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Neighboring Group Participation

Neighboring Group Participation
Author: Brian Capon
Publisher: Springer Science & Business Media
Total Pages: 285
Release: 2012-12-06
Genre: Science
ISBN: 1468408267

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1. General Considerations.- 1. Introduction.- 1.1. Historical and General Description of Neighboring Group Effects.- 1.2. Terms and Definitions.- 2. Some Factors that Influence Anchimeric Assistance.- 2.1. The Stabilities of Bridged Carbocations-Some Molecular Orbital Calculations.- 2.2 Hyperconjugation-An Alternative Explanation?.- 2.3. The Effect of Intramolecularity-Ring Size and gew-Dialkyl Effects.- 2.3.1. Ring Size.- 2.3.2. The gem-Dialkyl Effect.- 3. Some Experimental Methods Used in the Study of Neighboring Group Participation.- 3.1. Kinetic Methods.- 3.1.1. Estimation of Reaction Rate.


Organic Reactions And Their Mechanisms

Organic Reactions And Their Mechanisms
Author: P S Kalsi
Publisher: New Age International
Total Pages: 668
Release: 2000
Genre: Chemical reactions
ISBN: 9788122412680

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This Revised Edition Includes Several New Topics To Make The Treatment More Comprehensive And Contemporary. The Exposition In Several Chapters Has Also Been Recast To Facilitate An Easier Understanding Of The Subject. * Molecular Orbital And Bonding Thoroughly Explained. * Resonance Structures And Allylic Systems Included. * Organic Acids And Bases Explained In Detail With Additional Examples. * Discussion Of Organic Reactions Considerably Expanded. * Various Additional Dimensions Of Photochemistry Highlighted. * A New Chapter On Special Topics Included.With Its Clear And Systematic Presentation, This Is An Essential Text For B.Sc. And M.Sc. Chemistry Students.


Advanced Organic Chemistry

Advanced Organic Chemistry
Author: Francis A. Carey
Publisher: Springer Science & Business Media
Total Pages: 1216
Release: 2007-06-27
Genre: Science
ISBN: 0387448993

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The two-part, fifth edition of Advanced Organic Chemistry has been substantially revised and reorganized for greater clarity. The material has been updated to reflect advances in the field since the previous edition, especially in computational chemistry. Part A covers fundamental structural topics and basic mechanistic types. It can stand-alone; together, with Part B: Reaction and Synthesis, the two volumes provide a comprehensive foundation for the study in organic chemistry. Companion websites provide digital models for study of structure, reaction and selectivity for students and exercise solutions for instructors.


Organic Mechanisms

Organic Mechanisms
Author: Reinhard Bruckner
Publisher: Springer Science & Business Media
Total Pages: 873
Release: 2010-01-20
Genre: Science
ISBN: 3642036503

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This English edition of a best-selling and award-winning German textbook Reaction Mechanisms: Organic Reactions · Stereochemistry · Modern Synthetic Methods is aimed at those who desire to learn organic chemistry through an approach that is facile to understand and easily committed to memory. Michael Harmata, Norman Rabjohn Distinguished Professor of Organic Chemistry (University of Missouri) surveyed the accuracy of the translation, made certain contributions, and above all adapted its rationalizations to those prevalent in the organic chemistry community in the English-speaking world. Throughout the book fundamental and advanced reaction mechanisms are presented with meticulous precision. The systematic use of red "electron-pushing arrows" allows students to follow each transformation elementary step by elementary step. Mechanisms are not only presented in the traditional contexts of rate laws and substituent effects but, whenever possible, are illustrated using practical, useful and state-of-the-art reactions. The abundance of stereoselective reactions included in the treatise makes the reader familiar with key concepts of stereochemistry. The fundamental topics of the book address the needs of upper-level undergraduate students, while its advanced sections are intended for graduate-level audiences. Accordingly, this book is an essential learning tool for students and a unique addition to the reference desk of practicing organic chemists, who as life-long learners desire to keep abreast of both fundamental and applied aspects of our science. In addition, it will well serve ambitious students in chemistry-related fields such as biochemistry, medicinal chemistry and pharmaceutical chemistry. From the reviews: "Professor Bruckner has further refined his already masterful synthetic organic chemistry classic; the additions are seamless and the text retains the magnificent clarity, rigour and precision which were the hallmark of previous editions. The strength of the book stems from Professor Bruckner’s ability to provide lucid explanations based on a deep understanding of physical organic chemistry and to limit discussion to very carefully selected reaction classes illuminated by exquisitely pertinent examples, often from the recent literature. The panoply of organic synthesis is analysed and dissected according to fundamental structural, orbital, kinetic and thermodynamic principles with an effortless coherence that yields great insight and never over-simplifies. The perfect source text for advanced Undergraduate and Masters/PhD students who want to understand, in depth, the art of synthesis ." Alan C. Spivey, Imperial College London "Bruckner’s ‘Organic Mechanisms’ accurately reflects the way practicing organic chemists think and speak about organic reactions. The figures are beautifully drawn and show the way organic chemists graphically depict reactions. It uses a combination of basic valence bond pictures with more sophisticated molecular orbital treatments. It handles mechanisms both from the "electron pushing perspective" and from a kinetic and energetic view. The book will be very useful to new US graduate students and will help bring them to the level of sophistication needed to be serious researchers in organic chemistry." Charles P. Casey, University of Wisconsin-Madison "This is an excellent advanced organic chemistry textbook that provides a key resource for students and teachers alike." Mark Rizzacasa, University of Melbourne, Australia.