Organic chemistry as a second language : (Record no. 34625)

MARC details
000 -LEADER
fixed length control field 06100cam a2200361 i 4500
001 - CONTROL NUMBER
control field 18961548
003 - CONTROL NUMBER IDENTIFIER
control field TH-BaNU
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20240402172004.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 201020s2016 nju 001 0 eng
010 ## - LIBRARY OF CONGRESS CONTROL NUMBER
LC control number 2016003041
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9781119110668 (pbk.)
040 ## - CATALOGING SOURCE
Original cataloging agency DLC
Language of cataloging eng
Transcribing agency DLC
Description conventions rda
Modifying agency DLC
-- TH-BaNU
042 ## - AUTHENTICATION CODE
Authentication code pcc
050 00 - LIBRARY OF CONGRESS CALL NUMBER
Classification number QD256
Item number K54145 2016
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Klein, David R.,
Dates associated with a name 1972-
Relator term author.
245 10 - TITLE STATEMENT
Title Organic chemistry as a second language :
Remainder of title first semester topics /
Statement of responsibility, etc. David Klein, Johns Hopkins University.
250 ## - EDITION STATEMENT
Edition statement 4e [é́dition].
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture Hoboken :
Name of producer, publisher, distributor, manufacturer Wiley,
Date of production, publication, distribution, manufacture, or copyright notice [2016]
300 ## - PHYSICAL DESCRIPTION
Extent xii, 382 pages :
Other physical details illustrations ;
Dimensions 24 cm
336 ## - CONTENT TYPE
Content type term text
Source rdacontent
337 ## - MEDIA TYPE
Media type term unmediated
Source rdamedia
338 ## - CARRIER TYPE
Carrier type term volume
Source rdacarrier
500 ## - GENERAL NOTE
General note Includes index.
505 ## - FORMATTED CONTENTS NOTE
Formatted contents note CHAPTER 1 BOND-LINE DRAWINGS 1<br/><br/>1.1 How to Read Bond-Line Drawings 1<br/><br/>1.2 How to Draw Bond-Line Drawings 5<br/><br/>1.3 Mistakes to Avoid 7<br/><br/>1.4 More Exercises 7<br/><br/>1.5 Identifying Formal Charges 9<br/><br/>1.6 Finding Lone Pairs that are Not Drawn 13<br/><br/>CHAPTER 2 RESONANCE 18<br/><br/>2.1 What is Resonance? 18<br/><br/>2.2 Curved Arrows: The Tools for Drawing Resonance Structures 19<br/><br/>2.3 The Two Commandments 21<br/><br/>2.4 Drawing Good Arrows 24<br/><br/>2.5 Formal Charges in Resonance Structures 26<br/><br/>2.6 Drawing Resonance Structures—Step by Step 30<br/><br/>2.7 Drawing Resonance Structures—by Recognizing Patterns 34<br/><br/>2.8 Assessing the Relative Importance of Resonance Structures 43<br/><br/>CHAPTER 3 ACID–BASE REACTIONS 49<br/><br/>3.1 Factor 1—What Atom is the Charge On? 50<br/><br/>3.2 Factor 2—Resonance 53<br/><br/>3.3 Factor 3—Induction 56<br/><br/>3.4 Factor 4—Orbitals 59<br/><br/>3.5 Ranking the Four Factors 60<br/><br/>3.6 Other Factors 63<br/><br/>3.7 Quantitative Measurement (pKa Values) 64<br/><br/>3.8 Predicting the Position of Equilibrium 65<br/><br/>3.9 Showing a Mechanism 66<br/><br/>CHAPTER 4 GEOMETRY 69<br/><br/>4.1 Orbitals and Hybridization States 69<br/><br/>4.2 Geometry 72<br/><br/>4.3 Lone Pairs 76<br/><br/>CHAPTER 5 NOMENCLATURE 77<br/><br/>5.1 Functional Group 78<br/><br/>5.2 Unsaturation 80<br/><br/>5.3 Naming the Parent Chain 81<br/><br/>5.4 Naming Substituents 84<br/><br/>5.5 Stereoisomerism 88<br/><br/>5.6 Numbering 90<br/><br/>5.7 Common Names 95<br/><br/>5.8 Going from a Name to a Structure 96<br/><br/>CHAPTER 6 CONFORMATIONS 97<br/><br/>6.1 How to Draw a Newman Projection 98<br/><br/>6.2 Ranking the Stability of Newman Projections 102<br/><br/>6.3 Drawing Chair Conformations 105<br/><br/>6.4 Placing Groups On the Chair 108<br/><br/>6.5 Ring Flipping 112<br/><br/>6.6 Comparing the Stability of Chairs 119<br/><br/>6.7 Don’t Be Confused by the Nomenclature 122<br/><br/>CHAPTER 7 CONFIGURATIONS 123<br/><br/>7.1 Locating Stereocenters 123<br/><br/>7.2 Determining the Configuration of a Stereocenter 126<br/><br/>7.3 Nomenclature 134<br/><br/>7.4 Drawing Enantiomers 138<br/><br/>7.5 Diastereomers 143<br/><br/>7.6 Meso Compounds 144<br/><br/>7.7 Drawing Fischer Projections 147<br/><br/>7.8 Optical Activity 152<br/><br/>CHAPTER 8 MECHANISMS 154<br/><br/>8.1 Introduction to Mechanisms 154<br/><br/>8.2 Nucleophiles and Electrophiles 154<br/><br/>8.3 Basicity vs. Nucleophilicity 157<br/><br/>8.4 Arrow-Pushing Patterns for Ionic