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Organic reaction mechanisms /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Bansal, Raj K. (Autor)
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Kent [England] : New Academic Science Limited, 2013.
Edición:Fourth edition.
Temas:
Acceso en línea:Texto completo

MARC

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100 1 |a Bansal, Raj K.,  |e author. 
245 1 0 |a Organic reaction mechanisms /  |c Raj K. Bansal. 
250 |a Fourth edition. 
264 1 |a Kent [England] :  |b New Academic Science Limited,  |c 2013. 
264 4 |c ©2013 
300 |a 1 online resource (565 pages) :  |b illustrations 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
504 |a Includes bibliographical references at the end of each chapters and index. 
588 0 |a Online resource; title from PDF title page (ebrary, viewed September 8, 2015). 
505 8 |6 880-01  |a 2.5 Consecutive Reactions 2.6 Parallel or Concurrent Reactions ; 2.7 Reaction Rate Theory ; 2.8 Temperature Dependence of Rate Constant ; 2.9 Reaction Intermediates ; 2.10 Principle of Microscopic Reversibility ; 2.13 Chemical Evidence For Reaction Mechanisms ; 2.14 Kinetic Isotope Effects ; References ; Review Problems ; Chapter 3 Concept of Acids and Bases ; 3.1 Brönsted-Lowry Concept ; 3.2 Ionization of Acids and Bases ; 3.3 Lewis Concept of Acids and Bases ; 3.4 Acidity Function ; 3.5 Catalysis ; 3.6 Acid-Base Catalysis ; 3.7 Brönsted Relation. 
505 8 |a 3.8 Hard and Soft Acids and Bases References ; Review Problems ; Chapter 4 Nucleophilic Displacement Reactions ; 4.1 Substitution Nucleophilic Bimolecular (SN2) ; 4.2 Substitution Nucleophilic Unimolecular (SN1) ; 4.3 Substitution at Bridgehead Halides ; 4.4 Isotope Effects In Substitution Reactions ; 4.5 Solvent Effects In Substitution Reactions ; 4.6 Salt Effects in Substitution Reactions ; 4.7 Ion-Pair Mechanism for SN1 Reactions ; 4.8 Substitution Nucleophilic Internal (SNi) ; 4.9 Substitution at Allylic and Allylenic Carbon Atom. 
505 8 |a 4.10 Special Cases in Substitution Reactions 4.11 Reactivity in Cyclic Strained Compounds ; 4.12 The Bridgehead Carbocation Controversy ; References ; Review Problems ; Chapter 5 Organic Preparative Reactions ; 5.1 The Baeyer-Villiger Oxidation ; 5.2 The Meerwein-Ponndorf-Verley Reduction ; 5.3 The Clemmensen Reduction ; 5.4 The Wolff-Kishner Reduction ; 5.5 The Birch Reduction ; 5.6 The Aldol Condensation ; 5.7 The Benzoin Condensation ; 5.8 The Claisen Ester Condensation ; 5.9 The Darzens Condensation ; 5.10 The Perkin Condensation ; 5.11 The Hunsdiecker Reaction. 
505 8 |a 5.12 Grignard Reagents 5.13 Carbenes ; 5.14 The Wittig Reaction ; 5.15 Enamines ; 5.16 The Mannich Reaction ; 5.17 The Diels-Alder Reaction ; References ; Review Problems ; Chapter 6 Free Radical Reactions ; 6.1 Geometry of Free Radicals ; 6.2 Stability of Free Radicals ; 6.3 The Detection of Free Radicals ; 6.4 Production of Free Radicals ; 6.5 Properties of Free Radicals ; 6.6 Types of Free Radical Reactions ; 6.7 Radical Halogenation of Hydrocarbons ; 6.8 Autoxidation ; 6.9 Free Radical Rearrangements ; 6.10 Radical Cyclization and Ring Expansion. 
546 |a Text in English. 
590 |a ProQuest Ebook Central  |b Ebook Central Academic Complete 
650 0 |a Chemistry, Organic. 
650 0 |a Organic reaction mechanisms. 
650 6 |a Chimie organique. 
650 6 |a Réactions organiques (Chimie)  |x Mécanismes. 
650 7 |a organic chemistry.  |2 aat 
650 7 |a Chemistry, Organic  |2 fast 
650 7 |a Organic reaction mechanisms  |2 fast 
758 |i has work:  |a Organic Reaction Mechanisms (Text)  |1 https://id.oclc.org/worldcat/entity/E39PCG3fGwTFQjb6VXY87x6K7d  |4 https://id.oclc.org/worldcat/ontology/hasWork 
776 0 8 |i Print version:  |a Bansal, Raj K.  |t Organic reaction mechanisms.  |b Fourth edition.  |d Kent, [England] : New Academic Science Limited, ©2013  |h xv, 548 pages  |z 9781906574666 
856 4 0 |u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=3440199  |z Texto completo 
880 0 |6 505-01/(S  |a Cover ; Preface ; Contents ; Chapter 1 Basic Concepts ; 1.1 Bond Dissociation Energy ; 1.2 Electronegativity ; 1.3 Dipole Moment ; 1.4 Hydrogen Bond ; 1.5 Hyperconjugation (Interaction Between σ- and π-Systems) ; 1.6 Inductive and Field Effects ; 1.7 Steric Effects ; 1.8 Bredt's Rule ; 1.9 Aromaticity ; 1.10 The Hammett Equation ; References ; Review Problems ; Chapter 2 Chemical kinetics and the Study of reaction Mechanisms ; 2.1 Bond Cleavage and Reaction Intermediates ; 2.2 Chemical Kinetics ; 2.3 Rate of Reaction ; 2.4 Order of Reaction. 
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