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Brand New, Unread Copy in Perfect Condition. A+ Customer Service! Summary: 1. What is organic chemistry? 2. Organic structures 3. Determining organic structures 4. Structure of molecules 5. Organic reactions 6. Nucleophilic addition to the carbonyl group 7. Delocalization and conjugation 8. Acidity, basicity, and pKa 9. Using organometallic reagents to make C-C bonds 10. Conjugate addition 11. Proton nuclear magnetic resonance 12. Nucleophilic substitution at the carbonyl (C=O) group 13. Equilibria, rates, and mechanisms: summary of mechanistic principles 14. Nucleophilic substitution at C=O with loss of carbonyl oxygen 15. Review of spectroscopic methods 16. Stereochemistry 17. Nucleophilic substitution at saturated carbon 18. Conformational analysis 19. Elimination reactions 20. Electrophilic addition to alkenes 21. Formation and reactions of enols and enolates 22. Electrophilic aromatic substitution 23. Electrophilic alkenes 24. Chemoselectivity: selective reactions and protection 25. Synthesis in action 26. Alkylation of enolates 27. Reactions of enolates with aldehydes and ketones: the aldol reaction 28. Acylation at carbon 29. Conjugate addition of enolates 30. Retrosynthetic analysis 31. Controlling the geometry of double bonds 32. Determination of stereochemistry by spectroscopic methods 33. Stereoselective reactions of cyclic compounds 34. Diastereoselectivity 35. Pericyclic reactions 1: cycloadditions 36. Pericyclic reactions 2: sigmatropic and electrocyclic reactions 37. Rearrangements 38. Fragmentation 39. Radical reactions 40. Synthesis and reactions of carbenes 41. Determining reaction mechanisms 42. Saturated heterocycles and stereoelectronics 43. Aromatic heterocycles 1: structures and reactions 44. Aromatic heterocycles 2: synthesis 45. Asymmetric synthesis 46. Organo-main-group chemistry I: sulfur 47. Organo-main-group chemistry II: boron, silicon, and tin 48. Organometallic chemistry 49. The chemistry of life 50. Mechanisms in biological chemistry 51. Natural products 52. Polymerization 53. Organic chemistry today Index. Bookseller Inventory #

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Synopsis: This new and innovative text helps students develop a deeper understanding of organic chemistry. It treats the subject as a coherent whole, complete with numerous logical connections, consequences, and an underlying structure and "language." Employing an approach based on mechanism and reaction type, the book empasizes understanding ideas rather than merely memorizing facts. It shows students how to realistically draw molecules and mechanisms to reveal the fundamental chemistry.

Using a fresh, accessible writing style as well as examples from everyday life, the authors explain the basics of organic chemistry carefully and thoroughly. A special focus on mechanism, orbitals, and stereochemistry helps students gain a solid comprehension of important factors common to all reactions. The book's innovative design enhances clarity and instruction with boxes that separate summary information and other material from the main text; a variety of colors that draw attention to items such as atoms, molecules, and orbitals; and figures that are drawn in red with significant parts emphasized in black. Early chapters feature carbonyl group reactions, and later chapters systematically develop the chemistry through discussions of spectroscopy, stereochemistry, and chemical reactions.

Each chapter opens with a "Connections" box, divided into three columns:
· Building on: Details material from previous chapters that relate to the current chapter
· Arriving at: Provides a guide to the content of the chapter
· Looking forward to: Previews later chapters, which develop and expand the current material

About the Author: Jonathan Clayden is at University of Manchester. Nick Greeves is at University of Liverpool.

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