MARC details
| 000 -CABECERA |
|---|
| campo de control de longitud fija |
06630cam a22002414a 4500 |
| 008 - DATOS DE LONGITUD FIJA--INFORMACIÓN GENERAL |
|---|
| campo de control de longitud fija |
1977 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| International Standard Book Number |
0070414572 |
| 040 ## - FUENTE DE CATALOGACIÓN |
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| Centro catalogador/agencia de origen |
GAMADERO |
| Lengua de catalogación |
SPA |
| Centro/agencia transcriptor |
GAMADERO |
| 041 ## - CÓDIGO DE IDIOMA |
|---|
| Código de lengua del texto/banda sonora o título independiente |
Inglés |
| 050 00 - SIGNATURA TOPOGRÁFICA DE LA BIBLIOTECA DEL CONGRESO |
|---|
| Número de clasificación |
QD257 |
| Cutter |
MM4 |
| Año |
1977 |
| 100 ## - ENTRADA PRINCIPAL--NOMBRE DE PERSONA |
|---|
| Nombre de persona |
HERBERT MEISLICH |
| 9 (RLIN) |
3987 |
| 245 00 - MENCIÓN DEL TÍTULO |
|---|
| Título |
ORGANIC CHEMISTRY |
| 250 ## - MENCION DE EDICION |
|---|
| Mención de edición |
1er.edición |
| 260 3# - PUBLICACIÓN, DISTRIBUCIÓN, ETC. |
|---|
| Lugar de publicación, distribución, etc. |
Estados Unidos |
| Nombre del editor, distribuidor, etc. |
McGraw-Hill,Inc |
| Fecha de publicación, distribución, etc. |
1977 |
| 300 ## - DESCRIPCIÓN FÍSICA |
|---|
| Extensión |
480 pg |
| Otras características físicas |
Ilustrado |
| Dimensiones |
17 cm x 27 cm |
| 505 ## - NOTA DE CONTENIDO CON FORMATO |
|---|
| Nota de contenido con formato |
Chapter 1<br/>STRUCTURE AND PROPERTIES<br/>1.1 Organic Compounds<br/>Chapter 2<br/>BONDING AND MOLECULAR STRUCTURE<br/>Atomic Orbitals<br/>Covalent Bond Formation-Molecular Orbital (MO) Method<br/>Hybridization of Atomic Orbitals Electronegativity and Polarity<br/>Oxidation Number<br/>Intermolecular (vander Waals) Forces Resonance and Delocalized p Electrons<br/>Chapter 3 CHEMICAL REACTIVITY AND ORGANIC REACTIONS<br/>3.1 Reaction Mechanism<br/>3.2 Carbon-Containing Intermediates<br/>3.3 Types of Organic Reactions<br/>3.4 Electrophilic and Nucleophilic Reagents<br/>3.5 Thermodynamics<br/>3.6 Bond Dissociation Energies<br/>3.7 Chemical Equilibrium<br/>3.8 Rates of Reactions<br/>3.9 Transition-State Theory and Enthalpy Diagrams<br/>3.10 Acids and Bases<br/>Chapter 4 ALKANES<br/>4.1 Definition<br/>4.2 Nomenclature of Alkanes<br/>4.3 Preparation of Alkanes<br/>4.4 Chemical Properties of Alkanes<br/>Chapter 5<br/>STEREOCHEMISTRY<br/>5.1 Stereoisomerism<br/>5.2 Optical Isomerism<br/>5.3 Relative and Absolute Configuration<br/>5.4 Molecules with More than One Chiral Center<br/>5.5 Synthesis and Optical Activity<br/>Chapter 6 ALKENES<br/>6.1 Nomenclature and Structure<br/>6.2 Preparation of Alkenes<br/>6.3 Chemical Properties of Alkenes<br/>6.4 Electrophilic Polar Addition Reactions<br/>6.5 Summary of Alkene Chemistry<br/>Chapter 7<br/>ALKYL HALIDES<br/>7.1 Introduction<br/>7.2 Synthesis of R<br/>7.3 Chemical Properties<br/>7.4 Summary of Alkyl Halide