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• The Chemical Shift. Spin-Spin Coupling. The Analysis of NMR Spectra. Pulse Fourier Transform Techniques. Double Resonance Techniques and Relaxation Mechanisms. Multipulse NMR Techniques and Two-Dimensional NMR. Applications of NMR Spectroscopy. Problems. Subject Index.
• (source: Nielsen Book Data)

Introduction to NMR Spectroscopy R. J. Abraham, School of Chemistry, University of Liverpool J. Fisher, Biological NMR Centre, University of Leicester P. Loftus, Stuart Pharmaceuticals, Delaware, USA This book is a new, extended edition of Proton and Carbon 13 NMR by R. J. Abraham and P. Loftus. The initial chapters cover the fundamentals of NMR spectroscopy commencing with an explanation of how the nuclear magnetic response occurs, followed by a detailed discussion of chemical shifts and coupling constants, parameters not discussed to any length in other textbooks aimed at a similar level of interest. Emphasis is given to the vectorial description of multipulse experiments, as this is probably the easiest way to grasp how different information may be gained simply by changing a pulse sequence. An understanding of multipulse NMR is a prerequisite for understanding 2D NMR. The section on 2D NMR begins with a discussion of the resolved experiment. This is a logical initial choice as the spectra produced by this experiment may be readily compared with 1D spectra. Following on from this both heteronuclear and homonuclear correlation spectroscopy are described and examples given. The final section of the book should be considered as an applications section. It is aimed at showing the reader that NMR is not just of use to the synthetic organic chemist but is also of use to biochemists for investigating the solution state structure and function of proteins, enzymes, etc. The application of high resolution NMR to the solid state is also discussed, thereby indicating the developments which have taken place as far as spectrometer hardware is concerned.
(source: Nielsen Book Data)

• I. Introduction, alcohols, yeast, malt and malt liquors, wines and potable spirits, neutral alcohol derivatives, sugars, starch and its isomerides, paper and pulp testing, aliphatic acids.- II. Fixed oils, fats and waxes, special characters and methods, butter fat, lard,linseed oil, higher fatty acids, soap, glycerin, wool-fat, cloth oils, sterol alcohols.- III. Hydrocarbons, bitumens, naphthale and its derivatives, anthracene and its associates, phenols, aromatic acids, gallic acid, and its allies, phthalic acid and the phthaleins, modern explosives.- IV. Special characters of essential oils; resins, india-rubber, gutta percha, balata, and allied substances; the constituents of essential oils, and allied substances; the general characters and analysis of essential oils.- V. Tannins, writing inks, stamping, typing and marking inks, printing inks, amines and ammonium bases, analysis of leather, colouring matters of natural origin, colouring substances in foods, benzene and its homoloues, aniline and its allies, naphthylamines, pyridine, quinoline and acridine bases.-

• I. Introduction, alcohols, yeast, malt liquors and malt, wines and spirits, neutral alcoholic derivatives, sugars, starch and its isomerides, paper and paper-making materials, vegetable acids
• II. Fixed oils, fats and waxes; special characters and methods, butter fat, lard, linseed oil, higher fatty acids, soap, glycerol, cholesterols, wool-fat, cloth oils
• III. Hydrocarbons, bitumens, naphthalene and its derivatives, anthracene and its associates, phenols, aromatic acids, gallic acid and its allies, phthalic acid and the phthaleins, modern explosives
• Iv. Resins, india-rubber, rubber substitutes and gutta-percha, hydrocarbons of essential oils, ketones of essential oils, volatile or essential oils, special characters of essential oils, tables of essential oils
• v. Tannins, analysis of leather, dyes and colouring matters, dyestuffs of groups 6 to 12, colouring matters of natural origin, analysis of colouring matters, colouring matters in foods, inks
• VI. Amines and ammonium bases, aniline and its allies, naphthylamines, pyridine, quinoline and acridine bases, vegetable alkaloids, volatile bases of vegetable origin, nicotine and tobacco, aconite alkaloids, atropine and its allies, cocaine, opium, strychnos alkaloids, cinchona alkaloids, berberine, caffeine, tea and coffee, cocoa and chocolate
• VII. Vegetable alkaloids, glucosides, non-glucosidal bitter principles, animal bases, animal acids, lactic acid, cyanogen and its derivatives
• VIII. Enzymes, proteins and albuminoid substances, milk and milk products, meat and meat products, hæmoglobin and blood, proteoids, fibroids
• IX. Supplement, index to series.

• Partial table of contents: The Rules of the Game. Slow Motion, Deep Insight. Clear Drawings, Three--Dimensional Structures. Preserve Atoms in Place, Keep Things Simple. Atom and Bond Budgets. Fragmentation of Bicyclobutane by Way of Anti--Bredt Intermediates. Acidic Fragmentation in the Course of a Clever Synthesis of Alpha----Methylene Butyrolactones. A Local Oxidation at the Unexpected Site by Bromination at the Expected Site. Vicinal Migrations with Stereocontrol. Hydrazine Used for Ring Mutation. A Stepwise Electron Transfer That Requires Two Moles of Oxidant. Circuitous Oxidation With Lead Tetraacetate. Multifaceted Performance of Grignard Reagent. A Potentially Complex Wagner----Meerwein Rearrangement Made Simple. Strange Involvement of Nonfunctionalized Isopentyl Side Chain. A Case of X--Ray Data Yielding the Wrong Structure Due to Interference of Organic Chemistry. Reaction Index.
• (source: Nielsen Book Data)

For students of advanced organic chemistry, this text develops problem-solving skills using fifty-six challenging, organic chemistry problems covering a wide variety of chemical systems. Concentrates on necessary and fundamental concepts in the introductory chapters. Valuable not only as a study guide and source of interesting problems, but also as an illustration of reactions and phenomena of general interest.
(source: Nielsen Book Data)

• pt.
• 1. Direct methods.--pt.
• 2. Indirect methods.

