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Essential organic chemistry / / Paula Yurkanis Bruice
| Essential organic chemistry / / Paula Yurkanis Bruice |
| Autore | Bruice Paula Yurkanis <1941-> |
| Edizione | [Third edition, global edition.] |
| Pubbl/distr/stampa | Harlow, England : , : Pearson, , 2016 |
| Descrizione fisica | 1 online resource (761 pages) : illustration (some color), tables |
| Disciplina | 547 |
| Collana | Always learning |
| Soggetto topico | Chemistry, Organic |
| ISBN | 1-292-08905-9 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover -- Title Page -- Copyright Page -- Brief Table of Contents -- Contents -- Preface -- About the Author -- Chapter 1 Remembering General Chemistry: Electronic Structure and Bonding -- Natural Organic Compounds Versus Synthetic Organic Compounds -- 1.1 The Structure of an Atom -- 1.2 How the Electrons in an Atom Are Distributed -- 1.3 Ionic and Covalent Bonds -- 1.4 How the Structure of a Compound Is Represented -- PROBLEM-SOLVING STRATEGY -- 1.5 Atomic Orbitals -- 1.6 How Atoms Form Covalent Bonds -- 1.7 How Single Bonds Are Formed in Organic Compounds -- 1.8 How a Double Bond Is Formed: The Bonds in Ethene -- Diamond, Graphite, Graphene, and Fullerenes: Substances that Contain Only Carbon Atoms -- 1.9 How a Triple Bond Is Formed: The Bonds in Ethyne -- 1.10 The Bonds in the Methyl Cation, the Methyl Radical, and the Methyl Anion -- 1.11 The Bonds in Ammonia and in the Ammonium Ion -- 1.12 The Bonds in Water -- Water-A Compound Central to Life -- 1.13 The Bond in a Hydrogen Halide -- 1.14 Summary: Hybridization, Bond Lengths, Bond Strengths, and Bond Angles -- PROBLEM-SOLVING STRATEGY -- 1.15 The Dipole Moments of Molecules -- SOME IMPORTANT THINGS TO REMEMBER -- PROBLEMS -- Chapter 2 Acids and Bases: Central to Understanding Organic Chemistry -- 2.1 An Introduction to Acids and Bases -- 2.2 pKa and pH -- Acid Rain -- 2.3 Organic Acids and Bases -- Poisonous Amines -- PROBLEM-SOLVING STRATEGY -- 2.4 How to Predict the Outcome of an Acid-Base Reaction -- 2.5 How to Determine the Position of Equilibrium -- 2.6 How the Structure of an Acid Affects Its pKa Value -- 2.7 How Substituents Affect the Strength of an Acid -- PROBLEM-SOLVING STRATEGY -- 2.8 An Introduction to Delocalized Electrons -- Fosamax Prevents Bones from Being Nibbled Away -- 2.9 A Summary of the Factors that Determine Acid Strength.
2.10 How pH Affects the Structure of an Organic Compound -- PROBLEM-SOLVING STRATEGY -- Aspirin Must Be in Its Basic Form to Be Physiologically Active -- 2.11 Buffer Solutions -- Blood: A Buffered Solution -- SOME IMPORTANT THINGS TO REMEMBER -- PROBLEMS -- TUTORIAL Acids and Bases -- Chapter 3 An Introduction to Organic Compounds -- 3.1 How Alkyl Substituents Are Named -- Bad-Smelling Compounds -- 3.2 The Nomenclature of Alkanes -- How is the Octane Number of Gasoline Determined? -- 3.3 The Nomenclature of Cycloalkanes Skeletal Structures -- PROBLEM-SOLVING STRATEGY -- 3.4 The Nomenclature of Alkyl Halides -- PROBLEM-SOLVING STRATEGY -- 3.5 The Classification of Alkyl Halides, Alcohols, and