Physical organic chemistry is a modern scientific subdiscipline whose reach is pervasive throughout chemistry, underpinning every academic and industrial synthetic process. In Thinking Like a Physical Organic Chemist, Professor Steven M. Bachrach uses analogies and colorful examples to provide experts and nonexperts alike with an alternative way of thinking about organic chemistry. He highlights a number of reaction mechanisms, walking through the important experiments that they rest upon, with an emphasis on the rules and logic systems that organic chemists have built to understand and predict reaction outcomes.…mehr
Physical organic chemistry is a modern scientific subdiscipline whose reach is pervasive throughout chemistry, underpinning every academic and industrial synthetic process. In Thinking Like a Physical Organic Chemist, Professor Steven M. Bachrach uses analogies and colorful examples to provide experts and nonexperts alike with an alternative way of thinking about organic chemistry. He highlights a number of reaction mechanisms, walking through the important experiments that they rest upon, with an emphasis on the rules and logic systems that organic chemists have built to understand and predict reaction outcomes.Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Steven M. Bachrach is Dean of the Artis College of Science and Technology at Radford University. Previously, Bachrach was Dean of the School of Science at Monmouth University, and the Dr. D. R. Semmes Distinguished Professor of Chemistry at Trinity University. He has published more than 130 articles and is the author of Computational Organic Chemistry. He was a pioneer in exploring the use of the Internet for chemical publication. The National Science Foundation, the Welch Foundation, and the Dreyfus Foundation have supported his research. He lives in Virginia, USA.
Inhaltsangabe
Preface Chapter 1. Itineraries Chapter 2. Chemistry Basics Chapter 3. Tour de France Stages Chapter 4. Potential Energy Surface (PES) Features Chapter 5. Nucleophilic Substitution Reactions. I. Basics and SN1 Chapter 6. Nucleophilic Substitution Reactions. II. SN2 Chapter 7. Nucleophilic Substitution Reactions. III. Stereochemistry Chapter 8. Interlude: Philosophy of Science Chapter 9. Nucleophilic Substitution Reactions. IV. Further Details Chapter 10. Elimination Reactions. I. E1 and E2 Chapter 11. Elimination Reactions. II. Conformation and Stereochemistry Chapter 12: The Truth about Substitution and Elimination Reactions Chapter 13. More Hard Truths: Alkyls as Electron Donating Groups Chapter 14. Addition Reactions: Kinetic and Thermodynamic Control Chapter 15. Quantum Mechanical Tunneling Chapter 16. Aromaticity Chapter 17. Pericyclic Reactions Chapter 18. Reaction Dynamics Chapter 19. Lessons Learned Acknowledgments Bibliography
Preface Chapter 1. Itineraries Chapter 2. Chemistry Basics Chapter 3. Tour de France Stages Chapter 4. Potential Energy Surface (PES) Features Chapter 5. Nucleophilic Substitution Reactions. I. Basics and SN1 Chapter 6. Nucleophilic Substitution Reactions. II. SN2 Chapter 7. Nucleophilic Substitution Reactions. III. Stereochemistry Chapter 8. Interlude: Philosophy of Science Chapter 9. Nucleophilic Substitution Reactions. IV. Further Details Chapter 10. Elimination Reactions. I. E1 and E2 Chapter 11. Elimination Reactions. II. Conformation and Stereochemistry Chapter 12: The Truth about Substitution and Elimination Reactions Chapter 13. More Hard Truths: Alkyls as Electron Donating Groups Chapter 14. Addition Reactions: Kinetic and Thermodynamic Control Chapter 15. Quantum Mechanical Tunneling Chapter 16. Aromaticity Chapter 17. Pericyclic Reactions Chapter 18. Reaction Dynamics Chapter 19. Lessons Learned Acknowledgments Bibliography
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