Theory of Organic Reactions - Couverture souple

Epiotis, N. D. D.

9783642668296: Theory of Organic Reactions

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ISBN 10 : 3642668291 ISBN 13 : 9783642668296

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�diteur: Springer
Date d'�dition: 2011
Langue: anglais
ISBN 10: 3642668291
ISBN 13: 9783642668296
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Nombre de pages: 312
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Theory of Organic Reactions (eng)

Epiotis, N. D.

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ISBN 10 : 3642668291 ISBN 13 : 9783642668296

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Theory of Organic Reactions

N. D. Epiotis

Edit� par Springer Berlin Heidelberg Okt 2011, 2011

ISBN 10 : 3642668291 ISBN 13 : 9783642668296

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Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Inhaltsangabe1. One-Determinental Theory of Chemical Reactivity.- 1.1 General Principles and Computational Schemes.- 1.2 Qualitative One-Determinental Models of Chemical Reactivity.- 1.3 The Static One Electron Molecular Orbital Model.- 1.4 Orbital Energies. The Donor-Acceptor Classification of Molecules and the Concept of Reaction Polarity.- 1.5 One Electron Interaction Matrix Elements and Overlap Integrals.- 1.6 The Woodward-Hoffmann Molecular Orbital Correlation Diagram.- 2. Configuration Interaction Overview of Chemical Reactivity.- 2.1 General Principles.- 2.2 Qualitative Configuration Interaction Models of Chemical Reactivity.- 2.3 The Static Linear Combination of Fragment Configurations Method.- 2.4 The Static Delocalized Configuration Interaction Method.- 2.5 The Dynamic Delocalized Configuration Interaction Method.- 3. The Dynamic Linear Combination of Fragment Configurations Method.- 3.1 Definitions.- 3.2 General Theoretical Considerations.- 3.3 The Interaction of Diabatic Surfaces.- 3.4 Polarity Control of Barrier Heights and Decay Efficiencies.- 3.5 The Effect of Excitation Energy on Photochemical Barrier Height.- 3.6 Diabatic Surface Interrelationships. A Classification of Chemical Reactions.- 4. Even-Even Intermodular Multicentric Reactions.- 4.1 Potential Energy Surfaces for 2 +2 Cycloadditions.- 4.2 The Effect of Polarity. Potential Energy Surfaces for Nonionic and Ionic In 2 +2 Cycloadditions.- 4.3 Pericyclic, Effectively Pericyclic and Quasipericyclic Reactions.- 4.4 The Effect of Unsymmetrical Substitution and the Effect of Conjugative Substitution.- 4.5 The Regiochemistry of 2 +2 Cycloadditions.- 4.6 Isomeric Reactions and the Topochemistry of 2 +2 Cycloreversions.- 4.7 The Topochemistry of Intramolecular Cycloadditions.- 4.8 The Selectivity-Polarity Relationship.- 4.9 Reaction Intermediates and Types of Organic Mechanisms.- 4.10 2 +2 Nonionic Photocycloadditions Involving n \* Excitation.- 4.11 The Effect of Low Lying Diexcited Diabatic Surfaces in Photoreactions.- 4.12 The Problem of Energy Wastage. The Concept of Dual Channel Photoreactions.- 4.13 Generalizations.- 5. The Problem of Correlation Imposed Barriers.- 6. Reactivity Trends of Thermal Cycloadditions.- 6.1 Introduction.- 6.2 Mechanisms of Stereochemical Nonretention in Cycloadditions.- 6.3 Reactivity Trends of Thermal Nonionic 2 +2 Cycloadditions.- 6.4 Reactivity Trends of Thermal Ionic 2 +2 Cycloadditions.- 6.5 The 2 +2 Ionic Cycloaddition Problem.- 6.6 Reactivity Trends of Thermal Nonionic 4 +2 Cycloadditions.- 6.7 Reactivity Trends of Thermal Ionic 4 +2 Cycloadditions.- 7. Reactivity Trends of Singlet Photochemical Cycloadditions.- 7.1 Introduction.- 7.2 The Chorochemistry of Singlet 2 +2 Photocycloadditions.- 7.3 'Unusual' Head to Head vs. Head to Tail Regioselectivity of Photocycloadditions.- 7.4 n \* State Dual Channel Mechanisms of Polar Nonionic Carbonyl Photocycloadditions.- 7.5 \* State Dual Channel Mechanisms of Polar Nonionic Photocycloadditions.- 8. Miscellaneous Intermolecular Multicentric Reactions.- 8.1 Cycloadditions of Cumulene Systems.- 8.2 The Ene Reaction.- 8.3 1,3 Dipolar Cycloadditions.- 9. A ddition Reactions.- 9.1 Introduction.- 9.2 Potential Energy Surfaces for 2 +2 Additions.- 9.3 Reactivity Trends of 2 +2 Additions.- 10. Even-Odd Multicentric Intermolecular Reactions.- 10.1 Potential Energy Surfaces for 2 +1 Cycloadditions.- 10.2 Reactivity Trends of Cationic Even-Odd Retro-Cycloadditions and Eliminations.- 11. Potential Energy Surfaces for Odd-Odd Multicentric Intermolecular Reactions.- 12. Even-Even Intermolecular Bicentric Reactions.- 12.1 Potential Energy Surfaces for Electrophilic and Nucleophilic Additions.- 12.2 Reactivity Trends of Electrophilic and Nucleophilic Substitutions.- 13. Even-Odd Intermolecular Bicentric Reactions.- 13.1 Potential Energy Surfaces for Radical Additions.- 13.2 Reactivity Trends of Radical Substitution Reactions.- 14. N� de r�f. du vendeur 9783642668296

