000			10122cam a2200553Ii 4500
001			ocn903531524
003			OCoLC
005			20190328114810.0
006			m o d
007			cr cnu|||unuuu
008			150217t20152015ne a o 001 0 eng d
040			_aN$T _beng _erda _epn _cN$T _dEBLCP _dN$T _dOPELS _dTEFOD _dE7B _dOCLCF _dCHVBK _dDEBSZ _dOCL _dYDXCP _dTEFOD _dIDEBK _dFEM _dS4S _dOCLCQ _dBUF _dUUM _dU3W _dD6H _dNLE _dUKMGB _dOCLCQ _dOCLCO _dWYU _dG3B _dS9I _dJF0
016	7		_a017859510 _2Uk
019			_a968013095 _a969026898 _a1066451702
020			_a9780128026342 _q(electronic bk.)
020			_a0128026340 _q(electronic bk.)
020			_z9780128024447
035			_a(OCoLC)903531524 _z(OCoLC)968013095 _z(OCoLC)969026898 _z(OCoLC)1066451702
050		4	_aQD251.3
072		7	_aSCI _x013040 _2bisacsh
082	0	4	_a547
100	1		_aOuellette, Robert J., _d1938- _eauthor.
245	1	0	_aPrinciples of organic chemistry / _h[electronic resource] _cRobert J. Ouellette, J. David Rawn.
264		1	_aAmsterdam : _bElsevier, _c[2015]
264		4	_c�2015
300			_a1 online resource : _billustrations
336			_atext _btxt _2rdacontent
337			_acomputer _bc _2rdamedia
338			_aonline resource _bcr _2rdacarrier
347			_atext file _2rda
588	0		_aOnline resource; title from PDF title page (EBSCO, viewed February 23, 2015).
500			_aIncludes index.
520			_aClass-tested and thoughtfully designed for student engagement, Principles of Organic Chemistry provides the tools and foundations needed by students in a short course or one-semester class on the subject. This book does not dilute the material or rely on rote memorization. Rather, it focuses on the underlying principles in order to make accessible the science that underpins so much of our day-to-day lives, as well as present further study and practice in medical and scientific fields. This book provides context and structure for learning the fundamental principles of organic chemistry, enabling the reader to proceed from simple to complex examples in a systematic and logical way. Utilizing clear and consistently colored figures, Principles of Organic Chemistry begins by exploring the step-by-step processes (or mechanisms) by which reactions occur to create molecular structures. It then describes some of the many ways these reactions make new compounds, examined by functional groups and corresponding common reaction mechanisms. Throughout, this book includes biochemical and pharmaceutical examples with varying degrees of difficulty, with worked answers and without, as well as advanced topics in later chapters for optional coverage.
505	0		_aFront Cover -- Principles of Organic Chemistry -- Copyright -- Table of Contents -- Chapter 1: Structure of Organic Compounds -- 1.1 Organic and Inorganic Compounds -- 1.2 Atomic Structure -- 1.3 Types of Bonds -- 1.4 Formal Charge -- 1.5 Resonance Structures -- 1.6 Predicting the Shapes of Simple Molecules -- 1.7 Orbitals and Molecular Shapes -- 1.8 Functional Groups -- 1.9 Structural Formulas -- 1.10 Isomers -- 1.11 Nomenclature -- Exercises -- Chapter 2: Properties of Organic Compounds -- 2.1 Structure and Physical Properties -- 2.2 Chemical Reactions -- 2.3 Acid-Base Reactions -- 2.4 Oxidation-Reduction Reactions -- 2.5 Classification of Organic Reactions -- 2.6 Chemical Equilibrium and Equilibrium Constants -- 2.7 Equilibria in Acid-Base Reactions -- 2.8 Effect of Structure on Acidity -- 2.9 Introduction to Reaction Mechanisms -- 2.10 Reaction Rates -- Exercises -- Chapter 3: Alkanes and Cycloalkanes -- 3.1 Classes of Hydrocarbons -- 3.2 Alkanes -- 3.3 Nomenclature of Alkanes -- 3.4 Conformations of Alkanes -- 3.5 Cycloalkanes -- 3.6 Conformations of Cycloalkanes -- 3.7 Physical Properties of Alkanes -- 3.8 Oxidation of Alkanes and Cycloalkanes -- 3.9 Halogenation of Saturated Alkanes -- 3.10 Nomenclature of Haloalkanes -- Summary of Reactions -- Exercises -- Chapter 4: Alkenes and Alkynes -- 4.1 Unsaturated Hydrocarbons -- 4.2 Geometric Isomerism -- 4.3 E, Z Nomenclature of Geometrical Isomers -- 4.4 Nomenclature of Alkenes and Alkynes -- 4.5 Acidity of Alkenes and Alkynes -- 4.6 Hydrogenation of Alkenes and Alkynes -- 4.7 Oxidation of Alkenes and Alkynes -- 4.8 Addition Reactions of Alkenes and Alkynes -- 4.9 Mechanism of Addition Reactions -- 4.10 Hydration of Alkenes and Alkynes.
