Clayden, Greeves, & Warren: Organic Chemistry 2e Free Pdf Download
- Description
- About the Author(s)
- Table of Contents
- Reviews
- Boosted Resource
Description
Inspiring and motivating students from the moment information technology published, Organic Chemistry has established itself in simply one edition every bit the students' choice of organic chemistry text. Its explanatory, mechanistic, evidence-based arroyo makes it perfect for fostering a true understanding of the subject.
- The class companion of pick for a generation of chemistry students.
- Accent is on understanding rather than learning facts: organic chemistry emerges as a coherent whole, with numerous logical connections and consequences, and with an underlying structure and language.
- Accent on mechanism, orbitals, and stereochemistry means that the student emerges with solid agreement of important factors common to all reactions, allowing interpretation/prediction of reactions not previously met.
- Direct, personal, student-friendly writing style draws in and engages the reader, motivating them to learn more.
- Extensive online support takes learning beyond the printed book, enhancing understanding notwithstanding further.
- Besides available as an e-book with functionality, navigation features, and links that offering extra learning support
New to this edition
- All chapters have been reviewed and refined to provide a more student-friendly, more logical, and more coherent presentation of the subject as a whole.
- Chapters are extensively cross-linked to a depository financial institution of over 500 interactive online resources, which assist readers to visualise molecular structure, and gain a deeper and richer understanding of reaction mechanisms.
- Early chapters accept been recast to requite a more carefully-graded learning bend, to avoid the student existence confronted by besides much, likewise soon.
- Coverage of topics with particular applied relevance that have adult in the terminal ten years has been enhanced, including the presentation of metathesis, mod methods of disproportionate synthesis (including organic catalysis), 'click chemistry', and palladium-catalysed couplings.
- A re-ordering of topics has brought new coherence to the coverage of subjects such as conjugate addition, which had previously been dispersed through the volume, and has brought certain key topics, such as heterocyclic chemistry, earlier.
- A new chapter on regioselectivity has been introduced.
- Coverage of certain topics, including enolate chemistry, has been refined to give more focus to the volume as a whole and tailor it more than closely to the needs of undergraduates.
- Suggestions for further reading have been added to most chapters to assist students take the adjacent pace in their learning.
About the Author(s)
Jonathan Clayden, Professor of Organic Chemistry, University of Manchester, Nick Greeves, Senior Lecturer, University of Liverpool, and Stuart Warren, Formerly Reader in Organic Chemistry, University of Cambridge and Swain of Churchill College, Cambridge
Jonathan Clayden is a Professor of Organic Chemical science at the Academy of Manchester, where he and his inquiry grouping work on the structure of molecules with defined shapes - in detail those where command of conformation and limitation of flexibility is important. Jonathan was awarded a BA (Natural Sciences) from Churchill College, Cambridge before completing his PhD with Stuart Warren, besides at the University of Cambridge. He has been at the Academy of Manchester since 1994.
Nick Greeves is the Director of Teaching and Learning in the Department of Chemistry at the Academy of Liverpool. Nick is a Cambridge graduate, obtaining his PhD there in 1986 for piece of work on the stereoselective Horner-Wittig reaction with Stuart Warren. He and so held a Harkness Fellowship at the Academy of Wisconsin-Madison and at Stanford University, California, and a Enquiry Fellowship at Cambridge University before joining Liverpool in 1989 where he is currently a Senior Lecturer.
Stuart Warren is a quondam lecturer in the Department of Chemical science at the University of Cambridge and Swain of Churchill College, Cambridge. A graduate of Trinity Higher, Cambridge, Stuart completed his PhD at Cambridge with Malcolm Clark before conveying out postal service-doctoral enquiry at Harvard Academy. He became a educational activity boyfriend at Churchill Higher in 1971, and remained a lecturer and researcher at Cambridge until his retirement in 2006.
Table of Contents
- 1:What is organic chemistry?
2:Organic structures
3:Determining organic structures
4:Construction of molecules
5:Organic reactions
half-dozen:Nucleophilic addition to the carbonyl group
7:Delocalization and conjugation
8:Acidity, basicity, and pKa
9:Using organometallic reagents to make C-C bonds
10:Nucleophilic substitution at the carbonyl grouping
xi:Nucleophilic commutation at C=O with loss of carbonyl oxygen
12:Equilibria, rates and mechanisms
13:1H NMR: Proton nuclear magnetic resonance
14:Stereochemistry
15:Nucleophilic substitution at saturated carbon
16:Conformational analysis
17:Elimination reactions
eighteen:Review of spectroscopic methods
19:Electrophilic addition to alkenes
20:Formation and reactions of enols and enolates
21:Electrophilic effluvious exchange
22:Cohabit add-on and nucleophilic effluvious substitution
23:Chemoselectivity and protecting groups
24:Regioselectivity
25:Alkylation of enolates
26:Reactions of enolates with carbonyl compounds: the aldol and Claisen reactions
27:Sulfur, silicon and phosphorus in organic chemistry
28:Retrosynthetic analysis
29:Effluvious heterocycles 1: structures and reactions
thirty:Aromatic heterocycles ii: synthesis
31:Saturated heterocycles and stereoelectronics
32:Stereoselectivity in circadian molecules
33:Diastereoselectivity
34:Pericyclic reactions one: cycloadditions
35:Pericyclic reactions two: sigmatropic and electrocyclic reactions
36:Participation, rearrangement and fragmentation
37:Radical reactions
38:Synthesis and reactions of carbenes
39:Determining reaction mechanisms
40:Organometallic chemistry
41:Asymmetric synthesis
42:Organic chemistry of life
43:Organic chemistry today
Reviews
"Information technology is a credit to the authors that a textbook that I have adored for then many years has undergone such a substantial overhaul and yet still retains the features that fabricated it quite and so attractive to students in the first place. This is a book that volition continue to inspire students of organic chemical science for many years to come. Even if you already have the first edition, I am happy to recommend that you invest in this new version y'all will non be disappointed." - John Hayward, in Chemical science World, December 2012
"Review from previous edition This is a book nosotros have all been waiting for! It is based on sound mechanistic reasoning and contains thousands of useful examples for teaching. Its manner is approachable and covers both primal and more advanced material." - Adam Nelson, Lecturer, University of Leeds
"Review from previous edition Represents a milestone in the field of organic chemistry textbooks... This is the first organic textbook that could be used in some shape or form on almost every organic chemistry course in any U.k. undergraduate programme... I soon expect to be hearing "You tin can expect information technology up in Clayden" ringing from lectures and tutorials, and for many years to come." - Andrew Boa in The Times Higher Education, 2001
Additional Resources
Online Resource Centre
For students:
Interactive 3D animations via chemtube3d
Additional capacity
A range of problems to back-trail each chapter
For registered adopters of the text:
Figures from the book in electronic format
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