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Organic chemistry / Robert Thornton Morrison, Robert Neilson Boyd
| Organic chemistry / Robert Thornton Morrison, Robert Neilson Boyd |
| Autore | Morrison, Robert Thornton |
| Edizione | [6th ed] |
| Descrizione fisica | XXVI, 1325 p. : ill.; 25 cm |
| Disciplina | 547 |
| Soggetto non controllato | chimica organica - manuali |
| ISBN | 0-13-630179-7 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNISA-990000262370203316 |
Morrison, Robert Thornton
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| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
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Organic chemistry / Robert Thornton Morrison, Robert Neilsen Boyd
| Organic chemistry / Robert Thornton Morrison, Robert Neilsen Boyd |
| Autore | Morrison, Robert Thornton |
| Edizione | [6th ed.] |
| Pubbl/distr/stampa | Englewood, Cliffs, N.J. : Prentice Hall, c1992 |
| Descrizione fisica | xxvi, 1279 p. : ill. (some col.) ; 26 cm |
| Disciplina | 547 |
| Altri autori (Persone) | Boyd, Robert Neilson |
| Soggetto topico | Chemistry, Organic |
| ISBN | 0136301797 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNISALENTO-991003533129707536 |
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Morrison, Robert Thornton
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| Englewood, Cliffs, N.J. : Prentice Hall, c1992 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. del Salento | ||
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Organic chemistry / Robert Thornton Morrison, Robert Neilson Boyd
| Organic chemistry / Robert Thornton Morrison, Robert Neilson Boyd |
| Autore | Morrison, Robert Thornton |
| Edizione | [5th ed.] |
| Pubbl/distr/stampa | Boston : Allyn and Bacon, c1987 |
| Descrizione fisica | xxxii, 1434 p. : ill. (some col.) ; 27 cm |
| Disciplina | 547 |
| Altri autori (Persone) | Boyd, Robert Neilsonauthor |
| Soggetto topico | Chemistry, Organic |
| ISBN | 0205084532 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNISALENTO-991003985969707536 |
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Morrison, Robert Thornton
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| Boston : Allyn and Bacon, c1987 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. del Salento | ||
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Organic chemistry : structure, mechanism, and synthesis / / Robert J. Ouellette and J. David Rawn
| Organic chemistry : structure, mechanism, and synthesis / / Robert J. Ouellette and J. David Rawn |
| Autore | Ouellette Robert J. <1938-> |
| Pubbl/distr/stampa | San Diego, California ; ; Waltham, Maryland : , : Elsevier, , 2014 |
| Descrizione fisica | 1 online resource (1241 p.) |
| Disciplina | 547 |
| Soggetto topico | Chemistry, Organic |
| Soggetto genere / forma | Electronic books. |
| ISBN | 0-12-801082-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Front Cover; Organic Chemistry:Structure, Mechanism, and Synthesis; Copyright; Dedication; Contents; Acknowledgments; Preface; Chapter 1: Structure and Bonding in Organic Compounds; 1.1 Brief Review of Atomic Structure; 1.2 Atomic Properties; 1.3 Ionic and Covalent Bonds; 1.4 Strategies for Writing Lewis Structures; 1.5 Formal Charge; 1.6 Molecular Geometry; 1.7 Resonance Structures; 1.8 Valence Shell Electron Pair Repulsion Theory; 1.9 Dipole Moments; 1.10 Molecular Orbital Theory; 1.11 The Hydrogen Molecule; 1.12 Bonding in Carbon Compounds; 1.13 SP3 Hybridization of Carbon in Methane