• Part 1 Laboratory operations: preliminary topics
• separation of substances
• purification of substances
• determination of physical properties
• determination of chemical properties
• qualitative organic analysis
• apparatus and techniques for chemical reactions. Part 2 Experiments: separations
• transformations
• synthetic sequences - synthesis experiments that use a sequence of reactions.
• (source: Nielsen Book Data)

Ideally suited for second-year undergraduate organic chemistry laboratory courses, this text explains how to perform operations and prepare a variety of organic compounds. As they learn how to filter a hot solution, recrystallize a solid, distil a liquid, perform an extraction and dry a solution, students will come to understand the theory behind the techniques. The book includes substitutions, additions, eliminations and 'name' reactions such as the Grignard reaction and the Wittig synthesis as well as procedures for the preparation of interesting compounds such as aspirin and the alarm pheromone of the honey bee.
(source: Nielsen Book Data)

• Acknowledgements.Preface.
• Chapter 1. Quantum Mechanics for Organic Chemistry .
• Chapter 2. Fundamentals of Organic Chemistry.
• Chapter 3. Pericyclic Reactions.
• Chapter 4. Diradicals and Carbenes.Chapter 5.Organic Reactions of Anions.
• Chapter 6. Solution-Phase Organic Chemistry.
• Chapter 7. Organic Reaction Dynamics.
• (source: Nielsen Book Data)

'[This book] collects together, largely for the first time, a series of chapters dedicated to all the ways in which molecular modeling/computational chemistry can impact organic chemistry' - Christopher J. Cramer, author of "Essentials of Computational Chemistry: Theories and Models". "Computational Organic Chemistry" provides a practical overview of the ways in which computational modeling methods and applications can be used in organic chemistry to predict the structure and reactivity of organic molecules. After a concise survey of computational methods, the book presents in-depth case studies that show how various computational methods have provided critical insight into the nature of organic mechanisms. With a focus on methodologies, this unique resource: discusses simple molecular properties, pericyclic reactions, carbenes and radicals, anion chemistry, solvent effects, and more; features sidebars that offer a personal look at some of the leading practitioners in the field; conveys the strengths and limitations of each method, so that readers develop a feel for the correct 'tool' to use in the context of a specific problem; and, further informs readers with a supporting Web site that provides links to materials cited and features a blog that discusses and provides links to new relevant articles. This is a great reference for practicing physical organic and computational chemists, as well as a thought-provoking textbook for graduate-level courses in computational chemistry and organic chemistry.
(source: Nielsen Book Data)

• The alkanes
• the alkenes
• the alkynes
• the arenes
• halo-alkanes
• Grignard and alkyllithium reagents
• hydroxyl compounds
• ethers
• epoxides
• thiols and thioethers
• the carbonyl group
• unsaturated carbonyl compounds
• amines
• carbohydrates
• carboxylic acids
• carboxylic esters
• amides
• acyl halides
• acid anhydrides
• cyanides (nitriles)
• bifunctional acids and esters
• amino acids peptides
• carbonic acids and their derivatives
• sulphoxides and sulphones
• sulphonic acids and their derivatives
• nitro compounds
• carbon-nitroso compounds
• heterocyclic compounds
• basic organic photochemistry
• appendices - some approximate chemical shift ranges for different groups, NMR data for some common deuterated solvents, some typical values for I.R. vibrational frequencies.
• (source: Nielsen Book Data)

This text is designed to provide first-year students with a concise guide to the important general reactions of organic chemistry, which form the foundation of all later work. The book should enable students to understand organic reactions and the inter-relationship between organic compounds.
(source: Nielsen Book Data)

This book is about the recognition of new principles in Organic Chemistry. It is also about the discovery and invention of Chemical Reactions. In addition, it deals with the determination of structure by chemical degradation during the epoch when physical methods were not well developed. Also presented are new reagents and new types of functional groups never seen in chemistry before. The overall aim of the collected papers is to show how thought can direct original research and to demonstrate how thought about old or new chemical facts can lead to originality. This is further illuminated by commentaries which Prof Barton has written to accompany these papers.
(source: Nielsen Book Data)

Nobel Laureate Sir Derek Barton discusses his scientific career, which embraced tenures as Professor at Imperial College, London for 20 years before becoming Director of Research at the CNRS at Gif-sur-Yvette, France for a decade, and now professor at Texas A and M University. Barton highlights his work in natural products synthesis and structure identification, his development of novel synthetic reactions, and his recent research in radical chemistry. His volume is laced with numerous anecdotes about many famous chemists and contains 49 photographs.
(source: Nielsen Book Data)

• V. 1. Chemistry of organosilicon compounds.
• v. 2. Register of organosilicon compounds. 2 v.

• 1. Abt. Einleitung. Specieller Theil: Fettreihe.
• 2. Abt. Specieller Theil: aromatische Reihe.

An invaluable teaching tool now back in print, the book traces the transformation of organic chemistry from 1800 to Couper and Kekule, noting gaps in their structural theories that were filled in by later chemists.
(source: Nielsen Book Data)