gogogo
Syndetics cover image
Image from Syndetics

Organic chemistry / Jonathan Clayden ... [et al.].

By: Material type: TextTextPublication details: Oxford ; New York : Oxford University Press, 2001.Description: 1512 p. : col. ill. ; 28 cmISBN:
  • 0198503466
  • 9780198503460
Other title:
  • Clayden, Greenves, Warren and Wothers Organic chemistry [Cover title]
Subject(s): DDC classification:
  • 547 CLA
Holdings
Item type Current library Call number Copy number Status Date due Barcode
Standard Loan Moylish Library Main Collection 547 CLA (Browse shelf(Opens below)) 1 Available 39002100331520

Enhanced descriptions from Syndetics:

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.

Includes bibliographical references and index.

Table of contents provided by Syndetics

  • List (Page 1)
  • 1 What is Organic Chemistry?
  • 2 Organic Structures
  • 3 Determining Organic Structures
  • 4 Structure of Molecules
  • 5 Organic Reactions
  • 6 Nucleophilic Addition to the C=O Group
  • 7 Conjugation/Delocalisation and UV spectra
  • 8 Acidity and Basicity of Organic Molecules
  • 9 Formation of C-C fromC=O Bonds by Organo-Metallic reagents
  • 10 Conjugate Addition and Substitution
  • 11 Proton NMR Spectroscopy
  • 12 Nucleophilic Substitution at the C=O Group
  • 13 Review Chapter: Summary of Mechanistic Principles
  • 14 Addition to C=O with Loss of Carbonyl Oxygen
  • 15 Review Chapter on SpectroscopicMethods
  • 16 Stereochemistry
  • 17 Nucleophilic Substitution at Saturated Carbon
  • 18 Conformational Analysis
  • 19 Elimination Reactions
  • 20 Electrophilic Addition to Alkenes
  • 21 Formation and Reactions of Enolates
  • 22 Electrophilic Aromatic Substitution
  • 23 Electrophilic Alkenes: ConjugateAddition, Allylic Systems and Nucleophilic Aromatic Substitution
  • 24 Chemoselectivity, Protection, Oxidation and Reductio

Author notes provided by Syndetics

Jonathan Clayden is at University of Manchester. Nick Greeves is at University of Liverpool.

Powered by Koha