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Organic Chemistry II [MIT Notes2003]
This organic chemistry course note focuses on the methods used to identify the structure of organic molecules, advanced principles of organic stereochemistry, organic reaction mechanisms, and methods used for the synthesis of organic compounds. Major topics covered are: Molecular Formula and Index of Hydrogen Deficiency, Functional Groups, Ethers, Epoxides, and Sulfides, Pericyclic Reactions, Amines, Carboxylic Acids and Derivatives, Enols and Enolates.
Author(s): Dr. Sarah Tabacco and Prof. Timothy F. Jamison
NA Pages 
This textbook is to be used by advanced students of Master's degree programmes specializing in chemistry on core principles of organic chemistry, with key topics including bonding in organic molecules, structural and stereochemical features, and fundamentals of nucleophilic substitution reactions. It further discusses the stereochemistry nature of organic compounds and chemical bonds, which is one of the key areas involved in explaining the behavior of molecules in various chemical reactions. The penetration of the elaboration of various kinds of organic reactions and the theory behind them makes it an indistinguishable resource for students looking to dig deep into the concepts of organic chemistry and its application.
Author(s): Uttarakhand Open University
272 Pages
Organic Chemistry Uttarakhand Open University
This broad spectrum of organic compounds in the textbook encompasses derivatives of hydrocarbons, alcohols, phenols, ethers, epoxides, aldehydes, ketones, and carboxylic acids. The text encompasses functional derivatives of monocarboxylic acids, nitriles, and organosulfur and organophosphorus compounds, based on their chemical behavior and reactivity. It provides comprehensive insights into amino compounds and the various organic reactions occurring within these functional groups. This is the main textbook for students who wish to have mastery over organic chemistry concepts before advanced study or research in it.
Author(s): Uttarakhand Open University
366 Pages