Amines -- Nitrosamines and Cancer -- 3.6 The Structures of Alkyl Halides, Alcohols, Ethers, and Amines -- 3.7 Noncovalent Interactions -- PROBLEM-SOLVING STRATEGY -- Drugs Bind to Their Receptors -- 3.8 Factors that Affect the Solubility of Organic Compounds -- Cell Membranes -- 3.9 Rotation Occurs About Carbon-Carbon Single Bonds -- 3.10 Some Cycloalkanes have Angle Strain -- Von Baeyer, Barbituric Acid, and Blue Jeans -- 3.11 Conformers of Cyclohexane -- 3.12 Conformers of Monosubstituted Cyclohexanes -- Starch and Cellulose-Axial and Equatorial -- 3.13 Conformers of Disubstituted Cyclohexanes -- PROBLEM-SOLVING STRATEGY -- 3.14 Fused Cyclohexane Rings -- Cholesterol and Heart Disease -- How High Cholesterol Is Treated Clinically -- SOME IMPORTANT THINGS TO REMEMBER -- PROBLEMS -- Chapter 4 Isomers: The Arrangement of Atoms in Space -- 4.1 CIS-Trans Isomers Result from Restricted Rotation -- Cis-Trans Interconversion in Vision -- 4.2 Designating Geometric Isomers Using the E,Z System -- PROBLEM-SOLVING STRATEGY -- 4.3 A Chiral Object Has a Nonsuperimposable Mirror Image -- 4.4 An Asymmetric Center Is a Cause of Chirality in a Molecule. 4.5 Isomers with One Asymmetric Center -- 4.6 How to Draw Enantiomers -- 4.7 Naming Enantiomers by the R,S System -- PROBLEM-SOLVING STRATEGY -- PROBLEM-SOLVING STRATEGY -- 4.8 Chiral Compounds Are Optically Active -- 4.9 How Specific Rotation Is Measured -- 4.10 Isomers with More than One Asymmetric Center -- 4.11 Stereoisomers of Cyclic Compounds -- PROBLEM-SOLVING STRATEGY -- 4.12 Meso Compounds Have Asymmetric Centers but Are Optically Inactive -- PROBLEM-SOLVING STRATEGY -- 4.13 Receptors -- The Enantiomers of Thalidomide -- 4.14 How Enantiomers Can Be Separated -- Chiral Drugs -- SOME IMPORTANT THINGS TO REMEMBER -- PROBLEMS -- Chapter 5 Alkenes -- Pheromones -- 5.1 The Nomenclature of Alkenes -- 5.2 How an Organic Compound Reacts Depends on its Functional Group -- 5.3 How Alkenes React . Curved Arrows Show the Flow of Electrons -- A Few Words About Curved Arrows -- 5.4 Thermodynamics: How Much Product Is Formed? -- 5.5 Increasing the Amount of Product Formed in a Reaction -- 5.6 Using ΔH° Values to Determine the Relative Stabilities of Alkenes -- PROBLEM-SOLVING STRATEGY -- Trans Fats -- 5.7 Kinetics: How Fast Is the Product Formed? -- 5.8 The Rate of a Chemical Reaction -- 5.9 The Reaction Coordinate Diagram for the Reaction of 2-Butene with HBr -- 5.10 Catalysis -- 5.11 Catalysis by Enzymes -- SOME IMPORTANT THINGS TO REMEMBER -- PROBLEMS -- TUTORIAL An Exercise in Drawing Curved Arrows: Pushing Electrons -- Chapter 6 The Reactions of Alkenes and Alkynes -- Green Chemistry: Aiming for Sustainability -- 6.1 The Addition of a Hydrogen Halide to an Alkene -- 6.2 Carbocation Stability Depends on the Number of Alkyl Groups Attached to the Positively Charged Carbon -- 6.3 Electrophilic Addition Reactions Are Regioselective -- Which Are More Harmful, Natural Pesticides or Synthetic Pesticides? -- PROBLEM-SOLVING STRATEGY. 