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For the textbook, chapter, and section you specified we found
1 Videos
3 Assessment Questions
17 Journal Articles
Videos: 1 results
Nucleophilic Substitution Reactions  
Solvolysis of secondary versus tertiary halides, effects of leaving groups, solvolysis of/and reactions of sodium iodide and silver nitrate with isomers of bromobutane, SN1 and SN2 mechanisms, and hydrolysis of tert-butyl chloride are demonstrated.
Nucleophilic Substitution
Assessment Questions: 3 results
Substitution and Elimination (6 Variations)
A collection of 6 assessment questions about Substitution and Elimination
Mechanisms of Reactions |
Nucleophilic Substitution |
Elimination Reactions |
Carbocations |
Stereochemistry |
Alcohols |
Ethers
Nucleophilic Substitution (18 Variations)
A collection of 18 assessment questions about Nucleophilic Substitution
Nucleophilic Substitution |
Carbocations |
Alcohols |
Stereochemistry |
Epoxides |
Ethers
Aldol Reactions (30 Variations)
A collection of 30 assessment questions about Aldol Reactions
Aldehydes / Ketones |
Esters |
Amides |
Carboxylic Acids |
Mechanisms of Reactions |
Acids / Bases |
Reactions |
Synthesis |
Elimination Reactions |
Resonance Theory
Journal Articles: First 3 results.
Pedagogies:
Pyrolysis of Aryl Sulfonate Esters in the Absence of Solvent: E1 or E2? A Puzzle for the Organic Laboratory  John J. Nash, Marnie A. Leininger, and Kurt Keyes
An aryl sulfonate ester is synthesized and then pyrolyzed at reduced pressure. The volatile products are analyzed using gas chromatography to determine whether the thermal decomposition occurs via an E1 or E2 mechanism.
Nash, John J.; Leininger, Marnie A.; Keyes, Kurt . J. Chem. Educ. 2008, 85, 552.
Alkenes |
Carbocations |
Elimination Reactions |
Gas Chromatography |
Mechanisms of Reactions |
Synthesis
A Discovery-Based Experiment Involving Rearrangement in the Conversion of Alcohols to Alkyl Halides  Richard A. Kjonaas and Ryand J. F. Tucker
This article reports a discovery-based experiment in which students convert three alcohols to alkyl halides under acidic conditions and record the 13C NMR spectrum in each case. By comparing the number of resonances observed with the number of resonances predicted for each possible product, students draw several conclusions about the resulting rearrangement.
Kjonaas, Richard A.; Tucker, Ryand J. F. J. Chem. Educ. 2008, 85, 100.
Alcohols |
Carbocations |
Gas Chromatography |
NMR Spectroscopy |
Nucleophilic Substitution
Semiempirical and DFT Investigations of the Dissociation of Alkyl Halides  Jack R. Waas
Enthalpy changes corresponding to the gas phase heats of dissociation of 12 organic halides were calculated using two semiempirical methods, the HartreeFock method, and two DFT methods. All five methods agreed generally with the expected empirically known trends in the dissociation of alkyl halides.
Waas, Jack R. J. Chem. Educ. 2006, 83, 1017.
Alkanes / Cycloalkanes |
Computational Chemistry |
Mechanisms of Reactions |
Molecular Modeling |
Reactions |
Reactive Intermediates |
Thermodynamics |
Elimination Reactions |
Nucleophilic Substitution
View all 17 articles