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|Additional Physical Format:||Print version:
Sun, Xiaoping, 1960-
Hoboken, New Jersey : Wiley, 
|Material Type:||Document, Internet resource|
|Document Type:||Internet Resource, Computer File|
|All Authors / Contributors:||
|ISBN:||9781118507971 1118507975 9781118507919 1118507916|
|Notes:||Machine generated contents note: Chapter 1 Fundamental Principles 1.1 Reaction mechanisms and their importance 1.2 Elementary (concerted) and stepwise reactions 1.3 Molecularity 1.4 Kinetics 1.5 Thermodynamics 1.6 The transition state 1.7 The molecular orbital theory 1.8 Electrophiles/nucleophiles versus acids/bases 1.9 Isotope labeling References Problems Chapter 2 The Aliphatic C-H Bond Functionalization 2.1 Alkyl radicals: Bonding and their relative stability 2.2 Radical halogenations of the C-H bonds on sp3-hybridized carbons: Mechanism and nature of the transition states 2.3 Energetics of the radical halogenations of alkanes and their regioselectivity 2.4 Kinetics of radical halogenations of alkanes 2.5 Radical initiators 2.6 Transition-metal-compounds catalyzed alkane C-H bond activation and functionalization 2.7 Superacids catalyzed alkane C-H bond activation and functionalization 2.8 Nitration of aliphatic C-H bonds via the nitronium NO2+ ion 2.9 Enzyme catalyzed alkane C-H bond activation and functionalization: Biochemical methods References Problems Chapter 3 Functionalization of the Alkene C=C Bond by Electrophilic Additions 3.1 Markovnikov additions via intermediate carbocations 3.2 Electrophilic addition of hydrogen halides to conjugated dienes 3.3 Non-Markovnikov radical addition 3.4 Hydroboration: Concerted, Non-Markovnikov syn-addition 3.5 Transition-metal catalyzed hydrogenation of the alkene C=C bond (syn-addition) 3.6 Halogenation of the alkene C=C bond (Anti-addition): Mechanism and its stereochemistry References Problems Chapter 4 Functionalization of the Alkene C=C Bond by Cycloaddition Reactions 4.1 Cycloadditions of the alkene C=C bond to form three-membered rings 4.2 Cycloadditions to form four-membered rings 4.3 Deals-Alder cycloadditions of the alkene C=C bond to form six-membered rings 4.4 1,3-Dipolar cycloadditions of the C=C and other multiple bonds to form five-membered rings 4.5 Pericyclic reactions References Problems Chapter 5 The Aromatic C-H bond Functionalization and Related Reactions 5.1 Aromatic nitration: All reaction intermediates and full mechanism for the aromatic C-H bond substitution by nitronium (NO2+) and related electrophiles 5.2 Mechanisms and synthetic utility for aromatic C-H bond substitutions by other related electrophiles 5.3 The electrophilic aromatic C-H bond substitution reactions via SN1 and SN2 mechanisms 5.4 Substituent effects on the electrophilic aromatic substitution reactions 5.5 Isomerizations effected by the electrophilic aromatic substitution reactions 5.6 Electrophilic substitution reactions on the aromatic carbon-metal bonds: Mechanisms and synthetic applications 5.7 Nucleophilic aromatic substitution via a benzyne (aryne) intermediate: Functional group transformations on aromatic rings 5.8 Nucleophilic aromatic substitution via an anionic Meisenheimer complex 5.9 Biological applications of functionalized aromatic compounds References Problems Chapter 6 Nucleophilic Substitutions on sp3-Hybridized Carbons: Functional Group Transformations 6.1 Nucleophilic substitution on mono-functionalized sp3-hybridized carbon 6.2 Functional groups which are good and poor leaving groups 6.3 Good and poor nucleophiles 6.4 SN2 reactions: Kinetics, mechanism, and stereochemistry 6.5 Analysis of the SN2 mechanism using symmetry rules and molecular orbital theory 6.6 SN1 reactions: Kinetics, mechanism, and product development 6.7 Competitions between SN1 and SN2 reactions 6.8 Some useful SN1 and SN2 reactions: Mechanisms and synthetic perspectives 6.9 Biological applications of nucleophilic substitution reactions References Problems Chapter 7 Eliminations 7.1 E2 Elimination: Bimolecular b-elimination of H/LG and its regiochemistry and stereochemistry 7.2 Analysis of the E2 mechanism using symmetry rules and molecular orbital theory 7.3 Basicity versus nucleophilicity for various anions 7.4 Competition of E2 and SN2 reactions 7.5 E1 Elimination: Stepwise b-elimination of H/LG via an intermediate carbocation and its rate-law 7.6 Special b-elimination reactions 7.7 Elimination of LG1/LG2 in the compounds that contain two functional groups 7.8 a-Elimination giving a carbene: A mechanistic analysis using symmetry rules and molecular orbital theory 7.9 E1cb elimination and its biological applications References Problems