505	8		_a4.11 Preparation of Alkenes and Alkynes -- 4.12 Alkadienes (Dienes) -- 4.13 Terpenes -- Summary of Reactions -- Exercises -- Chapter 5: Aromatic Compounds -- 5.1 Aromatic Compounds -- 5.2 Aromaticity -- 5.3 Nomenclature of Aromatic Compounds -- 5.4 Electrophilic Aromatic Substitution -- 5.5 Structural Effects in Electrophilic Aromatic Substitution -- 5.6 Interpretation of Rate Effects -- 5.7 Interpretation of Directing Effects -- 5.8 Reactions of Side Chains -- 5.9 Functional Group Modification -- 5.10 Synthesis of Substituted Aromatic Compounds -- Summary of Reactions -- Exercises -- Chapter 6: Stereochemistry -- 6.1 Configuration of Molecules -- 6.2 Mirror Images and Chirality -- 6.3 Optical Activity -- 6.4 Fischer Projection Formulas -- 6.5 Absolute Configuration -- 6.6 Molecules with Multiple Stereogenic Centers -- 6.7 Synthesis of Stereoisomers -- 6.8 Reactions that Produce Stereogenic Centers -- 6.9 Reactions that Form Diastereomers -- Exercises -- Chapter 7: Nucleophilic Substitution and Elimination Reactions -- 7.1 Reaction Mechanisms and Haloalkanes -- 7.2 Nucleophilic Substitution Reactions -- 7.3 Nucleophilicity Versus Basicity -- 7.4 Mechanisms of Substitution Reactions -- 7.5 SN2 Versus SN1 Reactions -- 7.6 Mechanisms of Elimination Reactions -- 7.7 Effect of Structure on Competing Reactions -- Summary of Reactions -- Exercises -- Chapter 8: Alcohols and Phenols -- 8.1 The Hydroxyl Group -- 8.2 Physical Properties of Alcohols -- 8.3 Acid-Base Reactions of Alcohols -- 8.4 Substitution Reactions of Alcohols -- 8.5 Dehydration of Alcohols -- 8.6 Oxidation of Alcohols -- 8.7 Synthesis of Alcohols -- 8.8 Phenols -- 8.9 Sulfur Compounds: Thiols and Thioethers -- Summary of Reactions -- Exercises -- Chapter 9: Ethers and Epoxides -- 9.1 Structure of Ethers.