1.14 SP3 Hybridization of Carbon in Ethane1.15 SP2 Hybridization of Carbon in Ethene; 1.16 SP Hybridization of Carbon in Ethyne; 1.17 Effect of Hybridization on Bond Length and Bond Strength; 1.18 Hybridization of Nitrogen; 1.19 Hybridization of Oxygen; Exercises; Chapter 2 : Part I: Functional Groups and Their Properties; 2.1 Introduction to Functional Groups: Hydrocarbons and Haloalkanes; 2.2 Functional Groups that Contain Oxygen; 2.3 Functional Groups that Contain Nitrogen; 2.4 Functional Groups that Contain Sulfur; 2.5 Structural Formulas; 2.6 Bond-Line Structures; 2.7 Isomers Part II: Identification of Functional Groups by Infrared Spectroscopy2.8 Spectroscopy; 2.9 Infrared Spectroscopy; 2.10 Identifying Hydrocarbons; 2.11 Identifying Oxygen-Containing Compounds; 2.12 Identifying Nitrogen-Containing Compounds; 2.13 Bending Deformations; End-of-Chapter Exercises; Chapter 3: Introduction to Organic Reaction Mechanisms; 3.1 Acid-Base Reactions; 3.2 Chemical Equilibrium and Equilibrium Constants; 3.3 PH and PK Values; 3.4 Effect of Structure on Acidity; 3.5 Standard Free Energy Changes in Chemical Reactions; 3.6 Enthalpy Changes in Chemical Reactions 3.7 Bond Dissociation Energies3.8 Introduction to Reaction Mechanisms; 3.9 Structures and Stabilities of Carbon Radicals, Carbocations, and Carbanions; 3.10 Factors that Influence Reaction Rates; 3.11 Reaction Rate Theory; 3.12 Stability and Reactivity; End-of-Chapter Exercises; Chapter 4: Alkanes and Cycloalkanes: Structures and Reactions; 4.1 Classes of Hydrocarbons; 4.2 Alkanes; 4.3 Nomenclature of Alkanes; 4.4 Conformations of Alkanes; 4.5 Cycloalkanes; 4.6 Conformations of Cycloalkanes; 4.7 Conformational Mobility of Cyclohexane; 4.8 Monosubstituted Cyclohexanes 4.9 Disubstituted Cyclohexanes4.10 Polycyclic Molecules; 4.11 Physical Properties of Alkanes; 4.12 Stabilities of Alkyl Radicals; 4.13 Chlorination of an Alkane-A Radical Reaction; Exercises; Chapter 5: Alkenes Structures and Properties; 5.1 Alkenes; 5.2 Structure and Bonding of Alkenes; 5.3 Unsaturation Number; 5.4 Geometric Isomerism; 5.5 E,Z Nomenclature of Geometrical Isomers; 5.6 Nomenclature of Alkenes; 5.7 Physical Properties of Alkenes; 5.8 Stability of Alkenes; 5.9 Reduction of Alkenes; 5.10 Mechanism of Catalytic Hydrogenation; 5.11 Heats of Hydrogenation of Alkenes; Exercises Chapter 6: Alkenes: Addition Reactions |
| Record Nr. | UNINA-9910465173503321 |
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Ouellette Robert J. <1938->
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| San Diego, California ; ; Waltham, Maryland : , : Elsevier, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Organic chemistry : structure, mechanism, and synthesis / / Robert J. Ouellette and J. David Rawn
| Organic chemistry : structure, mechanism, and synthesis / / Robert J. Ouellette and J. David Rawn |
| Autore | Ouellette Robert J. <1938-> |
| Pubbl/distr/stampa | San Diego, California ; ; Waltham, Maryland : , : Elsevier, , 2014 |
| Descrizione fisica | 1 online resource (1241 p.) |
| Disciplina | 547 |
| Soggetto topico | Chemistry, Organic |
