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Anodic Oxidation covers the application of the concept, principles, and methods of electrochemistry to organic reactions. This book is composed of two parts encompassing 12 chapters that consider the mechanism of anodic oxidation. Part I surveys the theory and methods of electrochemistry as applied to organic reactions. These parts also present the mathematical equations to describe the kinetics of electrode reactions using both polarographic and steady-state conditions. Part II examines the anodic oxidation of organic substrates by the functional group initially attacked. This part particularly emphasizes the kinds of intermediates generated and the mechanisms leading to final products. This book is intended primarily to organic chemists and physical electrochemists.
Cyclophanes, Volume I is a collection of papers that reviews cyclophane chemistry. One paper describes the genesis of the cyclophane concept, covering its past, present, and future possible applications. The results of experimental and theoretical studies show the interrelationships between the structure and energetics in the class of compounds known as cyclophanes. Another paper relates the X-ray crystal structure determinations of cyclophanes to set the crystallographic and structural data of these systems in such a form that will enable comparisons, lead to an understanding of the geometries and deviations, and open the application of data to other areas of cyclophane chemistry. One paper...
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Organic Chemistry, Second Edition, Volume I: Organic Functional Group Preparations provides a convenient and useful source of reliable preparative procedures for the most common functional groups. This book discusses the preparations of each group that are subdivided into different reaction types, including elimination, condensation, and oxidation and reduction reactions. Organized into 21 chapters, this edition begins with an overview of the reduction methods that allow the preparation of hydrocarbon of known structure. This text then explores the acid-catalyzed of thermal elimination of water from alcohols, which is a common laboratory method for the preparation of olefins. Other chapters consider the two most significant synthetic methods for introducing an acetylenic group into the molecule, which involve the elimination of hydrogen halides. This book discusses as well the importance of oxidation reactions. The final chapter deals with sulfonation reactions. This book is a valuable resource for organic chemists and research workers.
First multi-year cumulation covers six years: 1965-70.
Cyclophanes, Volume II, provides a comprehensive review of the field of cyclophane chemistry for the period between the earlier volume in this series (Bridged Aromatic Compounds by A. H. Smith, 1964) and the present (generally through 1981). An attempt has been made to provide a selection of topics that delineate the past and present of cyclophane chemistry and point toward some of its future directions. The ordering of chapters has been chosen to present background, theory, structure, and spectroscopy followed by a somewhat arbitrary division of cyclophanes into subgroups, roughly in order of increasing structural complexity. Key topics discussed include the synthesis and properties of heterophanes, condensed benzenoid and nonbenzenoid cyclophanes, multibridged and multilayered cyclophanes, cyclophanes in host-guest chemistry, and cyclophanes as synthetic analogs of enzymes and receptors. Individual chapters have been written so that they may be read with little or no direct reference to other chapters. Each stands alone as a review of a particular area of cyclophane chemistry and therefore some overlap between chapters will be apparent.
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Polymer Syntheses, Volume III provides useful polymer synthesis information. The book discusses the olefin-sulfur dioxide copolymers; the polythioesters; and sulphide polymers. The text also describes polymerizations reactions of mono and diisocyanates; polyoxyalkylation of hydroxyl compounds; and polymerization reactions of N-vinyl carbazole and related monomers. The polymerization of vinyl acetate and other vinyl esters; the polymerization of allyl esters; and the polymerization of vinyl fluoride are also considered. The book further tackles miscellaneous polymer preparations.
Carbon-13 NMR Spectroscopy focuses on the potential of 13C techniques and the practical difficulties associated with the detection of 13C NMR absorption. This monograph includes a descriptive presentation of 13C shielding results that has been adopted with emphasis on the structural and stereochemical aspects. Organized into four parts encompassing 11 chapters, this book starts with an overview of the characteristics of the NMR signals derived from compounds containing 13C nuclei in natural abundance that are inherently much weaker than those exhibited by protons. This monograph then compares the primary characteristics of 13C NMR with the more familiar proton methods. Other chapters consider the 13C spectra of pyridine, pyridazine, pyrimidine, pyrazine, s-triazine, and s-tetrazine. The final chapter deals with the effects of solute–solvent interactions on the shieldings of other nuclei. This monograph is intended for organic chemists, graduate students, and researchers in various branches of chemistry with an interest in 13C NMR methods as another approach to chemical problems.
Organic Functional Group Preparations, Volume III describes 13 organic functional groups and presents a critical review of their available methods of synthesis with preparative examples of each. The book puts special attention to the presentation of specific laboratory directions for the many name reactions used in describing the synthesis of these functional groups. Each chapter deals with the preparation of a given functional group by various reaction types (condensation, elimination, oxidation, reduction) and a variety of starting materials. Acetals and ketals, anhydrides, and thiohydroxamic acids are some of the organic functional groups described in the text. Organic chemists will find the book invaluable.