505	8		_a9.2 Nomenclature of Ethers -- 9.3 Physical Properties of Ethers -- 9.4 The Grignard Reagent and Ethers -- 9.5 Synthesis of Ethers -- 9.6 Reactions of Ethers -- 9.7 Synthesis of Epoxides -- 9.8 Reactions of Epoxides -- Summary of Reactions -- Exercises -- Chapter 10: Aldehydes and Ketones -- 10.1 The Carbonyl Group -- 10.2 Nomenclature of Aldehydes and Ketones -- 10.3 Physical Properties of Aldehydes and Ketones -- 10.4 Oxidation-Reduction Reactions of Carbonyl Compounds -- 10.5 Addition Reactions of Carbonyl Compounds -- 10.6 Synthesis of Alcohols from Carbonyl Compounds -- 10.7 Addition Reactions of Oxygen Compounds -- 10.8 Formation of Acetals and Ketals -- 10.9 Addition of Nitrogen Compounds -- 10.10 Reactivity of the Q-Carbon Atom -- 10.11 The Aldol Condensation -- Summary of Reactions -- Exercises -- Chapter 11: Carboxylic Acids and Esters -- 11.1 Carboxylic Acids and Acyl Groups -- 11.2 Nomenclature of Carboxylic Acids -- 11.3 Physical Properties of Carboxylic Acids -- 11.4 Acidity of Carboxylic Acids -- 11.5 Synthesis of Carboxylic Acids -- 11.6 Nucleophilic Acyl Substitution -- 11.7 Reduction of Acyl Derivatives -- 11.8 Esters and Anhydrides of Phosphoric Acid -- 11.9 The Claisen Condensation -- Summary of Reactions -- Exercises -- Chapter 12: Amines and Amides -- 12.1 Organic Nitrogen Compounds -- 12.2 Bonding and Structure of Amines -- 12.3 Structure and Classification of Amines and Amides -- 12.4 Nomenclature of Amines and Amides -- 12.5 Physical Properties of Amines -- 12.6 Basicity of Nitrogen Compounds -- 12.7 Solubility of Ammonium Salts -- 12.8 Nucleophilic Reactions of Amines -- 12.9 Synthesis of Amines -- 12.10 Hydrolysis of Amides -- 12.11 Synthesis of Amides -- Summary of Reactions -- Exercises -- Chapter 13: Carbohydrates.
505	8		_a13.1 Classification of Carbohydrates -- 13.2 Chirality of Carbohydrates -- 13.3 Hemiacetals and Hemiketals -- 13.4 Conformations of Monosaccharides -- 13.5 Reduction of Monosaccharides -- 13.6 Oxidation of Monosaccharides -- 13.7 Glycosides -- 13.8 Disaccharides -- 13.9 Polysaccharides -- Summary of Reactions -- Exercises -- Chapter 14: Amino Acids, Peptides, and Proteins -- 14.1 Proteins Andpolypeptides -- 14.2 Amino Acids -- 14.3 Acid-Base Properties of Q-Amino Acids -- 14.4 Isoionic Point -- 14.5 Peptides -- 14.6 Peptide Synthesis -- 14.7 Determination of Protein Structure -- 14.8 Protein Structure -- Exercises -- Chapter 15: Synthetic Polymers -- 15.1 Natural and Synthetic Macromolecules -- 15.2 Structure and Properties of Polymers -- 15.3 Classification of Polymers -- 15.4 Methods of Polymerization -- 15.5 Addition Polymerization -- 15.6 Copolymerization of Alkenes -- 15.7 Cross-Linked Polymers -- 15.8 Stereochemistry of Addition Polymerization -- 15.9 Condensation Polymers -- 15.10 Polyesters -- 15.11 Polycarbonates -- 15.12 Polyamides -- 15.13 Polyurethanes -- Exercises -- Chapter 16: Spectroscopy -- 16.1 Spectroscopic Structure Determination -- 16.2 Spectroscopic Principles -- 16.3 Ultraviolet Spectroscopy -- 16.4 Infrared Spectroscopy -- 16.5 Nuclear Magnetic Resonance Spectroscopy -- 16.6 Spin-Spin Splitting -- 16.7 13C NMR Spectroscopy -- Exercises -- Solutions to In-Chapter Problems -- Index -- Back Cover.
650		0	_aChemistry, Organic.
650		0	_aChemistry, Organic _vProblems, exercises, etc.
650		7	_aSCIENCE _xChemistry _xOrganic. _2bisacsh
650		7	_aChemistry, Organic. _2fast _0(OCoLC)fst00853501
650		7	_aOrganische Chemie _2gnd _0(DE-588)4043793-0
655		7	_aProblems and exercises. _2fast _0(OCoLC)fst01423783
655		4	_aElectronic books.
655		0	_aElectronic books.
700	1		_aRawn, J. David, _d1944- _eauthor.
776	0	8	_iPrint version: _aOuellette, Robert J. _tPrinciples of Organic Chemistry. _dSaint Louis : Elsevier Science, �2015 _z9780128024447
856	4	0	_3ScienceDirect _uhttp://www.sciencedirect.com/science/book/9780128024447
999			_c247047 _d247047