| ISBN | 0-12-801082-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Front Cover; Organic Chemistry:Structure, Mechanism, and Synthesis; Copyright; Dedication; Contents; Acknowledgments; Preface; Chapter 1: Structure and Bonding in Organic Compounds; 1.1 Brief Review of Atomic Structure; 1.2 Atomic Properties; 1.3 Ionic and Covalent Bonds; 1.4 Strategies for Writing Lewis Structures; 1.5 Formal Charge; 1.6 Molecular Geometry; 1.7 Resonance Structures; 1.8 Valence Shell Electron Pair Repulsion Theory; 1.9 Dipole Moments; 1.10 Molecular Orbital Theory; 1.11 The Hydrogen Molecule; 1.12 Bonding in Carbon Compounds; 1.13 SP3 Hybridization of Carbon in Methane
1.14 SP3 Hybridization of Carbon in Ethane1.15 SP2 Hybridization of Carbon in Ethene; 1.16 SP Hybridization of Carbon in Ethyne; 1.17 Effect of Hybridization on Bond Length and Bond Strength; 1.18 Hybridization of Nitrogen; 1.19 Hybridization of Oxygen; Exercises; Chapter 2 : Part I: Functional Groups and Their Properties; 2.1 Introduction to Functional Groups: Hydrocarbons and Haloalkanes; 2.2 Functional Groups that Contain Oxygen; 2.3 Functional Groups that Contain Nitrogen; 2.4 Functional Groups that Contain Sulfur; 2.5 Structural Formulas; 2.6 Bond-Line Structures; 2.7 Isomers Part II: Identification of Functional Groups by Infrared Spectroscopy2.8 Spectroscopy; 2.9 Infrared Spectroscopy; 2.10 Identifying Hydrocarbons; 2.11 Identifying Oxygen-Containing Compounds; 2.12 Identifying Nitrogen-Containing Compounds; 2.13 Bending Deformations; End-of-Chapter Exercises; Chapter 3: Introduction to Organic Reaction Mechanisms; 3.1 Acid-Base Reactions; 3.2 Chemical Equilibrium and Equilibrium Constants; 3.3 PH and PK Values; 3.4 Effect of Structure on Acidity; 3.5 Standard Free Energy Changes in Chemical Reactions; 3.6 Enthalpy Changes in Chemical Reactions 3.7 Bond Dissociation Energies3.8 Introduction to Reaction Mechanisms; 3.9 Structures and Stabilities of Carbon Radicals, Carbocations, and Carbanions; 3.10 Factors that Influence Reaction Rates; 3.11 Reaction Rate Theory; 3.12 Stability and Reactivity; End-of-Chapter Exercises; Chapter 4: Alkanes and Cycloalkanes: Structures and Reactions; 4.1 Classes of Hydrocarbons; 4.2 Alkanes; 4.3 Nomenclature of Alkanes; 4.4 Conformations of Alkanes; 4.5 Cycloalkanes; 4.6 Conformations of Cycloalkanes; 4.7 Conformational Mobility of Cyclohexane; 4.8 Monosubstituted Cyclohexanes 4.9 Disubstituted Cyclohexanes4.10 Polycyclic Molecules; 4.11 Physical Properties of Alkanes; 4.12 Stabilities of Alkyl Radicals; 4.13 Chlorination of an Alkane-A Radical Reaction; Exercises; Chapter 5: Alkenes Structures and Properties; 5.1 Alkenes; 5.2 Structure and Bonding of Alkenes; 5.3 Unsaturation Number; 5.4 Geometric Isomerism; 5.5 E,Z Nomenclature of Geometrical Isomers; 5.6 Nomenclature of Alkenes; 5.7 Physical Properties of Alkenes; 5.8 Stability of Alkenes; 5.9 Reduction of Alkenes; 5.10 Mechanism of Catalytic Hydrogenation; 5.11 Heats of Hydrogenation of Alkenes; Exercises Chapter 6: Alkenes: Addition Reactions |
| Record Nr. | UNINA-9910792292203321 |
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Ouellette Robert J. <1938->
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| San Diego, California ; ; Waltham, Maryland : , : Elsevier, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Organic chemistry : structure, mechanism, and synthesis / / Robert J. Ouellette and J. David Rawn
| Organic chemistry : structure, mechanism, and synthesis / / Robert J. Ouellette and J. David Rawn |
| Autore | Ouellette Robert J. <1938-> |
| Pubbl/distr/stampa | San Diego, California ; ; Waltham, Maryland : , : Elsevier, , 2014 |
| Descrizione fisica | 1 online resource (1241 p.) |
| Disciplina | 547 |