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Theory of Organic Reactions

Epiotis, N. D. D.

Edit� par Springer, 2011

ISBN 10 : 3642668291 ISBN 13 : 9783642668296

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Theory of Organic Reactions

N. D. Epiotis

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ISBN 10 : 3642668291 ISBN 13 : 9783642668296

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Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. 1. One-Determinental Theory of Chemical Reactivity.- 1.1 General Principles and Computational Schemes.- 1.2 Qualitative One-Determinental Models of Chemical Reactivity.- 1.3 The Static One Electron Molecular Orbital Model.- 1.4 Orbital Energies. The Donor-A. N� de r�f. du vendeur 5067648

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Theory of Organic Reactions

N. D. Epiotis

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ISBN 10 : 3642668291 ISBN 13 : 9783642668296

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Theory of Organic Reactions

Epiotis N. D.

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ISBN 10 : 3642668291 ISBN 13 : 9783642668296

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Etat : New. Print on Demand pp. 312 69 Figures, 67:B&W 6.69 x 9.61 in or 244 x 170 mm (Pinched Crown) Perfect Bound on White w/Gloss Lam. N� de r�f. du vendeur 44784978

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Theory of Organic Reactions

Epiotis N. D.

Edit� par Springer, 2011

ISBN 10 : 3642668291 ISBN 13 : 9783642668296

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Theory of Organic Reactions

N. D. Epiotis

Edit� par Springer, Springer Gabler Okt 2011, 2011

ISBN 10 : 3642668291 ISBN 13 : 9783642668296

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Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -1. One-Determinental Theory of Chemical Reactivity.- 1.1 General Principles and Computational Schemes.- 1.2 Qualitative One-Determinental Models of Chemical Reactivity.- 1.3 The Static One Electron Molecular Orbital Model.- 1.4 Orbital Energies. The Donor-Acceptor Classification of Molecules and the Concept of Reaction Polarity.- 1.5 One Electron Interaction Matrix Elements and Overlap Integrals.- 1.6 The Woodward-Hoffmann Molecular Orbital Correlation Diagram.- 2. Configuration Interaction Overview of Chemical Reactivity.- 2.1 General Principles.- 2.2 Qualitative Configuration Interaction Models of Chemical Reactivity.- 2.3 The Static Linear Combination of Fragment Configurations Method.- 2.4 The Static Delocalized Configuration Interaction Method.- 2.5 The Dynamic Delocalized Configuration Interaction Method.- 3. The Dynamic Linear Combination of Fragment Configurations Method.- 3.1 Definitions.- 3.2 General Theoretical Considerations.- 3.3 The Interaction of Diabatic Surfaces.- 3.4 Polarity Control of Barrier Heights and Decay Efficiencies.- 3.5 The Effect of Excitation Energy on Photochemical Barrier Height.- 3.6 Diabatic Surface Interrelationships. A Classification of Chemical Reactions.- 4. Even-Even Intermodular Multicentric Reactions.- 4.1 Potential Energy Surfaces for 2 +2 Cycloadditions.