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020			_a9789385998898
037			_cTextual
040			_beng _cCSL
041			_aeng
100			_aHeathcock, Clayton H. _9851880
245		0	_aClayton's introduction to organic chemistry
250			_a4th
260			_aNew Delhi, _bMedtech: _c2017.
300			_axviii, 1256p. _b: ill.
500			_aAppendix I-VI 1-11p.; Index 1-32p.
520			_aBefore 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. The 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.
650			_a Alkenes _9851881
650			_a Carboxylic acids _9851882
650			_a Conjugation _9851883
650			_a Nucleophilic substitution _9851884
650			_aStereoisomerism _9851885
700			_aKosower, Edward M. _9851886
700			_aHeathcock, Clayton H. _9851880
700			_aStreitwieser, Andrew _9851887
942			_hE5 L6;Q7-;1 _cTB _2CC _n0
999			_c2641 _d2641