| Soggetto topico | Chemistry, Organic |
| ISBN | 0-12-801082-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Front Cover; Organic Chemistry:Structure, Mechanism, and Synthesis; Copyright; Dedication; Contents; Acknowledgments; Preface; Chapter 1: Structure and Bonding in Organic Compounds; 1.1 Brief Review of Atomic Structure; 1.2 Atomic Properties; 1.3 Ionic and Covalent Bonds; 1.4 Strategies for Writing Lewis Structures; 1.5 Formal Charge; 1.6 Molecular Geometry; 1.7 Resonance Structures; 1.8 Valence Shell Electron Pair Repulsion Theory; 1.9 Dipole Moments; 1.10 Molecular Orbital Theory; 1.11 The Hydrogen Molecule; 1.12 Bonding in Carbon Compounds; 1.13 SP3 Hybridization of Carbon in Methane
1.14 SP3 Hybridization of Carbon in Ethane1.15 SP2 Hybridization of Carbon in Ethene; 1.16 SP Hybridization of Carbon in Ethyne; 1.17 Effect of Hybridization on Bond Length and Bond Strength; 1.18 Hybridization of Nitrogen; 1.19 Hybridization of Oxygen; Exercises; Chapter 2 : Part I: Functional Groups and Their Properties; 2.1 Introduction to Functional Groups: Hydrocarbons and Haloalkanes; 2.2 Functional Groups that Contain Oxygen; 2.3 Functional Groups that Contain Nitrogen; 2.4 Functional Groups that Contain Sulfur; 2.5 Structural Formulas; 2.6 Bond-Line Structures; 2.7 Isomers Part II: Identification of Functional Groups by Infrared Spectroscopy2.8 Spectroscopy; 2.9 Infrared Spectroscopy; 2.10 Identifying Hydrocarbons; 2.11 Identifying Oxygen-Containing Compounds; 2.12 Identifying Nitrogen-Containing Compounds; 2.13 Bending Deformations; End-of-Chapter Exercises; Chapter 3: Introduction to Organic Reaction Mechanisms; 3.1 Acid-Base Reactions; 3.2 Chemical Equilibrium and Equilibrium Constants; 3.3 PH and PK Values; 3.4 Effect of Structure on Acidity; 3.5 Standard Free Energy Changes in Chemical Reactions; 3.6 Enthalpy Changes in Chemical Reactions 3.7 Bond Dissociation Energies3.8 Introduction to Reaction Mechanisms; 3.9 Structures and Stabilities of Carbon Radicals, Carbocations, and Carbanions; 3.10 Factors that Influence Reaction Rates; 3.11 Reaction Rate Theory; 3.12 Stability and Reactivity; End-of-Chapter Exercises; Chapter 4: Alkanes and Cycloalkanes: Structures and Reactions; 4.1 Classes of Hydrocarbons; 4.2 Alkanes; 4.3 Nomenclature of Alkanes; 4.4 Conformations of Alkanes; 4.5 Cycloalkanes; 4.6 Conformations of Cycloalkanes; 4.7 Conformational Mobility of Cyclohexane; 4.8 Monosubstituted Cyclohexanes 4.9 Disubstituted Cyclohexanes4.10 Polycyclic Molecules; 4.11 Physical Properties of Alkanes; 4.12 Stabilities of Alkyl Radicals; 4.13 Chlorination of an Alkane-A Radical Reaction; Exercises; Chapter 5: Alkenes Structures and Properties; 5.1 Alkenes; 5.2 Structure and Bonding of Alkenes; 5.3 Unsaturation Number; 5.4 Geometric Isomerism; 5.5 E,Z Nomenclature of Geometrical Isomers; 5.6 Nomenclature of Alkenes; 5.7 Physical Properties of Alkenes; 5.8 Stability of Alkenes; 5.9 Reduction of Alkenes; 5.10 Mechanism of Catalytic Hydrogenation; 5.11 Heats of Hydrogenation of Alkenes; Exercises Chapter 6: Alkenes: Addition Reactions |
| Record Nr. | UNINA-9910808337003321 |
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Ouellette Robert J. <1938->
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| San Diego, California ; ; Waltham, Maryland : , : Elsevier, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Organic chemistry / / G. L. Patrick
| Organic chemistry / / G. L. Patrick |