6.4 A Carbocation will Rearrange if It Can Form a More Stable Carbocation -- 6.5 The Addition of Water to an Alkene -- 6.6 The Stereochemistry of Alkene Reactions -- PROBLEM-SOLVING STRATEGY -- 6.7 The Stereochemistry of Enzyme-Catalyzed Reactions -- 6.8 Enantiomers Can Be Distinguished by Biological Molecules -- 6.9 An Introduction to Alkynes -- Synthetic Alkynes Are Used to Treat Parkinson's Disease -- Why Are Drugs So Expensive? -- 6.10 The Nomenclature of Alkynes -- Synthetic Alkynes Are Used for Birth Control -- 6.11 The Structure of Alkynes -- 6.12 The Physical Properties of Unsaturated Hydrocarbons -- 6.13 The Addition of a Hydrogen Halide to an Alkyne -- 6.14 The Addition of Water to an Alkyne -- 6.15 The Addition of Hydrogen to an Alkyne -- SOME IMPORTANT THINGS TO REMEMBER -- SUMMARY OF REACTIONS -- PROBLEMS -- Chapter 7 Delocalized Electrons and Their Effect on Stability, pKa, and the Products of a Reaction Aromaticity and the Reactions of Benzene -- 7.1 Delocalized Electrons Explain Benzene's Structure -- Kekule's Dream -- 7.2 The Bonding in Benzene -- 7.3 Resonance Contributors and the Resonance Hybrid -- 7.4 How to Draw Resonance Contributors -- Electron Delocalization Affects the Three-Dimensional Shape of Proteins -- 7.5 The Predicted Stabilities of Resonance Contributors -- 7.6 Delocalization Energy Is the Additional Stability Delocalized Electrons Give to a Compound -- 7.7 Delocalized Electrons Increase Stability -- PROBLEM-SOLVING STRATEGY -- PROBLEM-SOLVING STRATEGY -- 7.8 Delocalized Electrons Affect pKa Values -- PROBLEM-SOLVING STRATEGY -- 7.9 Electronic Effects -- 7.10 Delocalized Electrons Can Affect the Product of a Reaction -- 7.11 Reactions of Dienes -- 7.12 The Diels-Alder Reaction Is a 1, 4-Addition Reaction -- 7.13 Benzene Is an Aromatic Compound -- 7.14 The Two Criteria for Aromaticity. 7.15 Applying the Criteria for Aromaticity -- Buckyballs -- 7.16 How Benzene Reacts -- 7.17 The Mechanism for Electrophilic Aromatic Substitution Reactions -- Thyroxine -- 7.18 Organizing What We Know About the Reactions of Organic Compounds -- SOME IMPORTANT THINGS TO REMEMBER -- SUMMARY OF REACTIONS -- PROBLEMS -- TUTORIAL: DRAWING RESONANCE CONTRIBUTORS -- Chapter 8 Substitution and Elimination Reactions of Alkyl Halides -- DDT: A Synthetic Organohalide That Kills Disease-Spreading Insects -- 8.1 The Mechanism for an SN2 Reaction -- 8.2 Factors That Affect SN2 Reactions -- Why Are Living Organisms Composed of Carbon Instead of Silicon? -- 8.3 The Mechanism for an SN1 Reaction -- 8.4 Factors That Affect SN1 Reactions -- 8.5 Comparing SN2 and SN1 Reactions -- PROBLEM-SOLVING STRATEGY -- Naturally Occurring Organohalides That Defend against Predators -- 8.6 Intermolecular versus Intramolecular Reactions -- PROBLEM-SOLVING STRATEGY -- 8.7 Elimination Reactions of Alkyl Halides -- 8.8 The Products of an Elimination Reaction -- 8.9 Relative Reactivities of Alkyl Halides Reactions -- The Nobel Prize -- 8.10 Does a Tertiary Alkyl Halide Undergo SN2/E2 Reactions or SN1/E1 Reactions? -- 8.11 Competition between Substitution and Elimination -- 8.12 Solvent Effects -- Solvation Efects -- 8.13 Substitution Reactions in Synthesis -- SOME IMPORTANT THINGS