Click on the title of a resource to view it. To save screen space, only the first 3 resources are shown. You can display more resources by scrolling down and clicking on “View all xx results”. 1 Videos 26 Assessment Questions 113 Molecular Structures 11 Journal Articles 5 Other Resources Assessment Questions: First 3 results
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
Synthesis (11 Variations) A collection of 11 assessment questions about Synthesis Aldehydes / Ketones |
Synthesis |
Esters |
Oxidation / Reduction |
Alkynes |
Organometallics |
Alcohols |
Electrophilic Substitution
Alcohols and Ethers (22 Variations) A collection of 22 assessment questions about Alcohols and Ethers Alcohols |
Synthesis |
Oxidation / Reduction |
Aldehydes / Ketones |
Alkenes |
Carboxylic Acids |
Grignard Reagents |
Ethers |
Reactions |
Mechanisms of Reactions |
Organometallics |
Nomenclature / Units / Symbols |
Physical Properties
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Journal Articles: First 3 results.
Pedagogies:
Hands-On Learning / Manipulatives
Inquiry-Based / Discovery Learning
No Pedagogy
A Guided-Inquiry Approach to the Sodium Borohydride Reduction and Grignard Reaction of Carbonyl Compounds Robert E. Rosenberg Students teams identify unknowns and their reaction products and use their data to deduce that esters are less electrophilic than the other carbonyl compounds present, that Grignard reagents are more nucleophilic than sodium borohydride, and that carboxylic acid derivatives do not undergo the nucleophilic addition reactions that are characteristic of aldehydes and ketones. Rosenberg, Robert E. J. Chem. Educ. 2007, 84, 1474. Addition Reactions |
Aldehydes / Ketones |
Esters |
Grignard Reagents |
IR Spectroscopy |
Oxidation / Reduction |
Reactions |
Student-Centered Learning
Using a Premade Grignard Reagent To Synthesize Tertiary Alcohols in a Convenient Investigative Organic Laboratory Experiment Michael A. G. Berg and Roy D. Pointer Describes the use of a commercially available Grignard reagent in a Grignard synthesis that avoided the failures typically associated with the Grignard reaction. Berg, Michael A. G.; Pointer, Roy D. J. Chem. Educ. 2007, 84, 483. Aldehydes / Ketones |
Grignard Reagents |
IR Spectroscopy |
NMR Spectroscopy |
Organometallics |
Synthesis
Grubbs's Cross Metathesis of Eugenol with cis -2-Butene-1,4-diol To Make a Natural Product. An Organometallic Experiment for the Undergraduate Lab Douglass F. Taber and Kevin J. Frankowski Describes the ruthenium catalyzed cross metathesis of eugenol with cis-1,4-butenediol. The experiment is an excellent example of the powerful selectivity possible with the Grubbs' catalyst, demonstrating the preference for trans over cis alkene formation and for cross metathesis over homodimerization. Taber, Douglass F.; Frankowski, Kevin J. J. Chem. Educ. 2006, 83, 283. Alkenes |
Catalysis |
IR Spectroscopy |
Mass Spectrometry |
Mechanisms of Reactions |
Microscale Lab |
Natural Products |
NMR Spectroscopy |
Organometallics |
Stereochemistry |
Synthesis |
Thin Layer Chromatography |
Transition Elements
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Other Resources: First 3 results
Aldehydes and Ketones Ed Vitz, John W. Moore A section of ChemPrime, the Chemical Educations Digital Library's free General Chemistry textbook. Aldehydes / Ketones
Aldehydes and Ketones in the Cinnamon Trade Garrett Schwarzman A section of ChemPrime, the Chemical Educations Digital Library's free General Chemistry textbook. Aldehydes / Ketones
Ketosis in Biology Robert Hetue A section of ChemPrime, the Chemical Educations Digital Library's free General Chemistry textbook. Aldehydes / Ketones |
Metabolism |
Bioorganic Chemistry
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