| Autore | Patrick Graham L. |
| Edizione | [Second edition.] |
| Pubbl/distr/stampa | New York, New York ; ; London, [England] : , : Garland Science, , 2012 |
| Descrizione fisica | 1 online resource (362 p.) |
| Disciplina | 547 |
| Collana | BIOS Instant Notes |
| Soggetto topico | Chemistry, Organic |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-09924-0
9786610099245 0-203-42761-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title Page; Table of Contents; Preface; Section A - Structure and bonding; A1 Atomic structure of carbon; A2 Covalent bonding and hybridization; A3 sp3 Hybridization; A4 sp2 Hybridization; A5 sp Hybridization; A6 Bonds and hybridized centers; Section B - Alkanes and cycloalkanes; B1 Definition; B2 Drawing structures; B3 Nomenclature; Section C - Functional groups; C1 Recognition of functional groups; C2 Aliphatic and aromatic functional groups; C3 Intermolecular bonding; C4 Properties and reactions; C5 Nomenclature of compounds with functional groups
C6 Primary, secondary, tertiary and quaternary nomenclatureSection D - Stereochemistry; D1 Constitutional isomers; D2 Configurational isomers - alkenes and cycloalkanes; D3 Configurational isomers - optical isomers; D4 Conformational isomers; Section E - Nucleophiles and electrophiles; E1 Definition; E2 Charged species; E3 Neutral inorganic species; E4 Organic structures; Section F - Reactions and mechanisms; F1 Reactions; F2 Mechanisms; Section G - Acid-base reactions; G1 Brønsted-Lowry acids and bases; G2 Acid strength; G3 Base strength; G4 Lewis acids and bases; G5 Enolates Section H - Alkenes and alkynesH1 Preparation of alkenes and alkynes; H2 Properties of alkenes and alkynes; H3 Electrophilic addition to symmetrical alkenes; H4 Electrophilic addition to unsymmetrical alkenes; H5 Carbocation stabilization; H6 Reduction and oxidation of alkenes; H7 Hydroboration of alkenes; H8 Electrophilic additions to alkynes; H9 Reduction of alkynes; H10 Alkylation of terminal alkynes; H11 Conjugated dienes; Section I - Aromatic chemistry; I1 Aromaticity; I2 Preparation and properties; I3 Electrophilic substitutions of benzene; I4 Synthesis of monosubstituted aromatic rings I5 Electrophilic substitutions of monosubstituted aromatic ringsI6 Synthesis of di- and trisubstituted aromatic rings; I7 Oxidation and reduction; Section J - Aldehydes and ketones; J1 Preparation; J2 Properties; J3 Nucleophilic addition; J4 Nucleophilic addition - charged nucleophiles; J5 Electronic and steric effects; J6 Nucleophilic addition - nitrogen nucleophiles; J7 Nucleophilic addition - oxygen and sulfur nucleophiles; J8 Reactions of enolate ions; J9 α-Halogenation; J10 Reduction and oxidation; J11 α,β-Unsaturated aldehydes and ketones Section K - Carboxylic acids and carboxylic acid derivativesK1 Structure and properties; K2 Nucleophilic substitution; K3 Reactivity; K4 Preparations of carboxylic acids; K5 Preparations of carboxylic acid derivatives; K6 Reactions; K7 Enolate reactions; Section L - Alkyl halides; L1 Preparation and physical properties of alkyl halides; L2 Nucleophilic substitution; L3 Factors affecting SN2 versus SN1 reactions; L4 Elimination; L5 Elimination versus substitution; L6 Reactions of alkyl halides; L7 Organometallic reactions; Section M - Alcohols, phenols, and thiols; M1 Preparation of alcohols M2 Preparation of phenols |
| Record Nr. | UNINA-9910450784603321 |
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Patrick Graham L.
