000			04053nam a22002177a 4500
003			CUTN
005			20171120173105.0
008			171120b xxu||||| |||| 00| 0 eng d
020			_a3439385998898
082			_a547 _bHEA
100			_aHeathcock, Clayton H.
245			_aIntroduction to Organic Chemistry
250			_a4th Ed.
260			_bMedtech ; _c2017.
300			_a1320 p. _bill. ; _c27 cm.
500			_aThe book contains 22 chapters. Each chapter has been written in such a manner that the student will grasp the concepts easily. The subject matter has been written in simple language with lucid style. We hope that this book will prove to be useful for the readers of Organic Chemistry.Before you begin your adventure in organic chemistry it is perhaps appropriate for you to take few minutes to plan your journey. Organic chemistry is alive and continuously being transformed by new concepts, new technologies, and new reactions. Any modern textbook has to provide the fundamentals in a sound and clear manner, and to give a glimpse of the frontier. This edition is motivated by the need to expand the coverage in a biochemical/biological direction, and to introduce certain significant new developments in approach. Organic chemistry is so broad and encompasses so much that those of us concerned with teaching the subject to new generations of students keep searching for the best way. This book is indebted to numerous teachers and students of organic chemistry for suggested improvements to make our text still better. The color introduced in this edition has been recognized as a significant aid to study and in emphasizing the location of the site of reaction. Experienced organic chemists view structures as a unified gestalt and see quickly where structural change has occurred in a reaction. The inexperienced student needs to search for such changes. The use of color helps by "spotlighting" where the action is. We have also used color to indicate the essential stoichiometry of many reactions, showing where specific atoms go in a manner resembling the use of isotopic labels. We have tried to use color as a pedagogic tool. A “photoessay” insert shows that the sparing use of multiple colors allows one to combine good pedagogy with the aesthetic aspects of organic chemistry. We have also introduced “Asides” at the end of each chapter to present particular topics in a different context that should intrigue students.
505			_a1. Introduction 2. Electronic Structure and Bonding 3. Organic Structures 4. Organic Reactions 5. Alkanes 6. Reactions of Alkanes 7. Stereoisomerism 8. Alkyl Halides and Organometallic Compounds 9. Nucleophilic Substitution 10. Alcohols and Ethers 11. Alkenes 12. Alkynes and Nitrites 13. Nuclear Magnetic Resonance Spectroscopy 14. Aldehydes and Ketones 15. Aldeydes and Ketones: Enols 16. Organic Synthesis 17. Infrared Spectroscopy 18. Carboxylic Acids 19. Derivatives of Carboxylic Acids 20. Conjugation 21. Benzene and the Aromatic Ring 22. Molecular Orbital Theory 23. Electrophilic Aromatic Substitution 24. Amines 25. Other Nitrogen Functions 26. Sulfur, Phosphorus, and Silicon Compounds 27. Difunctional Compounds 28. Carbohydrates 29. Amino Acids, Peptides, and Proteins 30. Aromatic Haldes, Phenols, Phenyl Ethers, and Quinones 31. Polycyclic Aromatic Hydrocarbons 32. Heterocyclic Compounds 33. Molecular Recognition: Nucleic Acids and Some Biological Catalysts 34. Mass Spectrometry 35. The Chemical Literature 36. Special Topics Appendix I Heats of Formation Appendix II Bond-Dissociation Energies Appendix III Average Bond Energies Appendix IV Proton Chemical Shifts Appendix V Proton Chemical shifts Appendix V Symbols and Abbreviations Index
700			_aStreitwieser, Andrew
700			_aKosower, Edward M.
942			_2ddc _cBOOKS
999			_c24005 _d24005