book organic chemistry by oxford in pdf
Jonathan Clayden
Nick Greeves
Stuart Warren
Peter Wothers
this is the book of organic chemistry in pdf written by Jonathan Clayden and Nick Greeve and Stuart Warren and Peter Wothers published by oxford universitie in 2001 of professors of science faculties universities.
Information about the book
Language of the book: English language
Book Title: organic chemistry Clayden,Greeves
Scriptwriter: by Jonathan Clayden and Nick Greeves Warren and Wothers and Stuart Warren and Peter Wothers
Year of printing: published by oxford universitie in 2001
File Format:PDF
Number of chapters: 53 chapters
Number of pages: 1516 pages
File Size: 34 MB
this is the book of organic chemistry in pdf written by Jonathan Clayden and Nick Greeve and Stuart Warren and Peter Wothers published by oxford universitie in 2001 of professors of science faculties universities.
Information about the book
Language of the book: English language
Book Title: organic chemistry Clayden,Greeves
Scriptwriter: by Jonathan Clayden and Nick Greeves Warren and Wothers and Stuart Warren and Peter Wothers
Year of printing: published by oxford universitie in 2001
File Format:PDF
Number of chapters: 53 chapters
Number of pages: 1516 pages
File Size: 34 MB
Book Title: organic chemistry Clayden,Greeves
Scriptwriter: by Jonathan Clayden and Nick Greeves Warren and Wothers and Stuart Warren and Peter Wothers
Year of printing: published by oxford universitie in 2001
File Format:PDF
Number of chapters: 53 chapters
Number of pages: 1516 pages
File Size: 34 MB
Contents
- What is organic chemistry? Organic chemistry and this book
- Organic structures
- Determining organic structures
- Structure of molecules
- Organic reactions
- Nucleophilic addition to the carbonyl group
- Delocalization and conjugation
- Acidity, basicity, and pKa
- Using organometallic reagents to make C-C bonds
- Conjugate addition
- Proton nuclear magnetic resonance
- Nucleophilic substitution at the carbonyl (C=0) group
- Equilibria, rates, and mechanisms: summary of mechanistic principles
Nucleophilic
- substitution at C=0 with loss of carbonyl oxygen
- Review of spectroscopic methods
- Stereochemistry
- Nucleophilic substitution at saturated carbon
- Conformational analysis
- Elimination reactions
- Electrophilic addition to alkenes
- Formation and reactions of enols and enolates
- Electrophilic aromatic substitution
- Electrophilic alkenes
- Chemoselectivity: selective reactions and protection
- Synthesis in action
- Alkylation of enolates
- Reactions of enolates with aldehydes and ketones: the aldol reaction
- Acylation at carbon
- Conjugate addition of enolates
- Retrosynthetic analysis
- Controlling the geometry of double bonds
- Determination of stereochemistry by spectroscopic methods
- Stereoselective reactions of cyclic compounds
- Diastereoselectivity
- Pericyclic reactions 1: cycloadditions
- Pericyclic reactions 2: sigmatropic and electrocyclic reactions
- Rearrangements
- Fragmentation
- Radical reactions
- Synthesis and reactions of carbenes
- Determining reaction mechanisms
- Saturated heterocycles and stereoelectronics
- Aromatic heterocycles 1: structures and reactions
- Aromatic heterocycles 2: synthesis
- Asymmetric synthesis
- Organo-main-group chemistry I: sulfur
- Organo-main-group chemistry II: boron, silicon, and tin
- Organometallic chemistry
- The chemistry of life
- Mechanisms in biological chemistry
- Natural products
- Polymerization
- Organic chemistry today and Index
DOWNLOAD THE BOOK
Free download Book organic chemistry by oxford in pdf
Contents
- What is organic chemistry? Organic chemistry and this book
- Organic structures
- Determining organic structures
- Structure of molecules
- Organic reactions
- Nucleophilic addition to the carbonyl group
- Delocalization and conjugation
- Acidity, basicity, and pKa
- Using organometallic reagents to make C-C bonds
- Conjugate addition
- Proton nuclear magnetic resonance
- Nucleophilic substitution at the carbonyl (C=0) group
- Equilibria, rates, and mechanisms: summary of mechanistic principles Nucleophilic
- substitution at C=0 with loss of carbonyl oxygen
- Review of spectroscopic methods
- Stereochemistry
- Nucleophilic substitution at saturated carbon
- Conformational analysis
- Elimination reactions
- Electrophilic addition to alkenes
- Formation and reactions of enols and enolates
- Electrophilic aromatic substitution
- Electrophilic alkenes
- Chemoselectivity: selective reactions and protection
- Synthesis in action
- Alkylation of enolates
- Reactions of enolates with aldehydes and ketones: the aldol reaction
- Acylation at carbon
- Conjugate addition of enolates
- Retrosynthetic analysis
- Controlling the geometry of double bonds
- Determination of stereochemistry by spectroscopic methods
- Stereoselective reactions of cyclic compounds
- Diastereoselectivity
- Pericyclic reactions 1: cycloadditions
- Pericyclic reactions 2: sigmatropic and electrocyclic reactions
- Rearrangements
- Fragmentation
- Radical reactions
- Synthesis and reactions of carbenes
- Determining reaction mechanisms
- Saturated heterocycles and stereoelectronics
- Aromatic heterocycles 1: structures and reactions
- Aromatic heterocycles 2: synthesis
- Asymmetric synthesis
- Organo-main-group chemistry I: sulfur
- Organo-main-group chemistry II: boron, silicon, and tin
- Organometallic chemistry
- The chemistry of life
- Mechanisms in biological chemistry
- Natural products
- Polymerization
- Organic chemistry today and Index
DOWNLOAD THE BOOK
Free download Book organic chemistry by oxford in pdf
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