- 4.2 The Effect of Polarity. Potential Energy Surfaces for Nonionic and Ionic In 2 +2 Cycloadditions.- 4.3 Pericyclic, Effectively Pericyclic and Quasipericyclic Reactions.- 4.4 The Effect of Unsymmetrical Substitution and the Effect of Conjugative Substitution.- 4.5 The Regiochemistry of 2 +2 Cycloadditions.- 4.6 Isomeric Reactions and the Topochemistry of 2 +2 Cycloreversions.- 4.7 The Topochemistry of Intramolecular Cycloadditions.- 4.8 The Selectivity-PolarityRelationship.- 4.9 Reaction Intermediates and Types of Organic Mechanisms.- 4.10 2 +2 Nonionic Photocycloadditions Involving n \* Excitation.- 4.11 The Effect of Low Lying Diexcited Diabatic Surfaces in Photoreactions.- 4.12 The Problem of Energy Wastage. The Concept of Dual Channel Photoreactions.- 4.13 Generalizations.- 5. The Problem of Correlation Imposed Barriers.- 6. Reactivity Trends of Thermal Cycloadditions.- 6.1 Introduction.- 6.2 Mechanisms of Stereochemical Nonretention in Cycloadditions.- 6.3 Reactivity Trends of Thermal Nonionic 2 +2 Cycloadditions.- 6.4 Reactivity Trends of Thermal Ionic 2 +2 Cycloadditions.- 6.5 The 2 +2 Ionic Cycloaddition Problem.- 6.6 Reactivity Trends of Thermal Nonionic 4 +2 Cycloadditions.- 6.7 Reactivity Trends of Thermal Ionic 4 +2 Cycloadditions.- 7. Reactivity Trends of Singlet Photochemical Cycloadditions.- 7.1 Introduction.- 7.2 The Chorochemistry of Singlet 2 +2 Photocycloadditions.- 7.3 'Unusual' Head to Head vs. Head to Tail Regioselectivity of Photocycloadditions.- 7.4 n \* State Dual Channel Mechanisms of Polar Nonionic Carbonyl Photocycloadditions.- 7.5 \* State Dual Channel Mechanisms of Polar Nonionic Photocycloadditions.- 8. Miscellaneous Intermolecular Multicentric Reactions.- 8.1 Cycloadditions of Cumulene Systems.- 8.2 The Ene Reaction.- 8.3 1,3 Dipolar Cycloadditions.- 9. A ddition Reactions.- 9.1 Introduction.- 9.2 Potential Energy Surfaces for 2 +2 Additions.- 9.3 Reactivity Trends of 2 +2 Additions.- 10. Even-Odd Multicentric Intermolecular Reactions.- 10.1 Potential Energy Surfaces for 2 +1 Cycloadditions.- 10.2 Reactivity Trends of Cationic Even-Odd Retro-Cycloadditions and Eliminations.- 11. Potential Energy Surfaces for Odd-Odd Multicentric IntermolecularReactions.- 12. Even-Even Intermolecular Bicentric Reactions.- 12.1 Potential Energy Surfaces for Electrophilic and Nucleophilic Additions.- 12.2 Reactivity Trends of Electrophilic and Nucleophilic Substitutions.- 13. Even-Odd Intermolecular Bicentric Reactions.- 13.1 Potential Energy Surfaces for Radical Additions.- 13.2 Reactivity Trends of Radical Substitution Reactions.- 14. Odd-Odd Intermolec. N� de r�f. du vendeur 9783642668296

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Theory of Organic Reactions (Reactivity and Structure: Concepts in Organic Chemistry)

N. D. Epiotis

Edit� par Springer Berlin Heidelberg, 2011

ISBN 10 : 3642668291 ISBN 13 : 9783642668296

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Theory of Organic Reactions

N. D. Epiotis

Edit� par Springer Berlin Heidelberg, 2011

ISBN 10 : 3642668291 ISBN 13 : 9783642668296

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Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne

