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Author: Peter Wepplo Publisher: Curved Arrow Press ISBN: 0977931331 Category : Science Languages : en Pages : 158
Book Description
A Handbook to Organic Chemistry Mechanisms is designed to accompany a standard organic chemistry textbook. The book presents complete mechanisms, start to finish, without any steps skipped or left out. The mechanisms have been carefully written to show each step in a logical and easy to follow format. Students have enthusiastically attested to the ease with which they could understand the mechanisms. Reaction mechanisms are one of the most challenging aspects of organic chemistry. This book is derived from Part D of A Guide to Organic Chemistry Mechanisms. That book is a guided inquiry workbook that shows students how to study and enables them to learn reaction mechanisms. Student knowledge is increased step by step by completing mechanisms at easy, moderate, and textbook levels of difficulty. A Handbook to Organic Chemistry Mechanisms also relies on example-based teaching. Chemical reactions can be learned in context, the way infants learn. Learning reactions from rules is difficult when there are many exceptions. Substitution and elimination reactions are noteworthy due to the number of conditions that must be accounted for. With example-based teaching, you can deduce the importance that stereochemistry, structure, solvent, leaving group, charge, basicity, or nucleophilicity may have on a reaction. A Handbook to Organic Chemistry Mechanisms has been designed with the principle that our brains are pattern-matching machines. Therefore, an emphasis has been placed upon the patterns of reactions. Each chapter represents a basic mechanistic theme. That theme is repeated with the examples. Insightful explanations have been included with the mechanisms. This book will be a valuable resource for reviewing for an exam, solving problems, or studying for the MCAT.
Author: Peter Wepplo Publisher: Curved Arrow Press ISBN: 0977931331 Category : Science Languages : en Pages : 158
Book Description
A Handbook to Organic Chemistry Mechanisms is designed to accompany a standard organic chemistry textbook. The book presents complete mechanisms, start to finish, without any steps skipped or left out. The mechanisms have been carefully written to show each step in a logical and easy to follow format. Students have enthusiastically attested to the ease with which they could understand the mechanisms. Reaction mechanisms are one of the most challenging aspects of organic chemistry. This book is derived from Part D of A Guide to Organic Chemistry Mechanisms. That book is a guided inquiry workbook that shows students how to study and enables them to learn reaction mechanisms. Student knowledge is increased step by step by completing mechanisms at easy, moderate, and textbook levels of difficulty. A Handbook to Organic Chemistry Mechanisms also relies on example-based teaching. Chemical reactions can be learned in context, the way infants learn. Learning reactions from rules is difficult when there are many exceptions. Substitution and elimination reactions are noteworthy due to the number of conditions that must be accounted for. With example-based teaching, you can deduce the importance that stereochemistry, structure, solvent, leaving group, charge, basicity, or nucleophilicity may have on a reaction. A Handbook to Organic Chemistry Mechanisms has been designed with the principle that our brains are pattern-matching machines. Therefore, an emphasis has been placed upon the patterns of reactions. Each chapter represents a basic mechanistic theme. That theme is repeated with the examples. Insightful explanations have been included with the mechanisms. This book will be a valuable resource for reviewing for an exam, solving problems, or studying for the MCAT.
Author: Robert J. Ouellette Publisher: Academic Press ISBN: 0128128399 Category : Technology & Engineering Languages : en Pages : 1058
Book Description
Organic Chemistry: Structure, Mechanism, Synthesis, Second Edition, provides basic principles of this fascinating and challenging science, which lies at the interface of physical and biological sciences. Offering accessible language and engaging examples and illustrations, this valuable introduction for the in-depth chemistry course engages students and gives future and new scientists a new approach to understanding, rather than merely memorizing the key concepts underpinning this fundamental area. The book builds in a logical way from chemical bonding to resulting molecular structures, to the corresponding physical, chemical and biological properties of those molecules. The book explores how molecular structure determines reaction mechanisms, from the smallest to the largest molecules—which in turn determine strategies for organic synthesis. The book then describes the synthetic principles which extend to every aspect of synthesis, from drug design to the methods cells employ to synthesize the molecules of which they are made. These relationships form a continuous narrative throughout the book, in which principles logically evolve from one to the next, from the simplest to the most complex examples, with abundant connections between the theory and applications. Featuring in-book solutions and instructor PowerPoint slides, this Second Edition offers an updated and improved option for students in the two-semester course and for scientists who require a high quality introduction or refresher in the subject. - Offers improvements for the two-semester course sequence and valuable updates including two new chapters on lipids and nucleic acids - Features biochemistry and biological examples highlighted throughout the book, making the information relevant and engaging to readers of all backgrounds and interests - Includes a valuable and highly-praised chapter on organometallic chemistry not found in other standard references
Author: Barry Keith Carpenter Publisher: Wiley-Interscience ISBN: Category : Science Languages : en Pages : 280
Book Description
This practical handbook presents concise descriptions of the most commonly employed experimental techniques for studying reaction mechanisms in organic chemistry. For each technique, all necessary theoretical background is covered, and at least one example of its application--taken from the research literature--is described in detail.
