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140122 ||| eng |
020 |
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|a 9781475711431
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100 |
1 |
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|a Carey, Francis A.
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245 |
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|a Advanced Organic Chemistry
|h Elektronische Ressource
|b Part A: Structure and Mechanisms
|c by Francis A. Carey
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250 |
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|a 1st ed. 1984
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260 |
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|a New York, NY
|b Springer US
|c 1984, 1984
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300 |
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|a XVIII, 726 p. 169 illus
|b online resource
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|a Chemical Bonding and Molecular Structure -- Stereochemical Principles -- Conformational, Steric, and Stereoelectronic Effects -- Study and Description of Organic Reaction Mechanisms -- Nucleophilic Substitution -- Polar Addition and Elimination Reactions -- Carbanions and Other Nucleophilic Carbon Species -- Reactions of Carbonyl Compounds -- Aromaticity and Electrophilic Aromatic Substitution -- Concerted Reactions -- Photochemistry -- Free-Radical Reactions
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653 |
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|a Chemistry, Organic
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653 |
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|a Organic Chemistry
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|a eng
|2 ISO 639-2
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|b SBA
|a Springer Book Archives -2004
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028 |
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|a 10.1007/978-1-4757-1143-1
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|u https://doi.org/10.1007/978-1-4757-1143-1?nosfx=y
|x Verlag
|3 Volltext
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|a 547
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|a The purpose of this edition is the same as that of the first edition, that is, to provide a deeper understanding of the structures of organic compounds and the mechanisms of organic reactions. The level is aimed at advanced undergraduates and beginning graduate students. Our goal is to solidify the student's understanding of basic concepts provided in an introduction to organic chemistry and to fill in much more information and detail, including quantitative information, than can be presented in the first course in organic chemistry. The first three chapters consider the fundamental topics of bonding theory, stereochemistry, and conformation. Chapter 4 discusses the techniques that are used to study and characterize reaction mechanisms. The remaining chapters consider basic reaction types with a broad coverage of substituent effects and stereochemistry being provided so that each reaction can be described in good, if not entirely complete, detail. The organization is very similar to the first edition with only a relative shift in emphasis having been made. The major change is the more general application of qualitative molecular orbital theory in presenting the structural basis of substituent and stereoelectronic effects. The primary research literature now uses molecular orbital approaches very widely, while resonance theory serves as the primary tool for explanation of structural and substituent effects at the introductory level. Our intention is to illustrate the use of both types of interpretation, with the goal of facilitating the student's ability to understand and apply the molecular orbital concepts now widely in use
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