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For the textbook, chapter, and section you specified we found
84 Videos
74 Assessment Questions
716 Journal Articles
33 Other Resources
Videos: First 3 results
Combustion Reactions  
Combustion reactions of methane, hydrogen, hexane, and natural gas in chlorine are demonstrated.
Reactions
Organic Compounds  
An assortment of organic compounds are ignited under various conditions.
Reactions
Reactions: Chlorine  
Reactions and explosions involving chlorine are demonstrated.
Reactions
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Assessment Questions: First 3 results
Reactions : GeneralRxnType (10 Variations)
Identify each of the following statements as describing a combination, displacement, decomposition, or exchange reaction.
Reactions
Reactions : GeneralChemRxn (4 Variations)
In a balanced chemical equation

Check all that apply.


Reactions
Reactions : NanoPicOfProducts (14 Variations)
The diagram below is representative of a tiny portion of a reaction between ammonia and methane. Which of the diagrams below represents the product mixture?


NH3(g) + CH4(g)HCN(g) + 3H2(g)


Reactions
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Journal Articles: First 3 results.
Pedagogies:
Synthesis Explorer: A Chemical Reaction Tutorial System for Organic Synthesis Design and Mechanism Prediction  Jonathan H. Chen and Pierre Baldi
Synthesis Explorer is an interactive tutorial system for organic chemistry that enables students to learn chemical reactions in ways previously unrealized. Pedagogical experiments in undergraduate classes at UC Irvine indicate that the system can improve average student examination performance by ~10%.
Chen, Jonathan H.; Baldi, Pierre. J. Chem. Educ. 2008, 85, 1699.
Mechanisms of Reactions |
Reactions |
Synthesis
Experimental Design and Optimization: Application to a Grignard Reaction  Naoual Bouzidi and Christel Gozzi
This 5-week project, which systematically investigates optimizing the synthesis of benzyl-1-cyclopentan-1-ol, constitutes an initiation into research methodology and experimental design to prepare the student-engineer for an industry internship. Other pedagogical goals include experience in synthetic techniques, obtaining reproducible yields, and using quantitative analysis methods.
Bouzidi, Naoual; Gozzi, Christel. J. Chem. Educ. 2008, 85, 1544.
Addition Reactions |
Alcohols |
Aldehydes / Ketones |
Chemometrics |
Gas Chromatography |
Organometallics |
Synthesis
Saying What You Mean: Teaching Mechanisms in Organic Chemistry  J. Brent Friesen
Ways to maintain clarity and consistency when teaching reaction mechanisms in organic chemistry include the use of balanced reaction equations, avoiding the use of shortcut notations, including key electrons and bonds in structural representations, and distinguishing between covalent and ionic bonds.
Friesen, J. Brent. J. Chem. Educ. 2008, 85, 1515.
Learning Theories |
Mechanisms of Reactions |
Reactions
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Other Resources: First 3 results
The Chemistry of Coffee  William F. Coleman
The paper Our Everyday Cup of Coffee: The Chemistry behind Its Magic by Marino Petracco provides a hearty blend of molecules for this month. The author deals with coffee at a number of different levels ranging from the economic and social to the still perplexing questions of flavor and aroma. The associated molecules demonstrate a range of structural features that students will benefit from examining in three dimensions.
Bioorganic Chemistry
Molecular Model of Tubocurarine  William F. Coleman
Curare, the Karib name for the plant from which this molecule is derived, is used in traditional South American medicine and hunting because it is a muscle relaxant. The three papers by Brunsvold and Ostercamp (1, 2, 3) provide us with an abundance of candidates for Featured Molecules this month. All of the major compounds highlighted in the papers, and many of the intermediates in the synthetic schemes, have been added to our collection. Students should note the structural similarities of the various barbiturate species and of the steroid-based compounds, as well as the interesting proto-cage structure of curare. Careful examination of the conformation of the alkyl groups in various of the molecules, when looked at as Newman projections, should convince students that their expectations about staggering substituents on adjacent tetrahedral-like carbon atoms are met in the computations. However, they should also be aware that recent work casts some doubt on the traditional explanation for that staggering (1). Charged species are presented in the collection in ionic form, without counterions (those are given in the papers), and all species except curare and atricurium besylate (molecule 40 in the third paper) were optimized at either HF/631-G(d) or B3LYP/631-G(d). The latter two molecules were optimized using HF/STO-3.
Bioorganic Chemistry
ChemPaths 104 M Feb 14  John W. Moore
Today in Chem 104: * Lecture: Review for Exam I (email questions or topics for discussion during the review session to Prof. Moore by 9am today) * No assigned reading for today. * Exam I on Wednesday Feb 16: Covers material through Feb 11; Biomolecules tutorials, Molecular Structure, Aspirin, and Biodiesel Labs.
Bioorganic Chemistry
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