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Basic organic chemistry for the life sciences / / Hrvoj Vancik
| Basic organic chemistry for the life sciences / / Hrvoj Vancik |
| Autore | Vančik Hrvoj |
| Edizione | [Second edition.] |
| Pubbl/distr/stampa | Cham, Switzerland : , : Springer, , [2022] |
| Descrizione fisica | 1 online resource (213 pages) |
| Disciplina | 547 |
| Soggetto topico |
Chemistry, Organic
Química orgànica |
| Soggetto genere / forma | Llibres electrònics |
| ISBN |
9783030924386
9783030924379 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910523799303321 |
Vančik Hrvoj
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| Cham, Switzerland : , : Springer, , [2022] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Beilstein journal of organic chemistry
| Beilstein journal of organic chemistry |
| Pubbl/distr/stampa | [Frankfurt, Germany], : Beilstein-Institut |
| Descrizione fisica | 1 online resource |
| Soggetto topico |
Chemistry, Organic
Química orgànica |
| Soggetto genere / forma |
Periodical
Fulltext Internet Resources. Periodicals. Revistes electròniques. |
| Soggetto non controllato | Organic Chemistry |
| ISSN | 1860-5397 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | BJOC |
| Record Nr. | UNISA-996215494103316 |
| [Frankfurt, Germany], : Beilstein-Institut | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
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Beilstein journal of organic chemistry
| Beilstein journal of organic chemistry |
| Pubbl/distr/stampa | [Frankfurt, Germany], : Beilstein-Institut |
| Descrizione fisica | 1 online resource |
| Soggetto topico |
Chemistry, Organic
Química orgànica |
| Soggetto genere / forma |
Periodical
Fulltext Internet Resources. Periodicals. Revistes electròniques. |
| Soggetto non controllato | Organic Chemistry |
| ISSN | 1860-5397 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | BJOC |
| Record Nr. | UNINA-9910146207603321 |
| [Frankfurt, Germany], : Beilstein-Institut | ||
| 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->
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| Harlow, England : , : Pearson, , [2017] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Spectroscopic Methods in Organic Chemistry / / by Ian Fleming, Dudley Williams
| Spectroscopic Methods in Organic Chemistry / / by Ian Fleming, Dudley Williams |
| Autore | Fleming Ian <1935-> |
| Edizione | [7th ed. 2019.] |
| Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2019 |
| Descrizione fisica | 1 online resource (XI, 432 p. 466 illus., 16 illus. in color.) |
| Disciplina | 547.30858 |
| Soggetto topico |
Química orgànica
Espectroscòpia Spectroscopy Mass spectrometry Microscopy Organic chemistry Spectroscopy/Spectrometry Mass Spectrometry Spectroscopy and Microscopy Organic Chemistry |
| Soggetto genere / forma | Llibres electrònics |
| ISBN | 3-030-18252-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Chapter 1:Mass Spectra -- Chapter 2: Ultraviolet and visible spectra -- Chapter 3: Infrared spectra -- Chapter 4: 1D-NMR spectra -- Chapter 5: 2D-NMR spectra -- Chapter 6: Worked examples in structure determination -- Chapter 7: Problem sets -- Index. |
| Record Nr. | UNINA-9910370253703321 |
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Fleming Ian <1935->
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| Cham : , : Springer International Publishing : , : Imprint : Springer, , 2019 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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