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Klappentext This reference book aids chemical communication through the presentation of methods and their use in forming reasonable, acceptabel, and unambiguous names for organic compounds. It presents a common language for both sender and receiver in any context so that the nomenclature is made useful and understandable. The book is divided into two parts. The first is a general overview of organic nomenclature, the second uses concepts from the first part to answer the question "How do I name...?." Individual chapter are concerned with almost every class of organic derivative, stressing the relationship between structure and names. Zusammenfassung This reference book aids chemical communication through the presentation of methods and their use in forming reasonable, acceptabel, and unambiguous names for organic compounds. It presents a common language for both sender and receiver in any context so that the nomenclature is made useful and understandable. The book is divided into two parts. The first is a general overview of organic nomenclature, the second uses concepts from the first part to answer thequestion "How do I name...?". Individual chapter are concerned with almost every class of organic derivative, stressing th relationship between structure and names. INTRODUCTION; 1. Origin and Evolution of Organic Nomenclature; 2. Conventions in Organic Nomenclature; 3. Methods of Organic Nomenclature; 4. Common Errors, Pitfalls, and Misunderstandings; 5. Acyclic Hydrocarbons; 6. Alicyclic Hydrocarbons; 7. Arenes (Aromatic Hydrocarbons); 8. Hydrocarbon Ring Assemblies; 9. Heteroacyclic and Heterocyclic Compounds; 10. Groups Cited Only by Prefixes in Substitutive Nomenclature; 11. Carboxylic Acids, Acid Halides, and Replacement Analogs; 12. Carboxylic Esters, Slats, and Anhydrides; 13. Aldehydes and Their Chalcogen Analogs; 14. Ketones and Their Chalcogen Analogs; 15. Alcohols and Phenols; 16. Ethers; 17. Peroxides and Hydroperoxide; 18. Carboxylic Amides, Hydrazides, and Imides; 19. Amidines, and other Nitrogen Analogs or Amides; 20. Nitriles; 21. Amines and Imines; 22. Other Nitrogen Compounds; 23. Sulfur, Selemium, and Tellurium Acids, and Their Derivatives; 24. Thiols, Sulfides, Sulfoxides, and Sulfones, and Chalcogen Analogs; 25. Phosphorus and Arsenic Compounds; 26. Silicon, Germanium, Tin and Lead Compounds; 27. Organoboron Compounds; 28. Organometallic Compounds; 29. Polymers; 30. Steroisomers; 31. Natural Products; 32. Isotopically Modified Compounds; 33. Radicals, Ions, and Radical Ions; LIST OF TABLES...