TO REMEMBER -- SUMMARY OF REACTIONS -- PROBLEMS -- Chapter 9 Reactions of Alcohols, Ethers, Epoxides, Amines, and Thiols -- 9.1 The Nomenclature of Alcohols -- Grain Alcohol and Wood Alcohol -- 9.2 Activating an Alcohol for Nucleophilic Substitution by Protonation -- 9.3 Activating an OH Group for Nucleophilic Substitution in a Cell -- The Inability to Perform an SN2 Reaction Causes a Severe Clinical Disorder -- 9.4 Elimination Reactions of Alcohols: Dehydration -- 9.5 Oxidation of Alcohols. Blood Alcohol Content. |
| Record Nr. | UNINA-9910154958003321 |
Bruice Paula Yurkanis <1941->
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| Harlow, England : , : Pearson, , 2016 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Organic chemistry / / Paula Yurkanis Bruice
| Organic chemistry / / Paula Yurkanis Bruice |
| Autore | Bruice Paula Yurkanis <1941-> |
| Edizione | [Eighth edition, Global edition.] |
| Pubbl/distr/stampa | Harlow, England : , : Pearson, , [2017] |
| Descrizione fisica | 1 online resource (1,339 pages) : colour illustrations, photographs |
| Disciplina | 547 |
| Soggetto topico |
Chemistry, Organic
Química orgànica |
| ISBN |
9781292160351
9781292160344 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover -- Title Page -- Copyright Page -- Preface -- ACKNOWLEDGMENTS -- About the Author -- Contents -- PART ONE: An Introduction to the Study of Organic Chemistry -- 1 Remembering General Chemistry: Electronic Structure and Bonding -- CHEMICAL CONNECTION: Natural versus Synthetic Organic Compounds -- 1.1 The Structure of an Atom -- 1.2 How the Electrons in an Atom are Distributed -- 1.3 Covalent Bonds -- 1.4 How the Structure of a Compound is Represented -- PROBLEM-SOLVING STRATEGY -- 1.5 Atomic Orbitals -- 1.6 An Introduction to Molecular Orbital Theory -- 1.7 How Single Bonds are Formed in Organic Compounds -- 1.8 How a Double Bond is Formed: The Bonds in Ethene -- CHEMICAL CONNECTION: Diamond, Graphite, Graphene, and Fullerenes: Substances that Contain Only Carbon Atoms -- 1.9 How a Triple Bond is Formed: The Bonds in Ethyne -- 1.10 The Bonds in the Methyl Cation, the Methyl Radical, and the Methyl Anion -- 1.11 The Bonds in Ammonia and in the Ammonium Ion -- 1.12 The Bonds in Water -- CHEMICAL CONNECTION: Water-A Unique Compound -- 1.13 The Bond in a Hydrogen Halide -- 1.14 Hybridization and Molecular Geometry -- PROBLEM-SOLVING STRATEGY -- 1.15 Summary: Hybridization, Bond Lengths, Bond Strengths, and Bond Angles -- PROBLEM-SOLVING STRATEGY -- 1.16 Dipole Moments of Molecules -- ESSENTIAL CONCEPTS -- PROBLEMS -- 2 Acids and Bases: Central to Understanding Organic Chemistry -- 2.1 An Introduction to Acids and Bases -- 2.2 pK[Sub(a)] and pH -- PROBLEM-SOLVING STRATEGY -- CHEMICAL CONNECTION: Acid Rain -- 2.3 Organic Acids and Bases -- BIOLOGICAL CONNECTION: Poisonous Amines -- PROBLEM-SOLVING STRATEGY -- 2.4 How to Predict the Outcome of an Acid-Base Reaction -- 2.5 How to Determine the Position of Equilibrium -- 2.6 How the Structure of an Acid Affects its pK[Sub(a)] Value -- 2.7 How Substituents Affect the Strength of an Acid.
