Test Bank for Organic Chemistry Mechanistic Patterns 1st Edition by Ogilvie

Product details:

• ISBN-10 ‏ : ‎ 017650026X
• ISBN-13 ‏ : ‎ 978-0176500269
• Author: William Ogilvie

Organic Chemistry: Mechanistic Patterns is the very first introductory organic chemistry title that holistically focuses on a mechanistic approach; an approach that has proven to achieve a deeper understanding of chemical reactivity. This mechanistic approach to the dynamic world of organic chemistry visualizes reactivity as a collection of patterns in electron movement, making it possible for students to describe why a reaction occurred. Recognizing patterns of electron flow between seemingly different reactions can allow students to predict how a chemical will react, even if they have never seen a particular reaction before. The text takes great care to establish a progression of reactivity, from simple to complex, introducing functional groups as necessary, while focusing on the reaction at hand rather than the various things that each functional group does. Together, we seek to open students’ eyes to the dynamic world of organic chemistry with a more powerful and systematic approach to learning.

Table contents:

1. CHAPTER 1 Carbon and Its Compounds
2. CHAPTER 2 Anatomy of an Organic Molecule
3. CHAPTER 3 Molecules in Motion: Conformations by Rotations
4. CHAPTER 4 Stereochemistry: Three-Dimensional Structure in Molecules
5. CHAPTER 5 Organic Reaction Mechanism: Using Curved Arrows to Analyze Reaction Mechanisms
6. CHAPTER 6 Acids and Bases
7. CHAPTER 7 π Bonds as Electrophiles: Reactions of Carbonyls and Related Functional Groups
8. CHAPTER 8 π Bonds as Nucleophiles: Reactions of Alkenes, Alkynes, Dienes, and Enols
9. CHAPTER 9 Conjugation and Aromaticity
10. CHAPTER 10 Synthesis Using Aromatic Materials: Electrophilic Aromatic Substitution and Directed Orth
11. CHAPTER 11 Displacement Reactions on Saturated Carbons: SN1 and SN2 Substitution Reactions
12. CHAPTER 12 Formation of π Bonds by Elimination Processes: Elimination and Oxidation Reactions
13. CHAPTER 13 Structure Determination I: Nuclear Magnetic Resonance Spectroscopy
14. CHAPTER 14 Structure Determination II: Mass Spectrometry and Infrared Spectroscopy
15. CHAPTER 15 π Bond Electrophiles Connected to Leaving Groups: Carboxylic Acid Derivatives
16. CHAPTER 16 π Bonds with Hidden Leaving Groups: Reactions of Acetals and Related Compounds
17. CHAPTER 17 Carbonyl-Based Nucleophiles: Aldol, Claisen, Wittig, and Related Enolate Reactions
18. CHAPTER 18 Selectivity and Reactivity in Enolate Reactions: Control of Stereoselectivity and
19. CHAPTER 19 Radicals: Halogenation, Polymerization, and Reduction Reactions
20. CHAPTER 20 Reactions Controlled by Orbital Interactions: Ring Closures, Cycloadditions, and Rearrang
21. Appendix A Answers to Checkpoint Problems
22. Appendix B Common Errors in Organic Structures and Mechanisms
23. Appendix C pKa Values of Selected Organic Compounds
24. Appendix D NMR and IR Spectroscopic Data
25. Appendix E Periodic Table of the Elements
26. GLOSSARY
27. INDEX

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