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| New York, New York ; ; London, [England] : , : Garland Science, , 2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Organic chemistry / / G.L. Patrick
| Organic chemistry / / G.L. Patrick |
| Autore | Patrick Graham L |
| Edizione | [Second edition.] |
| Pubbl/distr/stampa | [Place of publication not identified], : CRC Press, 2003 |
| Descrizione fisica | 1 online resource (362 p.) |
| Disciplina | 547 |
| Collana | BIOS Instant Notes |
| Soggetto topico | Chemistry, Organic |
| ISBN |
1-280-09924-0
9786610099245 0-203-42761-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title Page; Table of Contents; Preface; Section A - Structure and bonding; A1 Atomic structure of carbon; A2 Covalent bonding and hybridization; A3 sp3 Hybridization; A4 sp2 Hybridization; A5 sp Hybridization; A6 Bonds and hybridized centers; Section B - Alkanes and cycloalkanes; B1 Definition; B2 Drawing structures; B3 Nomenclature; Section C - Functional groups; C1 Recognition of functional groups; C2 Aliphatic and aromatic functional groups; C3 Intermolecular bonding; C4 Properties and reactions; C5 Nomenclature of compounds with functional groups
C6 Primary, secondary, tertiary and quaternary nomenclatureSection D - Stereochemistry; D1 Constitutional isomers; D2 Configurational isomers - alkenes and cycloalkanes; D3 Configurational isomers - optical isomers; D4 Conformational isomers; Section E - Nucleophiles and electrophiles; E1 Definition; E2 Charged species; E3 Neutral inorganic species; E4 Organic structures; Section F - Reactions and mechanisms; F1 Reactions; F2 Mechanisms; Section G - Acid-base reactions; G1 Brønsted-Lowry acids and bases; G2 Acid strength; G3 Base strength; G4 Lewis acids and bases; G5 Enolates Section H - Alkenes and alkynesH1 Preparation of alkenes and alkynes; H2 Properties of alkenes and alkynes; H3 Electrophilic addition to symmetrical alkenes; H4 Electrophilic addition to unsymmetrical alkenes; H5 Carbocation stabilization; H6 Reduction and oxidation of alkenes; H7 Hydroboration of alkenes; H8 Electrophilic additions to alkynes; H9 Reduction of alkynes; H10 Alkylation of terminal alkynes; H11 Conjugated dienes; Section I - Aromatic chemistry; I1 Aromaticity; I2 Preparation and properties; I3 Electrophilic substitutions of benzene; I4 Synthesis of monosubstituted aromatic rings I5 Electrophilic substitutions of monosubstituted aromatic ringsI6 Synthesis of di- and trisubstituted aromatic rings; I7 Oxidation and reduction; Section J - Aldehydes and ketones; J1 Preparation; J2 Properties; J3 Nucleophilic addition; J4 Nucleophilic addition - charged nucleophiles; J5 Electronic and steric effects; J6 Nucleophilic addition - nitrogen nucleophiles; J7 Nucleophilic addition - oxygen and sulfur nucleophiles; J8 Reactions of enolate ions; J9 α-Halogenation; J10 Reduction and oxidation; J11 α,β-Unsaturated aldehydes and ketones Section K - Carboxylic acids and carboxylic acid derivativesK1 Structure and properties; K2 Nucleophilic substitution; K3 Reactivity; K4 Preparations of carboxylic acids; K5 Preparations of carboxylic acid derivatives; K6 Reactions; K7 Enolate reactions; Section L - Alkyl halides; L1 Preparation and physical properties of alkyl halides; L2 Nucleophilic substitution; L3 Factors affecting SN2 versus SN1 reactions; L4 Elimination; L5 Elimination versus substitution; L6 Reactions of alkyl halides; L7 Organometallic reactions; Section M - Alcohols, phenols, and thiols; M1 Preparation of alcohols M2 Preparation of phenols |
| Record Nr. | UNINA-9910783882103321 |
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Patrick Graham L
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| [Place of publication not identified], : CRC Press, 2003 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Organic chemistry / / G.L. Patrick
| Organic chemistry / / G.L. Patrick |
| Autore | Patrick Graham L |
| Edizione | [Second edition.] |
| Pubbl/distr/stampa | [Place of publication not identified], : CRC Press, 2003 |
| Descrizione fisica | 1 online resource (362 p.) |
| Disciplina | 547 |
