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For the textbook, chapter, and section you specified we found
5 Assessment Questions
63 Journal Articles
Assessment Questions: First 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
Alkanes (22 Variations)
A collection of 22 assessment questions about Alkanes
Alkanes / Cycloalkanes |
Conformational Analysis |
Nomenclature / Units / Symbols |
Lewis Structures |
Stereochemistry |
Reactions
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
View all 5 results
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
A-DNA and B-DNA: Comparing Their Historical X-ray Fiber Diffraction Images  Amand A. Lucas
This paper provides a comparative explanation of the structural content of the diffraction diagrams of A-DNA and B-DNA that facilitated the discovery of the double-helical structure of DNA by Watson and Crick in 1953. This analysis is supported a method that simulates both A-DNA and B-DNA X-ray images optically.
Lucas, Amand A. J. Chem. Educ. 2008, 85, 737.
Biophysical Chemistry |
Conformational Analysis |
Crystals / Crystallography |
X-ray Crystallography |
Nucleic Acids / DNA / RNA
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
View all 63 articles