column and characterized polarimetrically.
Nurminen, Erkki; Poijärvi, Päivi; Koskua, Katja; Hovinen, Jari. J. Chem. Educ. 2007, 84, 1480.
Carbocations |
Chirality / Optical Activity |
Chromatography |
Ion Exchange |
NMR Spectroscopy |
Synthesis |
Thin Layer Chromatography |
Carbohydrates
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CARBOHYDECK: A Card Game To Teach the Stereochemistry of Carbohydrates Manuel João Costa
This paper describes CARBOHYDECK, a card game that may replace or complement lectures identifying and differentiating monosaccharide isomers.
Costa, Manuel João. J. Chem. Educ. 2007, 84, 977.
Aldehydes / Ketones |
Carbohydrates |
Molecular Properties / Structure |
Stereochemistry |
Enrichment / Review Materials |
Student-Centered Learning
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Essentials of Carbohydrate Chemistry and Biochemistry, 2nd Edition (Thisbe K. Lindhorst) David J. A. Schedler
This book is aptly named: it is a well organized, well written presentation of the essentials of carbohydrate chemistry and their relationship to biochemistry.
Schedler, David J. A. J. Chem. Educ. 2004, 81, 808.
Carbohydrates
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Use of Optical Rotation and NMR Signal Counting To Identify Common Aldoses John Almy
An inexpensive, small scale experiment for second semester organic students describes the unambiguous identification of a common aldose "unknown" from five possible candidates: glucose, mannose, galactose, arabinose, or xylose
Almy, John. J. Chem. Educ. 2004, 81, 708.
NMR Spectroscopy |
Carbohydrates |
Microscale Lab |
Molecular Properties / Structure |
Stereochemistry
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Preparation of a D-Glucose-Derived Alkene. An E2 Reaction for the Undergraduate Organic Chemistry Laboratory Peter Norris and Andrew Fluxe
Synthesis of four carbohydrate derivatives that highlight techniques such as inert atmosphere work, rotary evaporators, and flash column chromatography.
Norris, Peter; Fluxe, Andrew. J. Chem. Educ. 2001, 78, 1676.
Carbohydrates |
NMR Spectroscopy |
Synthesis |
Alkenes |
Elimination Reactions |
Chromatography
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Surfactant-Induced Osazone Formation at Room Temperature K. Nagajyothi, P. S. Raghavan, and R. Gopalan
Using surfactants for speedy and easy identification of reducing sugars without heating.
Nagajyothi, K.; Raghavan, P. S.; Gopalan, R. J. Chem. Educ. 2001, 78, 728.
Catalysis |
Micelles |
Surface Science |
Carbohydrates |
Qualitative Analysis
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A Very Simple Method Way to Convert Haworth Representation to Zigzag Representation Janine Cossy and Véronique Bellosta
A very simple method to convert Haworth representation of hexoses and pentoses to zigzag representation is proposed
Cossy, Janine; Bellosta, Véronique. J. Chem. Educ. 1998, 75, 1307.
Carbohydrates |
Nomenclature / Units / Symbols |
Stereochemistry |
Molecular Properties / Structure
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Protecting Groups in Carbohydrate Chemistry Sigthór Pétursson
The most important protecting groups in carbohydrate chemistry are reviewed. The paper is aimed at those beginning to specialize in synthetic carbohydrate chemistry and at teachers with other specialties who wish to go beyond the content of general organic chemistry textbooks.
Petursson, Sigthor. J. Chem. Educ. 1997, 74, 1297.
Carbohydrates |
Molecular Properties / Structure |
Synthesis
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Carbohydrate Dehydration Demonstrations David A. Dolson, Rubin Battino, Trevor M. Letcher, K. H. Pegel, and N. Revaprasadu
Study of the dehydration of a carbohydrate by sulfuric acid and variables that influence the reaction (including type of sugar, sugar granule size, and amount of water added to sugar).
Dolson, David A.; Battino, Rubin; Letcher, Trevor M.; Pegel, K. H.; Revprasadu, N. J. Chem. Educ. 1995, 72, 927.
Carbohydrates |
Reactions
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Inclass interactive worksheets for organic chemistry Ostercamp, Daryl L.
The author has designed two in-class worksheets for use near the end of a two semester organic chemistry course, one dealing with mono- and disaccharides and the second dealing with alpha-amino acids and dipeptides.
Ostercamp, Daryl L. J. Chem. Educ. 1992, 69, 318.
Carbohydrates |
Amino Acids |
Proteins / Peptides
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NMR and the structure of D-glucose Gurst, Jerome E.
A discussion of typical organic chemistry textbook treatment of NMR evidence of glucose structure.
Gurst, Jerome E. J. Chem. Educ. 1991, 68, 1003.
Carbohydrates |
NMR Spectroscopy
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Binary representation in carbohydrate nomenclature McGinn, Clifford J.; Wheatley, William B.
A binary notation is used to indicate the structure of carbohydrates.
