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Item specifics

Condition
Good: A book that has been read, but is in good condition. Minimal damage to the book cover eg. ...
ISBN
0198503466
EAN
9780198503460
Date of Publication
2000-07-20
Release Title
Organic Chemistry
Artist
Wothers, Peter
Brand
N/A
Colour
N/A
Book Title
Organic Chemistry

About this product

Product Identifiers

Publisher
Oxford University Press, Incorporated
ISBN-10
0198503466
ISBN-13
9780198503460
eBay Product ID (ePID)
1745152

Product Key Features

Number of Pages
1536 Pages
Language
English
Publication Name
Organic Chemistry
Subject
Chemistry / Organic
Publication Year
2000
Type
Textbook
Subject Area
Science
Author
Jonathan Clayden, Nick Greeves, Stuart Warren, Peter Wothers
Format
Trade Paperback

Dimensions

Item Height
2.3 in
Item Weight
116.4 Oz
Item Length
10.9 in
Item Width
8.6 in

Additional Product Features

Intended Audience
College Audience
LCCN
2001-274062
Reviews
'"The book is brillant - we have been waiting for upto 25 years for adecent British text".'John Mann, Professor of Biol. Chemistry, Queens University Belfast, '"The book is brilliant - we have been waiting for up to 25 years for a decent British text".'John Mann, Professor of Biol. Chemistry, Queens University Belfast, '"The book gives a comprehensive overview of undergraduate-level organic chemistry and is suitable for all 3 years of a BSc degree. The writing and illustrations are very clear and easy".' Dr J G Knight, Lecturer, Newcastle University, What strikes the reader straight away is the way the text is laid out so that it is visually exciting. ...I could go on, so let me end by congratulating the authors and publishers in producing what I am sure will become the standard text in organic chemistry. Perhaps I should just summarise how I felt about the book when I came to put it down: refreshing, exciting and motivational. Tony Barrett, Imperial College London, '"The book is brilliant - we have been waiting for up to 25 years for adecent British text".'John Mann, Professor of Biol. Chemistry, Queens University Belfast, '"This is a book we have all been waiting for! It is based on soundmechanistic reasoning and contains thousands of useful examples for teaching.Its style is approachable and covers both fundamental and more advancedmaterial".'Adam Nelson, Lecturer, University of Leeds, "It is veru useful, and it is very different from other student books. Ithink it is clearly written..." Organische- Chemie., '"It is a very modern book showing nicely the interaction between organicchemistry and daily life. It has an unusaul and exciting format".'Frank-Gerrit Klarner, Prof. Dr., Universitat Essen, '"The book gives a comprehensive overview of undergraduate-level organicchemistry and is suitable for all 3 years of a BSc degree. The writing andillustrations are very clear and easy".'Dr J G Knight, Lecturer, Newcastle University, "It is veru useful, and it is very different from other student books. I think it is clearly written..." Organische- Chemie., '"It is a very modern book showing nicely the interaction between organic chemistry and daily life. It has an unusaul and exciting format".' Frank-Gerrit Klarner, Prof. Dr., Universitat Essen, '"This is a book we have all been waiting for! It is based on sound mechanistic reasoning and contains thousands of useful examples for teaching. Its style is approachable and covers both fundamental and more advanced material".'Adam Nelson, Lecturer, University of Leeds
Dewey Edition
21
Illustrated
Yes
Dewey Decimal
547
Table Of Content
1. What is organic chemistry?2. Organic structures3. Determining organic structures4. Structure of molecules5. Organic reactions6. Nucleophilic addition to the carbonyl group7. Delocalization and conjugation8. Acidity, basicity, and pKa9. Using organometallic reagents to make C-C bonds10. Conjugate addition11. Proton nuclear magnetic resonance12. Nucleophilic substitution at the carbonyl (C=O) group13. Equilibria, rates, and mechanisms: summary of mechanistic principles14. Nucleophilic substitution at C=O with loss of carbonyl oxygen15. Review of spectroscopic methods16. Stereochemistry17. Nucleophilic substitution at saturated carbon18. Conformational analysis19. Elimination reactions20. Electrophilic addition to alkenes21. Formation and reactions of enols and enolates22. Electrophilic aromatic substitution23. Electrophilic alkenes24. Chemoselectivity: selective reactions and protection25. Synthesis in action26. Alkylation of enolates27. Reactions of enolates with aldehydes and ketones: the aldol reaction28. Acylation at