Principles of organic chemistry / (Record no. 247047)
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| control field | ocn903531524 |
| 003 - CONTROL NUMBER IDENTIFIER | |
| control field | OCoLC |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20190328114810.0 |
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| 007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION | |
| fixed length control field | cr cnu|||unuuu |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 150217t20152015ne a o 001 0 eng d |
| 040 ## - CATALOGING SOURCE | |
| Original cataloging agency | N$T |
| Language of cataloging | eng |
| Description conventions | rda |
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| Transcribing agency | N$T |
| Modifying agency | EBLCP |
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| 016 7# - NATIONAL BIBLIOGRAPHIC AGENCY CONTROL NUMBER | |
| Record control number | 017859510 |
| Source | Uk |
| 019 ## - | |
| -- | 968013095 |
| -- | 969026898 |
| -- | 1066451702 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 9780128026342 |
| Qualifying information | (electronic bk.) |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 0128026340 |
| Qualifying information | (electronic bk.) |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| Canceled/invalid ISBN | 9780128024447 |
| 035 ## - SYSTEM CONTROL NUMBER | |
| System control number | (OCoLC)903531524 |
| Canceled/invalid control number | (OCoLC)968013095 |
| -- | (OCoLC)969026898 |
| -- | (OCoLC)1066451702 |
| 050 #4 - LIBRARY OF CONGRESS CALL NUMBER | |
| Classification number | QD251.3 |
| 072 #7 - SUBJECT CATEGORY CODE | |
| Subject category code | SCI |
| Subject category code subdivision | 013040 |
| Source | bisacsh |
| 082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER | |
| Classification number | 547 |
| 100 1# - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Ouellette, Robert J., |
| Dates associated with a name | 1938- |
| Relator term | author. |
| 245 10 - TITLE STATEMENT | |
| Title | Principles of organic chemistry / |
| Medium | [electronic resource] |
| Statement of responsibility, etc. | Robert J. Ouellette, J. David Rawn. |
| 264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
| Place of production, publication, distribution, manufacture | Amsterdam : |
| Name of producer, publisher, distributor, manufacturer | Elsevier, |
| Date of production, publication, distribution, manufacture, or copyright notice | [2015] |
| 264 #4 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
| Date of production, publication, distribution, manufacture, or copyright notice | �2015 |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | 1 online resource : |
| Other physical details | illustrations |
| 336 ## - CONTENT TYPE | |
| Content type term | text |
| Content type code | txt |
| Source | rdacontent |
| 337 ## - MEDIA TYPE | |
| Media type term | computer |
| Media type code | c |
| Source | rdamedia |
| 338 ## - CARRIER TYPE | |
| Carrier type term | online resource |
| Carrier type code | cr |
| Source | rdacarrier |
| 347 ## - DIGITAL FILE CHARACTERISTICS | |
| File type | text file |
| Source | rda |
| 588 0# - SOURCE OF DESCRIPTION NOTE | |
| Source of description note | Online resource; title from PDF title page (EBSCO, viewed February 23, 2015). |
| 500 ## - GENERAL NOTE | |
| General note | Includes index. |
| 520 ## - SUMMARY, ETC. | |
| Summary, etc. | Class-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# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | Front 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# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | 4.11 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# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | 9.2 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# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | 13.1 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 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | Chemistry, Organic. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | Chemistry, Organic |
| Form subdivision | Problems, exercises, etc. |
| 650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | SCIENCE |
| General subdivision | Chemistry |
| -- | Organic. |
| Source of heading or term | bisacsh |
| 650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | Chemistry, Organic. |
| Source of heading or term | fast |
| Authority record control number | (OCoLC)fst00853501 |
| 650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | Organische Chemie |
| Source of heading or term | gnd |
| Authority record control number | (DE-588)4043793-0 |
| 655 #7 - INDEX TERM--GENRE/FORM | |
| Genre/form data or focus term | Problems and exercises. |
| Source of term | fast |
| Authority record control number | (OCoLC)fst01423783 |
| 655 #4 - INDEX TERM--GENRE/FORM | |
| Genre/form data or focus term | Electronic books. |
| 655 #0 - INDEX TERM--GENRE/FORM | |
| Genre/form data or focus term | Electronic books. |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Rawn, J. David, |
| Dates associated with a name | 1944- |
| Relator term | author. |
| 776 08 - ADDITIONAL PHYSICAL FORM ENTRY | |
| Relationship information | Print version: |
| Main entry heading | Ouellette, Robert J. |
| Title | Principles of Organic Chemistry. |
| Place, publisher, and date of publication | Saint Louis : Elsevier Science, �2015 |
| International Standard Book Number | 9780128024447 |
| 856 40 - ELECTRONIC LOCATION AND ACCESS | |
| Materials specified | ScienceDirect |
| Uniform Resource Identifier | http://www.sciencedirect.com/science/book/9780128024447 |
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