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Taschenbuch. Etat : Neu. Druck auf Anfrage Neuware - Printed after ordering - Inhaltsangabe1. One-Determinental Theory of Chemical Reactivity.- 1.1 General Principles and Computational Schemes.- 1.2 Qualitative One-Determinental Models of Chemical Reactivity.- 1.3 The Static One Electron Molecular Orbital Model.- 1.4 Orbital Energies. The Donor-Acceptor Classification of Molecules and the Concept of Reaction Polarity.- 1.5 One Electron Interaction Matrix Elements and Overlap Integrals.- 1.6 The Woodward-Hoffmann Molecular Orbital Correlation Diagram.- 2. Configuration Interaction Overview of Chemical Reactivity.- 2.1 General Principles.- 2.2 Qualitative Configuration Interaction Models of Chemical Reactivity.- 2.3 The Static Linear Combination of Fragment Configurations Method.- 2.4 The Static Delocalized Configuration Interaction Method.- 2.5 The Dynamic Delocalized Configuration Interaction Method.- 3. The Dynamic Linear Combination of Fragment Configurations Method.- 3.1 Definitions.- 3.2 General Theoretical Considerations.- 3.3 The Interaction of Diabatic Surfaces.- 3.4 Polarity Control of Barrier Heights and Decay Efficiencies.- 3.5 The Effect of Excitation Energy on Photochemical Barrier Height.- 3.6 Diabatic Surface Interrelationships. A Classification of Chemical Reactions.- 4. Even-Even Intermodular Multicentric Reactions.- 4.1 Potential Energy Surfaces for 2 +2 Cycloadditions.- 4.2 The Effect of Polarity. Potential Energy Surfaces for Nonionic and Ionic In 2 +2 Cycloadditions.- 4.3 Pericyclic, Effectively Pericyclic and Quasipericyclic Reactions.- 4.4 The Effect of Unsymmetrical Substitution and the Effect of Conjugative Substitution.- 4.5 The Regiochemistry of 2 +2 Cycloadditions.- 4.6 Isomeric Reactions and the Topochemistry of 2 +2 Cycloreversions.- 4.7 The Topochemistry of Intramolecular Cycloadditions.- 4.8 The Selectivity-Polarity Relationship.- 4.9 Reaction Intermediates and Types of Organic Mechanisms.- 4.10 2 +2 Nonionic Photocycloadditions Involving n \* Excitation.- 4.11 The Effect of Low Lying Diexcited Diabatic Surfaces in Photoreactions.- 4.12 The Problem of Energy Wastage. The Concept of Dual Channel Photoreactions.- 4.13 Generalizations.- 5. The Problem of Correlation Imposed Barriers.- 6. Reactivity Trends of Thermal Cycloadditions.- 6.1 Introduction.- 6.2 Mechanisms of Stereochemical Nonretention in Cycloadditions.- 6.3 Reactivity Trends of Thermal Nonionic 2 +2 Cycloadditions.- 6.4 Reactivity Trends of Thermal Ionic 2 +2 Cycloadditions.- 6.5 The 2 +2 Ionic Cycloaddition Problem.- 6.6 Reactivity Trends of Thermal Nonionic 4 +2 Cycloadditions.- 6.7 Reactivity Trends of Thermal Ionic 4 +2 Cycloadditions.- 7. Reactivity Trends of Singlet Photochemical Cycloadditions.- 7.1 Introduction.- 7.2 The Chorochemistry of Singlet 2 +2 Photocycloadditions.- 7.3 'Unusual' Head to Head vs. Head to Tail Regioselectivity of Photocycloadditions.- 7.4 n \* State Dual Channel Mechanisms of Polar Nonionic Carbonyl Photocycloadditions.- 7.5 \* State Dual Channel Mechanisms of Polar Nonionic Photocycloadditions.- 8. Miscellaneous Intermolecular Multicentric Reactions.- 8.1 Cycloadditions of Cumulene Systems.- 8.2 The Ene Reaction.- 8.3 1,3 Dipolar Cycloadditions.- 9. A ddition Reactions.- 9.1 Introduction.- 9.2 Potential Energy Surfaces for 2 +2 Additions.- 9.3 Reactivity Trends of 2 +2 Additions.- 10. Even-Odd Multicentric Intermolecular Reactions.- 10.1 Potential Energy Surfaces for 2 +1 Cycloadditions.- 10.2 Reactivity Trends of Cationic Even-Odd Retro-Cycloadditions and Eliminations.- 11. Potential Energy Surfaces for Odd-Odd Multicentric Intermolecular Reactions.- 12. Even-Even Intermolecular Bicentric Reactions.- 12.1 Potential Energy Surfaces for Electrophilic and Nucleophilic Additions.- 12.2 Reactivity Trends of Electrophilic and Nucleophilic Substitutions.- 13. Even-Odd Intermolecular Bicentric Reactions.- 13.1 Potential Energy Surfaces for Radical Additions.- 13.2 Reactivity Trends of Radical Substitution Reactions.- 14. Odd-Odd Intermo. N� de r�f. du vendeur 9783642668296

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