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|a 547
|2 23
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| 100 |
1 |
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|a Karty, Joel,
|e author.
|0 http://id.loc.gov/authorities/names/n2005012715
|
| 245 |
1 |
0 |
|a Organic chemistry :
|b principles and mechanisms /
|c Joel M. Karty.
|
| 250 |
|
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|a Second edition.
|
| 264 |
|
1 |
|a New York ;
|a London :
|b W.W. Norton,
|c [2018]
|
| 300 |
|
|
|a l, 1,369, 161 variously numbered pages :
|b illustrations (some color) ;
|c 28 cm
|
| 336 |
|
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|a text
|b txt
|2 rdacontent
|
| 337 |
|
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|a unmediated
|b n
|2 rdamedia
|
| 338 |
|
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|a volume
|b nc
|2 rdacarrier
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| 504 |
|
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|a Includes bibliographical references and index.
|
| 505 |
0 |
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|a Atomic and molecular structure -- Interchapter A: Nomenclature: the basic system for naming organic compounds: alkanes, haloalkanes, nitroalkanes, cycloalkanes, and ethers -- Three-dimensional geometry, intermolecular interactions, and physical properties -- Orbital interactions 1: hybridization and two-center molecular orbitals -- Interchapter B: Naming alkenes, alkynes, and benzene derivatives -- Isomerism 1: conformers and constitutional isomers -- Isomerism 2: chirality, enantiomers, and diastereomers -- Interchapter C: Stereochemistry in nomenclature: R and S configurations about asymmetric carbons and Z and E configurations about double bonds -- The proton transfer reaction: an introduction to mechanisms, thermodynamics, and charge stability -- An overview of the most common elementary steps -- Interchapter D: molecular orbital theory, hyperconjugation, and chemical reactions -- Interchapter E: naming compounds with a functional group that calls for a suffix 1: alcohols, amines, ketones, and aldehydes -- An introduction to multistep mechanisms: SN1 and E1 reactions and their comparisons to SN2 and E2 reactions -- Nucleophilic substitution and elimination reactions 1: competition among SN2, SN1, E2, and E1 reactions -- Interchapter F: naming compounds with a functional group that calls for a suffix 2: carboxylic acids and their derivatives -- Nucleophilic substitution and elimination reactions 2: reactions that are useful for synthesis -- Electrophilic addition to nonpolar bonds 1: addition of a bronsted acid -- Electrophilic addition to nonpolar bonds 2: reactions involving cyclic transition states -- Organic synthesis 1: beginning concepts in designing multistep synthesis -- Orbital interactions 2: extended systems, conjugation, and aromaticity -- Structure determination 1: ultraviolet-visible and infared spectroscopies -- Structure determination 2: nuclear magnetic resonance spectroscopy and mass spectrometry -- Nucleophilic addition to plar bonds 1: addition of stron nucleophiles -- Nucleophilic addition to polar bonds 2: weak nucleophiles and acid and bas catalysis -- Organic synthesis 2: intermediate topics in synthesis design, and useful redox and carbon-carbon bond-forming reactions -- Nucleophilic addition-elimination reactions 1: the general mechanism involving strong nucleophiles -- Nucleophilic addition-elimination reactions 2: weak nucleophiles -- Aromatic substitution 1: electrophilic aromatic substitution on benzene; useful accompanying reactions -- Aromatic substitution 2: reactions of substituted benzenes and other rings -- The diels-alder reaction and other pericyclic reactions -- Reactions involving free radicals -- Interchapter G: fragmentation pathways in mass spectrometry -- Polymers
|
| 650 |
|
0 |
|a Chemistry, Organic
|v Textbooks.
|0 http://id.loc.gov/authorities/subjects/sh2009118860
|
| 650 |
|
7 |
|a Chemistry, Organic.
|2 fast
|0 (OCoLC)fst00853501
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|p 2 Hour Loan
|a Michigan State University-Library of Michigan
|b Michigan State University
|c MSU Main Library
|d MSU Digital Reserves
|t 0
|e QD253.2 .K375 2018
|h Library of Congress classification
|i Electronic Resource
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