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For the textbook, chapter, and section you specified we found
1 Videos
27 Assessment Questions
113 Molecular Structures
15 Journal Articles
5 Other Resources
Videos: 1 results
Aldol Condensation Reactions  
Aldol condensation reactions are demonstrated.
Aldehydes / Ketones |
Reactions
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
View all 27 results
Molecular Structures: First 3 results
Carbon Monoxide CO

3D Structure

Link to PubChem

VSEPR Theory |
Gases |
Toxicology |
Atmospheric Chemistry |
Bioinorganic Chemistry |
Biosignaling |
Organometallics

Formaldehyde CH2O

3D Structure

Link to PubChem

Aldehydes / Ketones

1R-camphor C10H16O

3D Structure

Link to PubChem

Aldehydes / Ketones

View all 113 results
Journal Articles: First 3 results.
Pedagogies:
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
View all 15 articles
Other Resources: First 3 results
Molecular Models of Ruthenium(II) Organometallic Complexes  William F. Coleman
The featured molecules for this month come from the paper "Experiments in Thermodynamics and Kinetics of Phosphine Substitution in (p-Cymene)RuCl2(PR3)" by Ozerov, Moura, and Hoffman in which they study the reactions of a number of "piano stool" complexes of ruthenium(II). The synthesis of compound 2a offers students an alternative to the preparation of ferrocene if they are only preparing one metal-arene complex, and the use of the (p-cymene)RuCl2 dimer as a starting material introduces them to a compound that has become important for the synthesis of a number of ruthenium catalysts. Two structures are found for the dimer in the gas phase, one with the chlorides cis to one another and a more stable form with the chlorides trans. DFT calculations using the LanL2MB basis set and the B3LYP functional in Gaussian 03 (1) show the trans form to be about 90 kJ/mol more stable than the cis form. The structures of the trans form of the dimer and of compound 2a are presented in 2 formats with bonds from the ruthenium ion to all of the carbons in the aryl ring and with a single line to a ghost atom in the center of the ring. These are the two common ways of representing such structures but students should be made aware that the overall coordination about the ruthenium in both the dimer and in compound 2a is octahedral, and should look at the structures to convince themselves of that fact. It is also instructive to look at compound 2a, and the other piano stool complexes that are made in the paper, to see how deceptive representation of the triphenylphosphine moiety as PR3 is in terms of the stereochemical bulk of that group.
Organometallics
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
View all 5 results