Chapter 8 Nucleophilic Additions and Substitutions on Carbonyl Groups 8.1 Nucleophilic additions and substitutions of carbonyl compounds 8.2 Nucleophilic additions of aldehydes and ketones and their biological applications 8.3 Biological hydride donors NAD(P)H and FADH2 8.4 Activation of carboxylic acids via nucleophilic substitutions on the carbonyl carbons 8.5 Nucleophilic substitutions of acyl derivatives and their biological applications 8.6 Reduction of acyl derivatives by hydride donors 8.7 Kinetics of the Nucleophilic addition and substitution of acyl derivatives References Problems Chapter 9 Reactivity of the a-Hydrogen to Carbonyl Groups 9.1 Formation of enolates and their nucleophilicity 9.2 Alkylation of carbonyl compounds (aldehydes, ketones, and esters) via enolates and hydrazones 9.3 Aldol reactions 9.4 Acylation reactions of esters via enolates: Mechanism and synthetic utility 9.5 Roles of enolates in metabolic processes in living organisms References Problems Chapter 10 Rearrangements 10.1 Major types of rearrangements 10.2 Rearrangement of carbocations: 1,2-Shift 10.3 Neighboring leaving group facilitated 1,2-rearrangement 10.4 Carbene rearrangement: 1,2-Rearrangement of hydrogen facilitated by a lone pair of electrons 10.5 Claisen rearrangement 10.6 Photochemical isomerization of alkenes and its biological applications 10.7 Rearrangement of carbon-nitrogen-sulfur containing heterocycles References Problems.|
|Description:||1 online resource.|
|Contents:||ORGANIC MECHANISMS; Contents; Preface; 1 Fundamental Principles; 1.1 Reaction Mechanisms and their Importance; 1.2 Elementary (Concerted) and Stepwise Reactions; 1.3 Molecularity; 1.3.1 Unimolecular Reactions; 1.3.2 Bimolecular Reactions; 1.4 Kinetics; 1.4.1 Rate Laws for Elementary (Concerted) Reactions; 1.4.2 Reactive Intermediates and the Steady-State Assumption; 1.4.3 Rate Laws for Stepwise Reactions; 1.5 Thermodynamics; 1.5.1 Enthalpy, Entropy, and Free Energy; 1.5.2 Reversible and Irreversible Reactions; 1.5.3 Chemical Equilibrium; 1.6 The Transition State 1.7 The Molecular Orbital Theory1.7.1 Formation of Molecular Orbitals from Atomic Orbitals; 1.7.2 Molecular Orbital Diagrams; 1.7.3 Resonance Stabilization; 1.7.4 Frontier Molecular Orbitals; 1.8 Electrophiles/Nucleophiles versus Acids/Bases; 1.8.1 Common Electrophiles; 1.8.2 Common Nucleophiles; 1.9 Isotope Labeling; Problems; References; 2 The Aliphatic C H Bond Functionalization; 2.1 Alkyl Radicals: Bonding and their Relative Stability; 2.2 Radical Halogenations of the C H Bonds on sp3-Hybridized Carbons: Mechanism and Nature of the Transition States 2.3 Energetics of the Radical Halogenations of Alkanes and their Regioselectivity2.3.1 Energy Profiles for Radical Halogenation Reactions of Alkanes; 2.3.2 Regioselectivity for Radical Halogenation Reactions; 2.4 Kinetics of Radical Halogenations of Alkanes; 2.5 Radical Initiators; 2.6 Transition-Metal-Compounds-Catalyzed Alkane C H Bond Activation and Functionalization; 2.6.1 The C H Bond Activation via Agostic Bond; 2.6.2 Mechanisms for the C H Bond Oxidative Functionalization; 2.7 Superacids-Catalyzed Alkane C H Bond Activation and Functionalization 2.8 Nitration of Aliphatic C H Bonds via the Nitronium NO2+ Ion2.9 Enzyme-Catalyzed Alkane C H Bond Activation and Functionalization: Biochemical Methods; Problems; References; 3 Functionalization of the Alkene C C Bond by Electrophilic Additions; 3.1 Markovnikov Additions via Intermediate Carbocations; 3.1.1 Additions of Alkenes to Hydrogen Halides (HCl, HBr, and HI): Mechanism, Regiochemistry, and Stereochemistry; 3.1.2 Acid- and Transition-Metal-Catalyzed Hydration of Alkenes and Its Applications; 3.1.3 Acid-Catalyzed Additions of Alcohols to Alkenes 3.1.4 Special Electrophilic Additions of the Alkene C C Bond: Mechanistic and Synthetic Aspects3.1.5 Electrophilic Addition to the C C Triple Bond via a Vinyl Cation Intermediate; 3.2 Electrophilic Addition of Hydrogen Halides to Conjugated Dienes; 3.3 Non-Markovnikov Radical Addition; 3.4 Hydroboration: Concerted, Non-Markovnikov syn-Addition; 3.4.1 Diborane (B2H6): Structure and Properties; 3.4.2 Concerted, Non-Markovnikov syn-Addition of Borane (BH3) to the Alkene C C Bond: Mechanism, Regiochemistry, and Stereochemistry; 3.4.3 Synthesis of Special Hydroborating Reagents|
|Responsibility:||Xiaoping Sun, University of Charleston, Charleston, West Virginia, USA.|
Emphasizing mechanistic aspects of organic reactions, Organic Mechanisms provides a useful guide for how to analyze, understand, approach, and solve the problems of organic reactions with the help of mechanistic studies.
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