Mechanisms 159<br/><br/>8.5 Carbocation Rearrangements 164<br/><br/>8.6 Information Contained in a Mechanism 169<br/><br/>CHAPTER 9 SUBSTITUTION REACTIONS 173<br/><br/>9.1 The Mechanisms 173<br/><br/>9.2 Factor 1—The Electrophile (Substrate) 175<br/><br/>9.3 Factor 2—The Nucleophile 178<br/><br/>9.4 Factor 3—The Leaving Group 180<br/><br/>9.5 Factor 4—The Solvent 183<br/><br/>9.6 Using All Four Factors 185<br/><br/>9.7 Substitution Reactions Teach Us Some Important Lessons 186<br/><br/>CHAPTER 10 ELIMINATION REACTIONS 188<br/><br/>10.1 The E2 Mechanism 188<br/><br/>10.2 The Regiochemical Outcome of an E2 Reaction 189<br/><br/>10.3 The Stereochemical Outcome of an E2 Reaction 191<br/><br/>10.4 The E1 Mechanism 194<br/><br/>10.5 The Regiochemical Outcome of an E1 Reaction 195<br/><br/>10.6 The Stereochemical Outcome of an E1 Reaction 196<br/><br/>10.7 Substitution vs. Elimination 196<br/><br/>10.8 Determining the Function of the Reagent 197<br/><br/>10.9 Identifying the Mechanism(s) 199<br/><br/>10.10 Predicting the Products 202<br/><br/>CHAPTER 11 ADDITION REACTIONS 206<br/><br/>11.1 Terminology Describing Regiochemistry 206<br/><br/>11.2 Terminology Describing Stereochemistry 208<br/><br/>11.3 Adding H and H 216<br/><br/>11.4 Adding H and X, Markovnikov 219<br/><br/>11.5 Adding H and Br, Anti-Markovnikov 226<br/><br/>11.6 Adding H and OH, Markovnikov 230<br/><br/>11.7 Adding H and OH, Anti-Markovnikov 233<br/><br/>11.8 Synthesis Techniques 238<br/><br/>11.9 Adding Br and Br; Adding Br and OH 245<br/><br/>11.10 Adding OH and OH, anti 250<br/><br/>11.11 Adding OH and OH, syn 253<br/><br/>11.12 Oxidative Cleavage of an Alkene 255<br/><br/>Summary of Reactions 257<br/><br/>CHAPTER 12 ALKYNES 258<br/><br/>12.1 Structure and Properties of Alkynes 258<br/><br/>12.2 Preparation of Alkynes 261<br/><br/>12.3 Alkylation of Terminal Alkynes 262<br/><br/>12.4 Reduction of Alkynes 264<br/><br/>12.5 Hydration of Alkynes 268<br/><br/>12.6 Keto-Enol Tautomerization 273<br/><br/>12.7 Ozonolysis of Alkynes 279<br/><br/>CHAPTER 13 ALCOHOLS 280<br/><br/>13.1 Naming and Designating Alcohols 280<br/><br/>13.2 Predicting Solubility of Alcohols 281<br/><br/>13.3 Predicting Relative Acidity of Alcohols 283<br/><br/>13.4 Preparing Alcohols: A Review 286<br/><br/>13.5 Preparing Alcohols via Reduction 287<br/><br/>13.6 Preparing Alcohols via Grignard Reactions 294<br/><br/>13.7 Summary of Methods for Preparing Alcohols 298<br/><br/>13.8 Reactions of Alcohols: Substitution and Elimination 300<br/><br/>13.9 Reactions of Alcohols: Oxidation 303<br/><br/>13.10 Converting an Alcohol Into an Ether 305<br/><br/>CHAPTER 14 ETHERS AND EPOXIDES 308<br/><br/>14.1 Introduction to Ethers 308<br/><br/>14.2 Preparation of Ethers 310<br/><br/>14.3 Reactions of Ethers 313<br/><br/>14.4 Preparation of Epoxides 314<br/><br/>14.5 Ring-Opening Reactions of Epoxides 316<br/><br/>CHAPTER 15 SYNTHESIS 323<br/><br/>15.1 One-Step Syntheses 324<br/><br/>15.2 Multistep Syntheses 336<br/><br/>15.3 Retrosynthetic Analysis 337<br/><br/>15.4 Creating Your Own Problems 338<br/><br/>Answer Key 339<br/><br/>Index 371<br/><br/>FEATURES
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chemistry, Organic
General subdivision Study and teaching.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chemistry, Organic
Form subdivision Problems, exercises, etc.
776 08 - ADDITIONAL PHYSICAL FORM ENTRY
Relationship information Online version:
Main entry heading Klein, David R., 1972-
Title Organic chemistry as a second language
Edition 4th edition.
Place, publisher, and date of publication Hoboken : John Wiley & Sons, Inc., [2016]
International Standard Book Number 9781119234524
Record control number (DLC) 2016006248
850 ## - HOLDING INSTITUTION
Holding institution Kuakarun Nursing Library
906 ## - LOCAL DATA ELEMENT F, LDF (RLIN)
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b cbc
c orignew
d 1
e ecip
f 20
g y-gencatlg
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Library of Congress Classification
Koha item type General Book
Koha issues (borrowed), all copies 3
998 ## - STAFF NAME (NMU)
Cataloger ืnuch
Holdings
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    National Library of Medicine Classification     Kuakarun Nursing Library Kuakarun Nursing Library Shelving Cart 20/10/2020 3 2 QD256 K54145 2016 0000045380 11/04/2024 02/04/2024 20/10/2020 General Book