PROBLEM-SOLVING STRATEGY -- 2.8 An Introduction to Delocalized Electrons -- PROBLEM-SOLVING STRATEGY -- MEDICAL CONNECTION: Fosamax Prevents Bones from Being Nibbled Away -- 2.9 A Summary of the Factors that Determine Acid Strength -- 2.10 How pH Affects the Structure of an Organic Compound -- PROBLEM-SOLVING STRATEGY -- CHEMICAL CONNECTION: Derivation of the Henderson-Hasselbalch Equation -- MEDICAL CONNECTION: Aspirin Must Be in its Basic Form to be Physiologically Active -- 2.11 Buffer Solutions -- MEDICAL CONNECTION: Blood: A Buffered Solution -- 2.12 Lewis Acids and Bases -- ESSENTIAL CONCEPTS -- PROBLEMS -- TUTORIAL Acids and Bases -- 3 An Introduction to Organic Compounds: Nomenclature, Physical Properties, and Structure -- 3.1 Alkyl Groups -- 3.2 The Nomenclature of Alkanes -- INDUSTRIAL CONNECTION: How is the Octane Number of Gasoline Determined? -- 3.3 The Nomenclature of Cycloalkanes -- PROBLEM-SOLVING STRATEGY -- 3.4 The Nomenclature of Alkyl Halides -- 3.5 The Nomenclature of Ethers -- 3.6 The Nomenclature of Alcohols -- 3.7 The Nomenclature of Amines -- CHEMICAL CONNECTION: Bad-Smelling Compounds -- 3.8 The Structures of Alkyl Halides, Alcohols, Ethers, and Amines -- 3.9 Noncovalent Interactions -- PROBLEM-SOLVING STRATEGY -- MEDICAL CONNECTION: Drugs Bind to Their Receptors -- 3.10 The Solubility of Organic Compounds -- BIOLOGICAL CONNECTION: Cell Membranes -- 3.11 Rotation Occurs about Carbon-Carbon Single Bonds -- 3.12 Some Cycloalkanes Have Angle Strain -- CHEMICAL CONNECTION: Von Baeyer, Barbituric Acid, and Blue Jeans -- PROBLEM-SOLVING STRATEGY -- 3.13 Conformers of Cyclohexane -- 3.14 Conformers of Monosubstituted Cyclohexanes -- CHEMICAL CONNECTION: Starch and Cellulose-Axial and Equatorial -- 3.15 Conformers of Disubstituted Cyclohexanes -- PROBLEM-SOLVING STRATEGY -- PROBLEM-SOLVING STRATEGY -- 3.16 Fused Cyclohexane Rings. MEDICAL CONNECTION: Cholesterol and Heart Disease -- MEDICAL CONNECTION: How High Cholesterol is Treated Clinically -- ESSENTIAL CONCEPTS -- PROBLEMS -- PART TWO: Electrophilic Addition Reactions, Stereochemistry, and Electron Delocalization -- TUTORIAL Using Molecular Models -- 4 Isomers: The Arrangement of Atoms in Space -- 4.1 Cis-Trans Isomers Result from Restricted Rotation -- CHEMICAL CONNECTION: Cis-Trans Interconversion in Vision -- 4.2 Using the E,Z System to Distinguish Isomers -- PROBLEM-SOLVING STRATEGY -- 4.3 A Chiral Object Has a Nonsuperimposable Mirror Image -- 4.4 An Asymmetric Center is a Cause of Chirality in a Molecule -- 4.5 Isomers with One Asymmetric Center -- 4.6 Asymmetric Centers and Stereocenters -- 4.7 How to Draw Enantiomers -- 4.8 Naming Enantiomers by the R,S System -- PROBLEM-SOLVING STRATEGY -- PROBLEM-SOLVING STRATEGY -- 4.9 Chiral Compounds Are Optically Active -- 4.10 How Specific Rotation Is Measured -- 4.11 Enantiomeric Excess -- 4.12 Compounds with More than One Asymmetric Center -- 4.13 Stereoisomers of Cyclic Compounds -- PROBLEM-SOLVING STRATEGY -- 4.14 Meso Compounds Have Asymmetric Centers but Are Optically Inactive -- PROBLEM-SOLVING STRATEGY -- 4.15 How to Name Isomers with More than One Asymmetric Center -- PROBLEM-SOLVING STRATEGY -- 4.16 Nitrogen and Phosphorus Atoms Can Be Asymmetric Centers -- 4.17 Receptors -- MEDICAL CONNECTION: The Enantiomers of Thalidomide -- 4.18 How Enantiomers Can Be Separated -- PHARMACEUTICAL CONNECTION: Chiral Drugs -- ESSENTIAL CONCEPTS -- PROBLEMS -- TUTORIAL Interconverting Structural Representations -- 5 Alkenes: Structure, Nomenclature, and