Chemistry<br/>Chapter 8<br/>ALKYNES AND DIENES<br/>8.1 Alkynes<br/>8.2 Chemical Properties of Acetylenes<br/>8.3 Alkadienes<br/>8.4 Polymerization of Dienes<br/>8.5 Summary of Alkyne Chemistry<br/>8.6 Summary of Diene Chemistry<br/>Chapter 9<br/>ALICYCLIC COMPOUNDS<br/>9.1Nomenclature and Structure<br/>9.2Methods of Preparation<br/>9.3Conformations of Cycloalkanes<br/>Molecular-Orbital Interpretation of Concerted Cycloaddition<br/>Reactions: Woodward-Hoffmann Rules<br/>9.5 Terpenes and the Isoprene Rule<br/>Chapter 10 BENZENE AND AROMATICITY<br/>10.1 Introduction<br/>10.2 Aromaticity and Hückel's Rule<br/>10.3 Antiaromaticity<br/>10.4 Nomenclature<br/>Chapter 11 AROMATIC SUBSTITUTION. ARENES<br/>11.1 Aromatic Substitution by Electrophiles (Lewis Acids, E* or E)<br/>11.2 Nucleophilic and Free-Radical Substitutions<br/>11.3 Arenes<br/>Chapter 12 SPECTROSCOPY AND STRUCTURE<br/>12.1 Introduction<br/>12.2 Ultraviolet and Visible Spectroscopy<br/>12.3 Infrared Spectroscopy<br/>12.4 Nuclear Magnetic Resonance<br/>12.5 Mass Spectroscopy<br/>Chapter 13 ALCOHOLS<br/>13.1 General<br/>13.2 Preparation<br/>13.3 Reactions of Alcohols<br/>Chapter 14 ETHERS, EPOXIDES AND GLYCOLS<br/>14.1 Introduction and Nomenclature<br/>14.2 Preparation<br/>14.3 Chemical Properties<br/>14.4 Glycols<br/>14.5 Summary of Glycol Chemistry<br/>Chapter 15 THE CARBONYL COMPOUNDS<br/>15.1 Nomenclature<br/>15.2 Methods of Preparation<br/>15.3 Reactions of Aldehydes and Ketones<br/>Chapter 16 CARBOXYLIC ACIDS<br/>16.1 Introduction<br/>16.2 Preparation of Carboxylic Acids<br/>16.3 Reactions of Carboxylic Acids<br/>16.4 Summary of Carboxylic Acid Chemistry<br/>16.5 Analytical Detection of Carboxylic Acids<br/>Chapter 17 CARBOXYLIC ACID DERIVATIVES<br/>Chapter 18 AMINES<br/>18.1 Introduction and Nomenclature<br/>18.2 Preparation of Amines<br/>18.3 Chemical Properties of Amines<br/>18.4 Spectral Properties<br/>18.5 Reactions of Aryl Diazonium Salts<br/>17.1 Introduction<br/>17.2 Chemistry of Acyl Derivatives<br/>17.3 Dicarboxylic Acid Derivatives<br/>17.4 Claisen Condensation; Reactions of B-Ketoesters<br/>17.5 Lactones, Lactams<br/>17.6 Carbonic Acid Derivatives<br/>Chapter 19 ARYL HALIDES<br/>19.1 Introduction<br/>19.2 Reactions of Aryl Halides<br/>19.3 Methods of Preparation of Aryl Halides<br/>19.4 Chemical Properties<br/>Chapter 20 AROMATIC SULFONIC ACIDS;<br/>ORGANOSULFUR COMPOUNDS<br/>20.1 Introduction<br/>20.2 Preparation<br/>20.3 Chemical Properties<br/>20.4 Derivatives of Aromatic Sulfonic Acids<br/>20.5 Comparison of Sulfonic and Carborvlic Acid Chemistry<br/>20.6 Summary of Aliphatic Sulfur Compounds<br/>Chapter 21 PHENOLS<br/>21.1 Introduction<br/>21.2 Preparation<br/>21.3 Chemical Properties<br/>21.4 Analytical Detection of Phenols<br/>21.5 Summary of Phenols<br/>21.6 Summary of Ethers and Esters of Phenols<br/>Chapter 22 POLYNUCLEAR AROMATIC HYDROCARBONS<br/>22.1 Introduction<br/>22.2 Isolated Ring Systems<br/>22.3 Naphthalene<br/>22.4 Summary of