McGinn, Clifford J.; Wheatley, William B. J. Chem. Educ. 1990, 67, 747.
Carbohydrates |
Nomenclature / Units / Symbols |
Stereochemistry
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A mnemonic scheme for interconverting Fischer projections of open-chain monosaccharides and Haworth projections of corresponding alpha- and beta-anomeric forms Mitschele, Jonathan
Rules that make it easy for students to recognize alpha- and beta-anomers and the D and L forms of monosaccharides in their Hawthorn projections.
Mitschele, Jonathan J. Chem. Educ. 1990, 67, 553.
Carbohydrates |
Molecular Properties / Structure |
Stereochemistry
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Biochemistry laboratory for the freshman chemistry curriculum Falk, Peter M.
Intended to introduce students to two important biochemical principles: the study of biomolecules and metabolism.
Falk, Peter M. J. Chem. Educ. 1989, 66, 944.
Metabolism |
Carbohydrates |
Lipids |
Proteins / Peptides |
Plant Chemistry
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Carbohydrate stereochemistry Shallenberger, Robert S.; Wienen, Wanda J.
A progress in the development of general stereochemical principles has been significantly influenced by studies that led to determination of the crystalline and solution structures of sugars, the subject of carbohydrate chemistry is developed here in historical fashion.
Shallenberger, Robert S.; Wienen, Wanda J. J. Chem. Educ. 1989, 66, 67.
Carbohydrates |
Stereochemistry
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A laboratory exercise in the determination of carbohydrate structures White, Bernard J.; Robyt, John F.
A laboratory exercise in the determination of carbohydrate structures that introduces students to important aspects of science, such as designing experiments, making observations, and testing hypotheses.
White, Bernard J.; Robyt, John F. J. Chem. Educ. 1988, 65, 164.
Carbohydrates
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Simple rule for the conversion of Fischer monosaccharide projection formulas into Haworth representations Argiles, J. M.
Many students struggle with memorizing Haworth structures, the authors provide some insight on this topic to help students.
Argiles, J. M. J. Chem. Educ. 1986, 63, 927.
Molecular Properties / Structure |
Enantiomers |
Chirality / Optical Activity |
Carbohydrates |
Molecular Modeling
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The chemical composition of the cell Holum, John R.
A broad outline of the chemical substances that occur in most cells.
Holum, John R. J. Chem. Educ. 1984, 61, 877.
Biological Cells |
Lipids |
Carbohydrates |
Proteins / Peptides
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Maple syrup production as a laboratory exercise Burt, Norman E.
A primer to maple syrup production, a source for a variety of laboratory exercises.
Burt, Norman E. J. Chem. Educ. 1973, 50, 623.
Applications of Chemistry |
Consumer Chemistry |
Carbohydrates
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Questions [and] Answers Campbell, J. A.
Five questions requiring an application of chemical principles and their solutions.
Campbell, J. A. J. Chem. Educ. 1973, 50, 128.
Enrichment / Review Materials |
Proteins / Peptides |
pH |
Carbohydrates |
Molecular Properties / Structure
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Polyethylene and pipecleaner models of biological polymers Pollard, Harvey Bruce
An accurate method for modeling polysaccharides, nucleic acids, and proteins involves the use of pipecleaners, polyethylene tubing, and proteins.
Pollard, Harvey Bruce J. Chem. Educ. 1966, 43, 327.
Proteins / Peptides |
Molecular Modeling |
Molecular Properties / Structure |
Carbohydrates
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Evidence for the configuration on carbon 1 of d-glucose Sickels, Jackson P.; Schultz, Harry P.
The pyranose forms of alpha- and beta-D-glucose, because of the cyclohexane conformations of their six-membered rings, do not explain the results of the conductivity of these sugars in boric acid.
Sickels, Jackson P.; Schultz, Harry P. J. Chem. Educ. 1964, 41, 343.
Molecular Properties / Structure |
Carbohydrates
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Ciphered formulas in carbohydrate chemistry Difini, Alvaro; Neto, Jose Difini
Describes the use of schematic formulas as an aid to rapidly representing configurations for monosaccharides.
Difini, Alvaro; Neto, Jose Difini J. Chem. Educ. 1958, 35, 38.
Carbohydrates |
Nomenclature / Units / Symbols |
Molecular Properties / Structure |
Chirality / Optical Activity
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Some difficulties and common errors related to the designation of sugar configurations Abernethy, John Leo
Examines some difficulties and common errors related to the designation of sugar configurations.
Abernethy, John Leo J. Chem. Educ. 1956, 33, 88.
Carbohydrates |
Nomenclature / Units / Symbols |
Molecular Properties / Structure |
Stereochemistry |
Chirality / Optical Activity |
Enantiomers
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A mnemonic for the monosaccharides Leary, R. H.
Presents a mnemonic for the D-series monosaccharides.
Leary, R. H. J. Chem. Educ. 1955, 32, 409.
Carbohydrates
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