an Introduction to Reactivity Thermodynamics and Kinetics -- ENVIRONMENTAL CONNECTION: Pheromones -- 5.1 Molecular Formulas and the Degree of Unsaturation -- 5.2 The Nomenclature of Alkenes -- 5.3 The Structure of Alkenes. PROBLEM-SOLVING STRATEGY -- 5.4 How An Organic Compound Reacts Depends on Its Functional Group -- 5.5 How Alkenes React Curved Arrows Show the Flow of Electrons -- GENERAL CONNECTION: A Few Words About Curved Arrows -- 5.6 Thermodynamics: How Much Product is Formed? -- 5.7 Increasing the Amount of Product Formed in a Reaction -- 5.8 Calculating & -- #916 -- H° Values -- 5.9 Using & -- #916 -- H° Values to Determine the Relative Stabilities of Alkenes -- PROBLEM-SOLVING STRATEGY -- NUTRITIONAL CONNECTION: Trans Fats -- 5.10 Kinetics: How Fast is the Product Formed? -- 5.11 The Rate of a Chemical Reaction -- CHEMICAL CONNECTION: The Difference between 5.11 The Rate of a Chemical Reaction & -- #916 -- G[Sup(& -- #0135 -- )] and E[Sub(a)] -- 5.12 A Reaction Coordinate Diagram Describes the Energy Changes That Take Place During a Reaction -- 5.13 Catalysis -- 5.14 Catalysis by Enzymes -- ESSENTIAL CONCEPTS -- PROBLEMS -- CHEMICAL CONNECTION: Calculating Kinetic Parameters -- TUTORIAL Drawing Curved Arrows -- 6 The Reactions of Alkenes The Stereochemistry of Addition Reactions -- 6.1 The Addition of a Hydrogen Halide to an Alkene -- 6.2 Carbocation Stability Depends on the Number of Alkyl Groups Attached to the Positively Charged Carbon -- 6.3 What Does the Structure of the Transition State Look Like? -- 6.4 Electrophilic Addition Reactions Are Regioselective -- PROBLEM-SOLVING STRATEGY -- 6.5 The Addition of Water to an Alkene -- 6.6 The Addition of an Alcohol to an Alkene -- 6.7 A Carbocation Will Rearrange if It Can Form a More Stable Carbocation -- 6.8 The Addition of Borane to an Alkene: Hydroboration-Oxidation -- CHEMICAL CONNECTION: Borane and Diborane -- 6.9 The Addition of a Halogen to an Alkene -- PROBLEM-SOLVING STRATEGY -- 6.10 The Addition of a Peroxyacid to an Alkene -- 6.11 The Addition of Ozone to an Alkene: Ozonolysis. PROBLEM-SOLVING STRATEGY -- 6.12 Regioselective, Stereoselective, And Stereospecific Reactions -- 6.13 The Stereochemistry of Electrophilic Addition Reactions -- CHEMICAL CONNECTION: Cyclic Alkenes -- PROBLEM-SOLVING STRATEGY -- 6.14 The Stereochemistry of Enzyme-Catalyzed Reactions -- 6.15 Enantiomers Can Be Distinguished by Biological Molecules -- CHEMICAL CONNECTION: Chiral Catalysts -- 6.16 Reactions and Synthesis -- ENVIRONMENTAL CONNECTION: Which are More Harmful: Natural Pesticides or Synthetic Pesticides? -- ESSENTIAL CONCEPTS -- SUMMARY OF REACTIONS -- PROBLEMS -- 7 The Reactions of Alkynes An Introduction to Multistep Synthesis -- MEDICAL CONNECTION: Synthetic Alkynes Are Used to Treat Parkinson's Disease -- PHARMACEUTICAL CONNECTION: Why Are Drugs so Expensive? -- 7.1 The Nomenclature of Alkynes -- MEDICAL CONNECTION: Synthetic Alkynes Are Used for Birth Control -- 7.2 How to Name a Compound That Has More than One Functional Group -- 7.3 The Structure of Alkynes -- BIOLOGICAL CONNECTION: How a Banana Slug Knows What to Eat -- 7.4 The Physical Properties of Unsaturated Hydrocarbons -- 7.5 The Reactivity of Alkynes -- 7.6 The Addition of Hydrogen Halides and the Addition of Halogens to an Alkyne -- 7.7 The Addition of Water to an Alkyne -- 7.8 The Addition of Borane to an Alkyne: Hydroboration-Oxidation -- 7.9 The Addition of Hydrogen to an Alkyne -- 7.10 A Hydrogen Bonded to an sp Carbon Is "Acidic -- CHEMICAL CONNECTION: Sodium Amide and Sodium in Ammonia -- PROBLEM-SOLVING STRATEGY -- 7.11 Synthesis Using Acetylide Ions -- 7.12 DESIGNING A SYNTHESIS I: An Introduction to Multistep Synthesis -- ENVIRONMENTAL CONNECTION: Green Chemistry: Aiming for Sustainability -- ESSENTIAL CONCEPTS -- SUMMARY OF REACTIONS -- PROBLEMS. 8 Delocalized Electrons: Their Effect on Stability, pK[Sub(a)] , and the Products of a Reaction Aromaticity and Electronic Effects: An Introduction to the Reactions of Benzene. |
