Designed specifically for the one-semester short course in organic chemistry, this market leader appeals to a range of non-chemistry science majors through its emphasis on practical, real-life applications of chemistry, coverage of basic concepts, and engaging visual style. In contrast to competitors who offer mainly streamlined versions of full-year texts, this text has always been aimed at the short course and its writing style, approach, and selection of topics best suit the needs of this market. The Twelfth Edition further develops the strengths of the previous editions through an updated, dynamic art program--online, on CD, and in the text--new content to keep students current with developments in the organic chemistry field, and a revised lab manual.
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Descrizione libro Brooks Cole, 2006. Hardcover. Condizione libro: New. 12. Codice libro della libreria DADAX0618590730
Descrizione libro Cengage Learning, 2006. Condizione libro: New. Brand New, Unread Copy in Perfect Condition. A+ Customer Service! Summary: Preliminary Contents Note: Each chapter concludes with Additional Problems. 1. Bonding and Isomerism 1.1 How Electrons are Arranged in Atoms 1.2 Ionic and Covalent Bonding 1.3 Carbon and the Covalent Bond 1.4 Carbon-Carbon Single Bonds 1.5 Polar Covalent Bonds 1.6 Multiple Covalent Bonds 1.7 Valence 1.8 Isomerism 1.9 Writing Structural Formulas 1.10 Abbreviated Structural Formulas 1.11 Formal Charge 1.12 Resonance 1.13 Arrow Formalism 1.14 The Orbital View of Bonding; the Sigma Bond 1.15 Carbon sp3 Hybrid Orbitals 1.16 Tetrahedral Carbon; the Bonding in Methane 1.17 Classification According to Molecular Framework 1.18 Classification According to Functional Group 2. Alkanes and Cycloalkanes: Conformational and Geometric Isomerism 2.1 The Structures of Alkanes 2.2 Nomenclature of Organic Compounds 2.3 IUPAC Rules for Naming Alkanes 2.4 Alkyl and Halogen Substituents 2.5 Use of the IUPAC Rules 2.6 Sources of Alkanes A Closer Look At.Natural Gas 2.7 Physical Properties of Alkanes and Nonbonding Intermolecular Interactions A Closer Look At.Hydrogen Bonding 2.8 Conformations of Alkanes 2.9 Cycloalkane Nomenclature and Conformation 2.10 Cis-trans Isomerism in Cycloalkanes 2.11 Summary of Isomerism A Word About: Isomers, Possible and Impossible 2.12 Reactions of Alkanes A Word About: Methane, Marsh Gas, and Miller's Experiment 2.13 The Free-Radical Chain Mechanism of Halogenation Reaction Summary Mechanism Summary 3. Alkenes and Alkynes 3.1 Definition and Classification 3.2 Nomenclature 3.3 Some Facts About Double Bonds 3.4 The Orbital Model of a Double Bond; the Pi Bond 3.5 Cis-trans Isomerism in Alkenes A Word About: The Chemistry of Vision 3.6 Addition and Substitution Reactions Compared 3.7 Polar Addition Reactions 3.8 Addition of Unsymmetric Reagents to Unsymmetric Alkenes; Markovnikov's Rule 3.9 Mechanism of Electrophilic Addition to Alkenes 3.10 Markovnikov's Rule Explained 3.11 Reaction Equilibrium: What Makes a Reaction Go? 3.12 Reaction Rates: How Fast Does a Reaction Go? 3.13 Hydroboration of Alkenes 3.14 Addition of Hydrogen 3.15 Additions to Conjugated Systems 3.16 Free-Radical Addition 3.17 Oxidation of Alkenes A Word About: Ethylene: Raw Material and Plant Hormone 3.18 Some Facts About Triple Bonds 3.19 The Orbital Model of a Triple Bonds 3.20 Additon Reactions of Alkynes 3.21 Acidity of Alkynes A Word About: Petroleum, Gasoline, and Octane Number Reaction Summary Mechanism Summary 4. Aromatic Compounds 4.1 Some Facts About Benzene 4.2 The Kekuleacute; Structure of Benzene 4.3 The Resonance Model for Benzene 4.4 Orbital Model for Benzene 4.5 Symbols for Benzene 4.6 Nomenclature of Aromatic Compounds 4.7 The Resonance Energy of Benzene 4.8 Electrophilic Substitution 4.9 The Mechanism of Electrophilic Aromatic Substitution 4.10 Ring-Activating and Ring-Deactivating Substituents 4.11 Ortho, Para-Directing, and Meta-Directing Groups 4.12 The Importance of Directing Effects in Synthesis 4.13 Polycyclic Aromatic Hydrocarbons A Word About: Polycyclic Aromatic Hydrocarbons and Cancer A Word About: C60, an Aromatic Sphere: The Fullerenes Reaction Summary Mechanism Summary 5. Stereoisomerism 5.1 Chirality and Enantiomers 5.2 Stereogenic Centers; the Stereogenic Carbon Atom 5.3 Configuration and the R-S Convention 5.4 The E-Z Convention for Cis-trans Isomers 5.5 Polarized Light and Optical Activity A Word About: Pasteur's Experiments and the van't Hoff-LeBel Explanation 5.6 Properties of Enantiomers 5.7 Fischer Projection Formulas 5.8 Compounds with More Than One Stereogenic Center; Diastereomers 5.9 Meso Compounds; the Stereoisomers of Tartaric Acid 5.10 Stereochemistry; a Recap of Definitions 5.11 Stereochemistry and Chemical Reactions 5.12 Resolution of a Racemic Mixture A Word About: Enantiomers and Biological Activity 6. Organic Halogen Compounds; Substitution and Elimination Reactions 6.1 Nucleophilic Substitution 6.2 Examples of Nucleophilic Substitu. Codice libro della libreria ABE_book_new_0618590730
Descrizione libro Cengage Learning, 2006. Hardcover. Condizione libro: New. book. Codice libro della libreria 0618590730
Descrizione libro Brooks Cole, 2006. Hardcover. Condizione libro: New. Codice libro della libreria P110618590730
Descrizione libro Hardcover. Condizione libro: BRAND NEW. BRAND NEW. Fast Shipping. Prompt Customer Service. Satisfaction guaranteed. Codice libro della libreria 0618590730BNA