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1 Videos
1 Assessment Questions
230 Molecular Structures
43 Journal Articles
Videos: 1 results
Structure-Property Relations for Alkanes and Alcohols  
Boiling points of alkanes, miscibility of alcohols, and the vapor pressure and viscosity of several organic compounds are demonstrated.
Alkanes / Cycloalkanes |
Physical Properties |
Alcohols
Assessment Questions: 1 results
Organic : FunctionalGroups (18 Variations)
The structure for niacin (one of the B-vitamins) is shown below. Which of the following functional groups is present in niacin?

Alcohols |
Aldehydes / Ketones |
Carboxylic Acids |
Esters |
Amines / Ammonium Compounds
Molecular Structures: First 3 results
Methanol CH3OH

3D Structure

Link to PubChem

Alcohols

1_1_1_3_3_3-hexafluoropropan-2-ol C3H2F6O

3D Structure

Link to PubChem

Alcohols

butan-1-ol C4H10O

3D Structure

Link to PubChem

Alcohols

View all 230 results
Journal Articles: First 3 results.
Pedagogies:
The Comparative Nucleophilicity of Naphthoxide Derivatives in Reactions with a Fast-Red TR Dye  Cheryl M. Mascarenhas
In this experiment, organic chemistry students perform reactions between three naphthyl acetate derivatives and the diazonium salt Fast-Red TR. Students discover under what conditions the hydrolysis and electrophilic aromatic substitution is fastest and slowest, allowing them to conclude that latter, rather than the former, is rate-limiting.
Mascarenhas, Cheryl M. J. Chem. Educ. 2008, 85, 1271.
Alcohols |
Aromatic Compounds |
Dyes / Pigments |
Esters |
IR Spectroscopy |
NMR Spectroscopy |
Synthesis |
Thin Layer Chromatography |
UV-Vis Spectroscopy
Synthesis and Characterization of 9-Hydroxyphenalenone Using 2D NMR Techniques  Benjamin Caes and Dell Jensen Jr.
The synthesis of 9-Hydroxyphenalenone produces a planar multicyclic beta-ketoenol, the tautomerization of which results in C2v symmetry on the NMR time scale, thus simplifying the spectra and providing a unique structure for teaching 2D NMR spectroscopy.
Caes, Benjamin; Jensen, Dell, Jr. J. Chem. Educ. 2008, 85, 413.
Alcohols |
Aldehydes / Ketones |
Aromatic Compounds |
IR Spectroscopy |
NMR Spectroscopy |
Synthesis
Regioselectivity in Organic Synthesis: Preparation of the Bromohydrin of α-Methylstyrene  Brad Andersh, Kathryn N. Kilby, Meghan E. Turnis, and Drew L. Murphy
In the described experiment, the regiochemical outcome of the addition of "HOBr" to a-methylstyrene is investigated. Although both "classic" qualitative analysis and instrumental techniques are described, the emphasis of this experiment is on the utilization 13C and DEPT-135 NMR spectroscopy to determine the regiochemical outcome of the addition.
Andersh, Brad; Kilby, Kathryn N.; Turnis, Meghan E.; Murphy, Drew L. J. Chem. Educ. 2008, 85, 102.
Addition Reactions |
Alcohols |
Alkenes |
Constitutional Isomers |
IR Spectroscopy |
Microscale Lab |
NMR Spectroscopy |
Synthesis
View all 43 articles