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For the textbook, chapter, and section you specified we found
6 Videos
2 Assessment Questions
81 Molecular Structures
8 Journal Articles
2 Other Resources
Videos: First 3 results
Addition Reactions of Alkenes  
The Diels-Alder reaction, addition of oxygen to tetrakis(N, N-dimethylamino) ethylene, polymerization of ethylene, and addition of iodine to a-pinene are demonstrated. Molecular models of ethene are shown.
Addition Reactions |
Alkenes
Diels-Alder Visualization  
Several computer animations of a Diels-Alder reaction that were created as an undergraduate student project are presented.
Addition Reactions |
Alkenes
Reactions of Iodine with alpha-Pinene  
Reactions of Iodine with alpha-Pinene
Addition Reactions |
Alkenes |
Applications of Chemistry
View all 6 results
Assessment Questions: 2 results
Organic : CisTransPossible (20 Variations)
Which of the following molecules can have cis and trans isomers? (You may select more than one.)
Alkenes |
Stereochemistry
Organic : FindIdenticalIsomers (20 Variations)
Which of the following structural isomers for C6H14 are actually the same structure?
Alkanes / Cycloalkanes |
Alkenes |
Constitutional Isomers
Molecular Structures: First 3 results
Ethylene CH2CH2

3D Structure

Link to PubChem

Alkenes

1R-camphene C10H16

3D Structure

Link to PubChem

Alkenes

2-methylbut-2-ene C5H10

3D Structure

Link to PubChem

Alkenes

View all 81 results
Journal Articles: First 3 results.
Pedagogies:
A Sequence of Linked Experiments, Suitable for Practical Courses of Inorganic, Organic, Computational Chemistry, and NMR Spectroscopy  Grigoriy A. Sereda
A sequence of investigations associated with the iodochlorination of styrene and 1-hexene is described. The sequence is flexible enough to be used in inorganic, organic, computational, and instrumental courses.
Sereda, Grigoriy A. J. Chem. Educ. 2006, 83, 931.
Alkenes |
Computational Chemistry |
Constitutional Isomers |
MO Theory |
NMR Spectroscopy |
Synthesis
"You're Repulsive!"Teaching VSEPR in a Not-So-Elegant Way  Robert S. H. Liu
Valence shell electron pair repulsive (VSEPR) interaction is an important concept particularly in discussing structural properties of molecules. In this article we showed five organic examples not commonly associated with VSEPR but yet all involving repulsive interactions of valence electrons, which provides ready explanations for altered chemical reactivity and spectroscopic properties of organic compounds. The ready catchy phrase Youre Repulsive! is the common thread used throughout these five examples.
Liu, Robert S. H. J. Chem. Educ. 2005, 82, 558.
Mechanisms of Reactions |
UV-Vis Spectroscopy |
Reactions |
Addition Reactions |
Electrophilic Substitution
The Evolution of a Green Chemistry Laboratory Experiment: Greener Brominations of Stilbene  Lallie C. McKenzie, Lauren M. Huffman, and James E. Hutchison
We describe two new greener alkene bromination reactions that offer enhanced laboratory safety and convey important green chemistry concepts, in addition to illustrating the chemistry of alkenes. The two alternative reactions, one involving pyridinium tribromide and a second using hydrogen peroxide and hydrobromic acid, are compared to the traditional bromination of stilbene through the application of green metrics, including atom economy, percent experimental atom economy, E factor, and effective mass yield.
McKenzie, Lallie C.; Huffman, Lauren M.; Hutchison, James E. J. Chem. Educ. 2005, 82, 306.
Synthesis |
Green Chemistry |
Aromatic Compounds |
Addition Reactions |
Alkenes
View all 8 articles
Other Resources: 2 results
Alcohols  Ed Vitz, John W. Moore
A section of ChemPrime, the Chemical Educations Digital Library's free General Chemistry textbook.
Alcohols |
Addition Reactions
Unsaturated Hydrocarbons  Ed Vitz, John W. Moore
A section of ChemPrime, the Chemical Educations Digital Library's free General Chemistry textbook.
Alkenes |
Alkynes