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Test Bank for Organic Chemistry Principles and Mechanisms, 2nd edition Joel Karty
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Test Bank for Organic Chemistry Principles and Mechanisms, 2nd edition, Joel Karty,
Test Bank for Organic Chemistry Principles and Mechanisms, 2nd edition, Joel Karty
Product details:
- ISBN-10 : 0393630749
- ISBN-13 : 978-0393630749
- Author: Joel Karty
Organic chemistry can overwhelm students and force them to fall back on memorization. But once they understand how to use mechanisms, they can solve just about any problem. With an organization by mechanism, students will understand more, and memorize less. The Second Edition of this groundbreaking text provides a fresh, but proven approach to get students confident using mechanisms.
Smartwork5 online homework supports learning by mirroring the text’s organization and pedagogy. Students use an intuitive drawing tool while receiving instant hints and answer-specific feedback, making practice more productive.
Table of Content
1. Atomic and Molecular Structure
Interchapter A Nomenclature: The Basic System for Naming Simple Organic Compounds: Alkanes, Haloalkanes, Nitroalkanes, Cycloalkanes, and Ethers
2. Three-Dimensional Geometry, Intermolecular Interactions, and Physical Properties
3. Orbital Interactions 1: Hybridization and Two-Center Molecular Orbitals
Interchapter B Naming Alkenes, Alkynes, and Benzene Derivatives
4. Isomerism 1: Conformational and Constitutional Isomers
5. Isomerism 2: Chirality, Enantiomers, and Diastereomers
Interchapter C Stereochemistry in Nomenclature: R and S Configurations about Asymmetric Carbons and Z and E Configurations about Double Bonds
6. The Proton Transfer Reaction: An Introduction to Mechanisms, Thermodynamics, and Charge Stability
7. An Overview of the Most Common Elementary Steps
Interchapter D Molecular Orbital Theory, Hyperconjugation, and Chemical Reactions
Interchapter E Naming Compounds with a Functional Group That Calls for a Suffix 1: Alcohols, Amines, Ketones, and Aldehydes
8. An Introduction to Multistep Mechanisms: SN1 and E1 Reactions and Their Comparisons to SN2 and E2 Reactions
Interchapter F Naming Compounds with a Functional Group That Calls for a Suffix 2: Carboxylic Acids and Their Derivatives
9. Nucleophilic Substitution and Elimination Reactions 1: Competition among SN2, SN1, E2, and E1 Reactions
10. Nucleophilic Substitution and Elimination Reactions 2: Reactions That Are Useful for Synthesis
11. Electrophilic Addition to Nonpolar π Bonds 1: Addition of a Brønsted Acid
12. Electrophilic Addition to Nonpolar π Bonds 2: Reactions Involving Cyclic Transition States
13. Organic Synthesis 1: Beginning Concepts
14. Orbital Interactions 2: Extended π Systems, Conjugation, and Aromaticity
15. Structure Determination 1: Ultraviolet-Visible and Infrared Spectroscopies
16. Structure Determination 2: Nuclear Magnetic Resonance Spectroscopy and Mass Spectrometry
17. Nucleophilic Addition to Polar π Bonds 1: Addition of Strong Nucleophiles
18. Nucleophilic Addition to Polar π Bonds 2: Weak Nucleophiles and Acid and Base Catalysis
19. Organic Synthesis 2: Intermediate Topics in Synthesis Design, and Useful Redox and Carbon-Carbon Bond-Formation Reactions
20. Nucleophilic Addition–Elimination Reactions 1: The General Mechanism Involving Strong Nucleophiles
21. Nucleophilic Addition–Elimination Reactions 2: Weak Nucleophiles
22. Aromatic Substitution 1: Electrophilic Aromatic Substitution on Benzene; Useful Accompanying Reactions
23. Aromatic Substitution 2: Reactions of Substituted Benzene and Other Rings
24. The Diels–Alder Reaction and Other Pericyclic Reactions
25. Reactions Involving Free Radicals
Interchapter G Fragmentation Pathways in Mass Spectrometry
26. Polymers
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