| Record Nr. | UNINA-9910154959303321 |
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Bruice Paula Yurkanis <1941->
|
||
| Harlow, England : , : Pearson, , [2017] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Study guide and student's solutions manual for organic chemistry / / Paula Y. Bruice
| Study guide and student's solutions manual for organic chemistry / / Paula Y. Bruice |
| Autore | Bruice Paula Yurkanis <1941-> |
| Edizione | [Seventh, Pearson new international edition.] |
| Pubbl/distr/stampa | Harlow, England : , : Pearson, , [2014] |
| Descrizione fisica | 1 online resource (899 pages) : illustrations |
| Disciplina | 547.0076 |
| Collana | Always Learning |
| Soggetto topico | Chemistry, Organic |
| ISBN |
1-292-05217-1
9781292052175 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover -- Table of Contents -- 1. Spectroscopy Problems -- 2. Remembering General Chemistry: Electronic Structure and Bonding -- 3. Acids and Bases: Central to Understanding Organic Chemistry -- 4. SPECIAL TOPIC I: pH, pKa, and Buffers -- 5. An Introduction to Organic Compounds: Nomenclature, Physical Properties, and Representation of Structure -- 6. Isomers: The Arrangement of Atoms in Space -- 7. Alkenes: Structure, Nomenclature, and an Introduction to Reactivity Thermodynamics and Kinetics -- 8. The Reactions of Alkenes: The Stereochemistry of Addition Reactions -- 9. The Reactions of Alkynes An Introduction to Multistep Synthesis -- 10. Delocalized Electrons and Their Effect on Stability, pKa, and the Products of a Reaction -- 11. SPECIAL TOPIC II: Molecular Orbital Theory -- 12. Substitution Reactions of Alkyl Halides -- 13. Elimination Reactions of Alkyl Halides Competition Between Substitution and Elimination -- 14. Reactions of Alcohols, Ethers, Epoxides, Amines, and Thiols -- 15. Organometallic Compounds -- 16. Radicals Reactions of Alkanes -- 17. NMR Spectroscopy -- 18. Mass Spectrometry, Infrared Spectroscopy, and Ultraviolet/Visible Spectroscopy -- 19. Reactions of Carboxylic Acids and Carboxylic Acid Derivatives -- 20. Reactions of Aldehydes and Ketones More Reactions of Carboxylic Acid Derivatives Reactions of α, β-Unsaturated Carbonyl Compounds -- 21. Reactions at the α-Carbon of Carbonyl Compounds -- 22. Reactions of Benzene and Substituted Benzenes -- 23. More About Amines Reactions of Heterocyclic Compounds -- 24. The Organic Chemistry of Carbohydrates -- 25. The Organic Chemistry of Amino Acids, Peptides, and Proteins -- 26. Catalysis in Organic Reactions and in Enzymatic Reactions -- 27. The Organic Chemistry of the Coenzymes, Compounds Derived from Vitamins.
28. The Organic Chemistry of the Metabolic Pathways Terpene Biosynthesis -- 29. The Chemistry of the Nucleic Acids -- 30. Synthetic Polymers -- 31. Pericyclic Reactions -- Index. |
| Record Nr. | UNINA-9910153080503321 |
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Bruice Paula Yurkanis <1941->
|
||
| Harlow, England : , : Pearson, , [2014] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||