Organic Chemistry By Jonathan Clayden, Nick Greeves & Stuart Warren 2nd Edition (informative)
Free download Organic Chemistry By Jonathan Clayden, Nick Greeves & Stuart Warren 2nd Edition
2nd Edition
Authors of: Organic Chemistry By Jonathan Clayden, Nick Greeves & Stuart Warren 2nd Edition
Jonathan Clayden
Nick Greeves
Stuart Warren
Table of Contents in Organic Chemistry By Jonathan Clayden, Nick Greeves & Stuart Warren 2nd Edition
Abbreviations xv
Preface to the second edition
Organic chemistry and this book
1 What is organic chemistry?
2 Organic structures
3 Determining organic structures
4 Structure of molecules
5 Organic reactions
6 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 group
11 Nucleophilic substitution 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 382
18 Review of spectroscopic methods
19 Electrophilic addition to alkenes
20 Formation and reactions of enols and enolates
21 Electrophilic aromatic substitution
22 Conjugate addition and nucleophilic aromatic 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 Aromatic heterocycles 1: reactions
30 Aromatic heterocycles 2: synthesis
31 Saturated heterocycles and stereoelectronics
32 Stereoselectivity in cyclic molecules
33 Diastereoselectivity
34 Pericyclic reactions 1: cycloadditions
35 Pericyclic reactions 2: 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
Figure acknowledgements
Periodic table of the elements
Index
The following is a comprehensive overview of the contents presented in the second edition of this book on organic chemistry, accompanied by brief summaries of each chapter:
**Abbreviations (xv):**
The list of abbreviations used throughout the book.
**Preface to the Second Edition:**
An introductory note providing insights into the reasons and improvements behind the creation of the second edition.
**Organic Chemistry and This Book:**
An exploration of the connection between organic chemistry and the content covered in the book, setting the stage for the subsequent chapters.
**1. What is Organic Chemistry?:**
An examination of the fundamental principles and characteristics that define organic chemistry.
**2. Organic Structures:**
A discussion on the various structures that form the basis of organic compounds.
**3. Determining Organic Structures:**
Insights into the methods and techniques employed in determining the structures of organic compounds.
**4. Structure of Molecules:**
An exploration of the molecular structures that play a crucial role in organic chemistry.
**5. Organic Reactions:**
A comprehensive overview of the different reactions that take place in organic chemistry.
**6. Nucleophilic Addition to the Carbonyl Group:**
Detailed insights into nucleophilic addition to carbonyl groups, a critical aspect of organic reactions.
**7. Delocalization and Conjugation:**
An examination of delocalization and conjugation phenomena within organic compounds.
**8. Acidity, Basicity, and pKa:**
A study of acidity, basicity, and pKa values in the context of organic chemistry.
**9. Using Organometallic Reagents to Make C–C Bonds:**
An exploration of the use of organometallic reagents in the synthesis of carbon-carbon bonds.
**10. Nucleophilic Substitution at the Carbonyl Group:**
In-depth coverage of nucleophilic substitution at carbonyl groups, a crucial reaction type.
**11. Nucleophilic Substitution at C=O with Loss of Carbonyl Oxygen:**
An examination of nucleophilic substitution reactions involving the loss of carbonyl oxygen.
**12. Equilibria, Rates, and Mechanisms:**
A discussion on equilibria, reaction rates, and the mechanisms that govern organic reactions.
**13. 1H NMR: Proton Nuclear Magnetic Resonance:**
A detailed exploration of proton nuclear magnetic resonance, an analytical technique used in organic chemistry.
**14. Stereochemistry:**
A comprehensive overview of stereochemistry, focusing on the three-dimensional arrangement of atoms.
**15. Nucleophilic Substitution at Saturated Carbon:**
A detailed examination of nucleophilic substitution reactions involving saturated carbon atoms.
**16. Conformational Analysis:**
An exploration of conformational analysis, studying the different spatial arrangements of atoms in a molecule.
**17. Elimination Reactions:**
A comprehensive coverage of elimination reactions in organic chemistry.
**18. Review of Spectroscopic Methods:**
A revisit of various spectroscopic methods used in the analysis of organic compounds.
**19. Electrophilic Addition to Alkenes:**
An in-depth exploration of electrophilic addition reactions involving alkenes.
**20. Formation and Reactions of Enols and Enolates:**
Insights into the formation and reactions of enols and enolates, crucial intermediates in organic chemistry.
**21. Electrophilic Aromatic Substitution:**
A detailed examination of electrophilic aromatic substitution reactions.
**22. Conjugate Addition and Nucleophilic Aromatic Substitution:**
An exploration of conjugate addition and nucleophilic aromatic substitution reactions.
**23. Chemoselectivity and Protecting Groups:**
An examination of chemoselectivity and the use of protecting groups in organic synthesis.
**24. Regioselectivity:**
A study of regioselectivity in organic reactions, focusing on the preferential formation of specific regioisomers.
**25. Alkylation of Enolates:**
Insights into the alkylation reactions involving enolates.
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