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3 Videos
4 Assessment Questions
118 Molecular Structures
4 Journal Articles
13 Other Resources
Videos: 3 results
Sucrose Dehydration gives Sulfur Dioxide  
Sulfuric acid dehydrates sucrose forming carbon.
Carbohydrates |
Oxidation / Reduction |
Reactions
Benedict's Test for Reducing Sugars  
Tests for glucose, sucrose, and fructose.
Carbohydrates |
Oxidation / Reduction |
Qualitative Analysis
Formation of Carbon from Carbohydrate  
Sulfuric acid has a very high affinity for water. It is shown to dehydrate a carbohydrate (sucrose) forming carbon. Sulfuric acid is reduced to sulfur dioxide, which bleaches a rose petal. In a second experiment, the sulfur dioxide reduces purple permanganate to nearly colorless manganese(II).
Acids / Bases |
Carbohydrates |
Oxidation / Reduction |
Reactions
Assessment Questions: First 3 results
Biochemistry : Anomer (20 Variations)
Classify each of the following monosaccharides as the or anomer.
Carbohydrates
Biochemistry : Disaccharide (20 Variations)
Classify each of the following disaccharides as having an or glycosidic bond.
Carbohydrates
Biochemistry : Carbform (20 Variations)
Which of the following molecules could be a carbohydrate?
Carbohydrates
View all 4 results
Molecular Structures: First 3 results
d-altrose C6H12O6

3D Structure

Link to PubChem

Carbohydrates

d-glucose C6H12O6

3D Structure

Link to PubChem

Carbohydrates

D-glucitol C6H14O6

3D Structure

Link to PubChem

Alcohols |
Carbohydrates

View all 118 results
Journal Articles: First 3 results.
Pedagogies:
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
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
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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Other Resources: First 3 results
Simple Sugars  Ed Vitz, John W. Moore
A section of ChemPrime, the Chemical Educations Digital Library's free General Chemistry textbook.
Carbohydrates
Disaccharides  Ed Vitz, John W. Moore
A section of ChemPrime, the Chemical Educations Digital Library's free General Chemistry textbook.
Carbohydrates
Carbohydrates  Ed Vitz, John W. Moore
A section of ChemPrime, the Chemical Educations Digital Library's free General Chemistry textbook.
Carbohydrates
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