| Collana | BIOS Instant Notes |
| Soggetto topico | Chemistry, Organic |
| ISBN |
1-280-09924-0
9786610099245 0-203-42761-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title Page; Table of Contents; Preface; Section A - Structure and bonding; A1 Atomic structure of carbon; A2 Covalent bonding and hybridization; A3 sp3 Hybridization; A4 sp2 Hybridization; A5 sp Hybridization; A6 Bonds and hybridized centers; Section B - Alkanes and cycloalkanes; B1 Definition; B2 Drawing structures; B3 Nomenclature; Section C - Functional groups; C1 Recognition of functional groups; C2 Aliphatic and aromatic functional groups; C3 Intermolecular bonding; C4 Properties and reactions; C5 Nomenclature of compounds with functional groups
C6 Primary, secondary, tertiary and quaternary nomenclatureSection D - Stereochemistry; D1 Constitutional isomers; D2 Configurational isomers - alkenes and cycloalkanes; D3 Configurational isomers - optical isomers; D4 Conformational isomers; Section E - Nucleophiles and electrophiles; E1 Definition; E2 Charged species; E3 Neutral inorganic species; E4 Organic structures; Section F - Reactions and mechanisms; F1 Reactions; F2 Mechanisms; Section G - Acid-base reactions; G1 Brønsted-Lowry acids and bases; G2 Acid strength; G3 Base strength; G4 Lewis acids and bases; G5 Enolates Section H - Alkenes and alkynesH1 Preparation of alkenes and alkynes; H2 Properties of alkenes and alkynes; H3 Electrophilic addition to symmetrical alkenes; H4 Electrophilic addition to unsymmetrical alkenes; H5 Carbocation stabilization; H6 Reduction and oxidation of alkenes; H7 Hydroboration of alkenes; H8 Electrophilic additions to alkynes; H9 Reduction of alkynes; H10 Alkylation of terminal alkynes; H11 Conjugated dienes; Section I - Aromatic chemistry; I1 Aromaticity; I2 Preparation and properties; I3 Electrophilic substitutions of benzene; I4 Synthesis of monosubstituted aromatic rings I5 Electrophilic substitutions of monosubstituted aromatic ringsI6 Synthesis of di- and trisubstituted aromatic rings; I7 Oxidation and reduction; Section J - Aldehydes and ketones; J1 Preparation; J2 Properties; J3 Nucleophilic addition; J4 Nucleophilic addition - charged nucleophiles; J5 Electronic and steric effects; J6 Nucleophilic addition - nitrogen nucleophiles; J7 Nucleophilic addition - oxygen and sulfur nucleophiles; J8 Reactions of enolate ions; J9 α-Halogenation; J10 Reduction and oxidation; J11 α,β-Unsaturated aldehydes and ketones Section K - Carboxylic acids and carboxylic acid derivativesK1 Structure and properties; K2 Nucleophilic substitution; K3 Reactivity; K4 Preparations of carboxylic acids; K5 Preparations of carboxylic acid derivatives; K6 Reactions; K7 Enolate reactions; Section L - Alkyl halides; L1 Preparation and physical properties of alkyl halides; L2 Nucleophilic substitution; L3 Factors affecting SN2 versus SN1 reactions; L4 Elimination; L5 Elimination versus substitution; L6 Reactions of alkyl halides; L7 Organometallic reactions; Section M - Alcohols, phenols, and thiols; M1 Preparation of alcohols M2 Preparation of phenols |
| Record Nr. | UNINA-9910814138303321 |
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Patrick Graham L
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| [Place of publication not identified], : CRC Press, 2003 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Organic chemistry : methane to macromolecules / (by) J. D. Roberts, R. Stewart, M. C. Caserio
| Organic chemistry : methane to macromolecules / (by) J. D. Roberts, R. Stewart, M. C. Caserio |
| Autore | Roberts, John D. |
| Pubbl/distr/stampa | New York, : Benjamin, 1971 |
| Descrizione fisica | XIV, 850 p. ; 24 cm. |
| Disciplina | 547(Chimica organica) |
| Altri autori (Persone) |
Caserio, Marjorie C.
Stewart, Ross |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNICAMPANIA-SUN0094750 |
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Roberts, John D.
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| New York, : Benjamin, 1971 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Vanvitelli | ||
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