carbon29. Conjugate addition of enolates30. Retrosynthetic analysis31. Controlling the geometry of double bonds32. Determination of stereochemistry by spectroscopic33. Stereoselective reactions of cyclic compounds34. Diastereoselectivity35. Pericyclic reactions 1: cycloadditions36. Pericyclic reactions 2: sigmatropic and electrocyclic reactions37. Rearrangements38. Fragmentation39. Radical reactions40. Synthesis and reactions of carbenes41. Determining reaction mechanisms42. Saturated heterocycles and stereoelectronics43. Aromatic heterocycles 1: structures and reactions44. Aromatic heterocycles 2: synthesis45. Asymmetric synthesis46. Organo-main-group chemistry I: sulfur47. Organo-main-group chemistry II: boron, silicon, and tin48. Organometallic chemistry49. The chemistry of life50. Mechanisms in biological chemistry51. Natural products52. Polymerization53. Organic chemistry todayIndex
Synopsis
A new style of textbook, needed because almost all current organic chemistry texts are written to a fixed American pattern. This text is different from these in a number of important ways: The approach is based on explanation rather than fact. The functional group approach (alkane, alkene, alkyne) has served American State College readers well but increasingly students and instructors are attracted more to an approach based on mechanism and reaction type. This approach aims at understanding rather than factual knowledge and, though slower at the start, eventually gives the student power to understand compounds and reactions never previously encountered. This is a big advantage in a science already too large for individuals to learn and which is annually expanding at an ever greater rate. The basics of the subject are explained carefully and thoroughly. How to draw molecules realistically and how to draw mechanisms to reveal the fundamental chemistry are both emphasised. Important points are revisited when they become relevant in later chapters. Examples are very important too. New examples are given each time a concept resurfaces, and examples from everyday life and medicinal chemistry are frequently used. The authors want the readers to be excited by the universality of organic chemistry rather than be overwhelmed by facts. The design of the book has features to help comprehension. Structures are drawn in red, and black is used on them for emphasis. Other colours are used flexibly to draw attention to atoms, molecules, orbitals, arrows or whatever the authors want to emphasise rather than being used in a rigid systematic way. There are four types of "box" used to separate material from the main text, ranging from extra important summaries to diversions which can be omitted at first reading. The early chemistry chapters feature carbonyl group reactions because addition to carbonyl groups is probably the easiest reaction to understand. Thereafter the chemistry develops in a logical sequence but chapters on spectroscopy, stereochemistry etc are interspersed among those dealing with chemical reactions. From time to time review chapters summarise what has been described in a particular area. A personal and honest approach is adopted. The authors write clearly and directly to the reader, sharing their enthusiasms, understandings and doubts. If they believe an explanation is imperfect or controversial, they say so. They show that organic chemistry is developing rapidly, and that new ideas continually emerge to replace the old. The authors know from experience what conceptual difficulties often overwhelm students at an early stage in their studies and they devote more space to these points, give more examples, and revisit them when they can be applied. The aim is to help the readers master these points for themselves rather than just learn them off by heart., A first and second year undergraduate organic chemistry textbook, specifically geared to British and European courses and courses offerred in better schools in North America. The emphasis is on clarity and understanding, with very careful explanations of difficult concepts, many examples related to everyday life, and a fresh and student-friendly writing style., 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", 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: BL Building on: Details material from previous chapters that relate to the current chapter BL Arriving at: Provides a guide to the content of the chapter BL Looking forward to: Previews later chapters, which develop and expand the current material
LC Classification Number
QD251.3.O64 2001

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