Author: Reinhard Bruckner Publisher: Academic Press ISBN: 9780121381103 Category : Science Languages : en Pages : 308
Book Description
A best-selling mechanistic organic chemistry text in Germany, this text's translation into English fills a long-existing need for a modern, thorough and accessible treatment of reaction mechanisms for students of organic chemistry at the advanced undergraduate and graduate level. Knowledge of reaction mechanisms is essential to all applied areas of organic chemistry; this text fulfills that need by presenting the right material at the right level.
Author: Robert B. Grossman Publisher: Springer Science & Business Media ISBN: 0387954686 Category : Science Languages : en Pages : 371
Book Description
Intended for students of intermediate organic chemistry, this text shows how to write a reasonable mechanism for an organic chemical transformation. The discussion is organized by types of mechanisms and the conditions under which the reaction is executed, rather than by the overall reaction as is the case in most textbooks. Each chapter discusses common mechanistic pathways and suggests practical tips for drawing them. Worked problems are included in the discussion of each mechanism, and "common error alerts" are scattered throughout the text to warn readers about pitfalls and misconceptions that bedevil students. Each chapter is capped by a large problem set.
Author: Paul H. Scudder Publisher: John Wiley & Sons ISBN: 0470638044 Category : Science Languages : en Pages : 448
Book Description
Sets forth the analytical tools needed to solve key problems in organic chemistry With its acclaimed decision-based approach, Electron Flow in Organic Chemistry enables readers to develop the essential critical thinking skills needed to analyze and solve problems in organic chemistry, from the simple to complex. The author breaks down common mechanistic organic processes into their basic units to explain the core electron flow pathways that underlie these processes. Moreover, the text stresses the use of analytical tools such as flow charts, correlation matrices, and energy surfaces to enable readers new to organic chemistry to grasp the fundamentals at a much deeper level. This Second Edition of Electron Flow in Organic Chemistry has been thoroughly revised, reorganized, and streamlined in response to feedback from both students and instructors. Readers will find more flowcharts, correlation matrices, and algorithms that illustrate key decision-making processes step by step. There are new examples from the field of biochemistry, making the text more relevant to a broader range of readers in chemistry, biology, and medicine. This edition also offers three new chapters: Proton transfer and the principles of stability Important reaction archetypes Qualitative molecular orbital theory and pericyclic reactions The text's appendix features a variety of helpful tools, including a general bibliography, quick-reference charts and tables, pathway summaries, and a major decisions guide. With its emphasis on logical processes rather than memorization to solve mechanistic problems, this text gives readers a solid foundation to approach and solve any problem in organic chemistry.
Author: Richard B. Silverman Publisher: Elsevier ISBN: 0080513379 Category : Science Languages : en Pages : 650
Book Description
Standard medicinal chemistry courses and texts are organized by classes of drugs with an emphasis on descriptions of their biological and pharmacological effects. This book represents a new approach based on physical organic chemical principles and reaction mechanisms that allow the reader to extrapolate to many related classes of drug molecules. The Second Edition reflects the significant changes in the drug industry over the past decade, and includes chapter problems and other elements that make the book more useful for course instruction. - New edition includes new chapter problems and exercises to help students learn, plus extensive references and illustrations - Clearly presents an organic chemist's perspective of how drugs are designed and function, incorporating the extensive changes in the drug industry over the past ten years - Well-respected author has published over 200 articles, earned 21 patents, and invented a drug that is under consideration for commercialization
Author: Shu Kobayashi Publisher: John Wiley & Sons ISBN: 9783527301591 Category : Science Languages : en Pages : 354
Book Description
During the miners' strike in the 1980s, a worker is killed in the striking coalfields of Wales. Some months later, a government minister thought to be connected with the death is also shot. Lewis Redfern—once a radical but now a political analyst and journalist—pursues the sniper, a lonely hunt that leads him through an imbroglio of civil service leaks to a secret organization: a source of insurrection far more powerful than anyone could have suspected known as the Volunteers. In this fast-paced narrative of espionage and intrigue, Redfern, through his obsessive pursuit of justice, finally encounters the truth about himself as the novel discusses the conflict between moral choice and political loyalty.
Author: Michael B. Smith Publisher: John Wiley & Sons ISBN: 0470084944 Category : Science Languages : en Pages : 2379
Book Description
The Sixth Edition of a classic in organic chemistry continues its tradition of excellence Now in its sixth edition, March's Advanced Organic Chemistry remains the gold standard in organic chemistry. Throughout its six editions, students and chemists from around the world have relied on it as an essential resource for planning and executing synthetic reactions. The Sixth Edition brings the text completely current with the most recent organic reactions. In addition, the references have been updated to enable readers to find the latest primary and review literature with ease. New features include: More than 25,000 references to the literature to facilitate further research Revised mechanisms, where required, that explain concepts in clear modern terms Revisions and updates to each chapter to bring them all fully up to date with the latest reactions and discoveries A revised Appendix B to facilitate correlating chapter sections with synthetic transformations
Author: Peter Wepplo
Author: Peter Wepplo
Author: Robert J. Ouellette
Author: Barry Keith Carpenter
Author: Reinhard Bruckner
Author: Robert B. Grossman
Author: Paul H. Scudder
Author: Richard B. Silverman
Author: Shu Kobayashi
Author: Michael B. Smith
Author: Peter Sykes