Naphthalene Reactions<br/>Chapter 23 HETEROCYCLIC COMPOUNDS<br/>23.1 Introduction and Nomenclature<br/>23.2 Five-Membered Aromatic Heterocyclic Compounds. Furan (with O),<br/>Thiophene (with S), Pyrrole (with N)<br/>23.3 Six-Membered Heterocyclic Compounds<br/>23.4 Condensed Ring Systems<br/>Chapter 24 AMINO ACIDS AND PROTEINS<br/>24.1 Introduction<br/>24.2 Preparation of a-Amino Acids<br/>24.3 Acid-Base (Amphoteric) Properties<br/>24.4 Peptides<br/>24.5 Proteins<br/>Chapter 25 CARBOHYDRATES<br/>25.1 Introduction<br/>25.2 Chemical Properties of Monosaccharides<br/>25.3 Evidence for Hemiacetal Formation as Exemplified with Glucose<br/>25.4 Stereochemistry of Glucose<br/>25.5 Disaccharides<br/>25.6 Polysaccharides<br/>Chapter 26 CHEMICAL CALCULATIONS<br/>26.1 Formulas and Molecular Weights<br/>26.2 Colligative Properties<br/>26.3 Yields<br/>26.4 Neutralization Equivalent (NE)<br/>26.5 Chemical Equilibrium<br/>26.6 Distillation Problems<br/>26.7 Solvent Extraction |
| 520 ## - RESUMEN, ETC. |
|---|
| Resumen, etc. |
The beginning student in Organic Chemistry is often overwhelmed by facts, concepts, and new language. Each year, textbooks of Organic Chemistry grow in quantity of subject matter and in level of sophistication. This Schaum'S Outline was undertaken (initially by the senior author, . S.) to give a clear view of first-year Organic Chemistry through the solution of illustrative problems.<br/>Completely worked-out problems make up over 80% of the book, the remainder being a concise presentation of theory. The reader learns by thinking and doing rather than by being told.<br/>This outline can be used in support of a standard text, as a text to supplement a good set of lecture notes, as a review book for taking professional examinations, and as a vehicle for self-instruction.<br/>Our thanks and appreciation to Mr. Larry Alemany for his expert criticism from a student's viewpoint and for his careful proofreading, to Mr. David<br/>Beckwith for his editorial assistance, and to Mrs. Joyce Gaiser for her meticulous typing. |
| 526 ## - NOTA DE INFORMACIÓN SOBRE EL PROGRAMA DE ESTUDIO |
|---|
| Program name |
Ingenieria en Gestion Empresarial |
| 650 #0 - PUNTO DE ACCESO ADICIONAL DE MATERIA--TÉRMINO DE MATERIA |
|---|
| Término de materia o nombre geográfico como elemento de entrada |
Química |
| 9 (RLIN) |
48 |
| 700 ## - ENTRADA AGREGADA--NOMBRE PERSONAL |
|---|
| Nombre de persona |
HOWARD NECHAMKIN |
| 9 (RLIN) |
3989 |
| 942 ## - ELEMENTOS DE ENTRADA SECUNDARIOS (KOHA) |
|---|
| Fuente del sistema de clasificación o colocación |
Clasificación Decimal Dewey |
| Tipo de ítem Koha |
Libro |
| Edición |
1er.edición |
| Suprimir en OPAC |
No |
| 945 ## - CATALOGADORES |
|---|
| Número del Creador del Registro |
1260 |
| Nombre del Creador del Registro |
Norma Gabriela Corona Arreguin |
| Número de último modificador del registro |
1260 |
| Nombre del último modificador del registro |
Norma Gabriela Corona Arreguin |
