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For the textbook, chapter, and section you specified we found
3 Videos
12 Assessment Questions
2 Molecular Structures
123 Journal Articles
2 Other Resources
Videos: 3 results
Chirality  
A series of chiral and achiral objects, the interaction of polarized light with organic molecules, the assignment of R- and S- configuration, Fisher projections, and a stereospecific reaction are demonstrated.
Chirality / Optical Activity |
Stereochemistry
Glyceraldehyde and the Fischer Projection  
Molecular models are used to demonstrate chirality of glyceraldehyde and drawing its Fischer Projection.
Chirality / Optical Activity |
Stereochemistry |
Molecular Properties / Structure
Structures and Conformations  
Molecular models are used to demonstrate the conformations of alkanes and cycloalkanes.
Alkanes / Cycloalkanes |
Molecular Properties / Structure |
Nomenclature / Units / Symbols |
Stereochemistry
Assessment Questions: First 3 results
Organic : CisTransPossible (20 Variations)
Which of the following molecules can have cis and trans isomers? (You may select more than one.)
Alkenes |
Stereochemistry
Alpha Beta Unsaturated Ketones and Aldehydes (13 Variations)
A collection of 13 assessment questions about Alpha Beta Unsaturated Ketones and Aldehydes
Aldehydes / Ketones |
Organometallics |
Stereochemistry |
Esters
Alkylation (6 Variations)
A collection of 6 assessment questions about Alkylation
Aldehydes / Ketones |
Alkylation |
Stereochemistry |
Diastereomers |
Enantiomers
View all 12 results
Molecular Structures: 2 results
Dinitrogen Difluoride (E) N2F2(E)

3D Structure

Link to PubChem

Molecular Properties / Structure |
Stereochemistry |
Nonmetals

Dinitrogen Difluoride (Z) N2F2(Z)

3D Structure

Link to PubChem

Molecular Properties / Structure |
Stereochemistry |
Nonmetals

Journal Articles: First 3 results.
Pedagogies:
The Synthesis of N-Benzyl-2-azanorbornene via Aqueous Hetero Diels–Alder Reaction  Xavier Sauvage and Lionel Delaude
Characterization of the product of this organic synthesis through IR and NMR data analysis provides valuable material to familiarize students with different types of protonproton coupling patterns and their typical ranges, serves to illustrate the concepts of green chemistry and atom efficiency, and can be used to exemplify structural analysis and computational studies.
Sauvage, Xavier; Delaude, Lionel. J. Chem. Educ. 2008, 85, 1538.
Alkenes |
Aqueous Solution Chemistry |
Conformational Analysis |
Green Chemistry |
IR Spectroscopy |
Molecular Modeling |
NMR Spectroscopy |
Stereochemistry |
Synthesis
Borohydride Reduction of Estrone  Animesh Aditya, David E. Nichols, and G. Marc Loudon
This experiment presents a guided-inquiry approach to the demonstration of diastereoselectivity using chiral hindered ketones that undergo facile reduction with sodium borohydride. The resulting diastereomeric estradiols can be analyzed and differentiated by thin-layer chromatography and melting point.
Aditya, Animesh; Nichols, David E.; Loudon, G. Marc. J. Chem. Educ. 2008, 85, 1535.
Aldehydes / Ketones |
Diastereomers |
IR Spectroscopy |
Microscale Lab |
Stereochemistry |
Steroids |
Thin Layer Chromatography
The Same and Not the Same: Chirality, Topicity, and Memory of Chirality  Wolfgang H. Kramer and Axel G. Griesbeck
Describes a simple molecular approach that aids students in learning stereochemical terms, definitions, and concepts, particularly when chemical structures are drawn in two dimensions.
Kramer, Wolfgang H.; Griesbeck, Axel G. J. Chem. Educ. 2008, 85, 701.
Chirality / Optical Activity |
Stereochemistry
View all 123 articles
Other Resources: 2 results
Stereochemistry Tutorial  Nicola Burrmann
Master the concepts organic stereochemistry with this interactive tutorial. It includes definitions, different three dimensional representations, assigning priorities to stereocenters, and determining the stereochemical relationship between molecules. Each section is followed by a question set that tests knowledge and understanding.
Stereochemistry |
Chirality / Optical Activity
Mage; A Tool for Developing Interactive Instructional Graphics  Stephen F. Pavkovic
Mage is a graphics program especially well suited for visualizing three-dimensional structures of proteins and other macromolecules. It is an important tool for biochemists and finds many applications in biochemistry courses. We utilize Mage to create interactive instructional graphics of potential use in a wider range of undergraduate chemistry courses, and present some of those applications here.
Crystals / Crystallography |
Group Theory / Symmetry |
VSEPR Theory |
Molecular Properties / Structure |
Stereochemistry |
Proteins / Peptides