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Organic Chemistry, 8th Edition by Francis A. Carey, Robert M. Giuliano free pdf download

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 Organic Chemistry, 8th Edition by Francis A. Carey, Robert M. Giuliano.


Organic Chemistry, 8th Edition by Francis A. Carey, Robert M. Giuliano

Contents:
1 Structure Determines Properties 
 2 Alkanes and Cycloalkanes: Introduction to Hydrocarbons
 3 Alkanes and Cycloalkanes: Conformations and cis-trans Stereoisomers
 4 Alcohols and Alkyl Halides
 5 Structure and Preparation of Alkenes: Elimination Reactions
 6 Addition Reactions of Alkenes
 7 Stereo chemistry
 8 Nucleophilic Substitution
 9 Alkynes
 10 Conjugation in Alkadienes and Allylic Systems
 11 Arenes and Aromaticity
 12 Reactions of Arenes: Electrophilic and Nucleophilic Aromatic Substitution
 13 Spectroscopy
 14 Organometallic Compounds
 15 Alcohols, Diols, and Thiols
 16 Ethers, Epoxides, and Sulfi des
 17 Aldehydes and Ketones: Nucleophilic Addition to the Carbonyl Group
 18 Carboxylic Acids
 19 Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution
 20 Enols and Enolates
 21 Amines
 22 Phenols
 23 Carbohydrates
 24 Lipids
 25 Amino Acids, Peptides, and Proteins
 26 Nucleosides, Nucleotides, and Nucleic Acids
 27 Synthetic Polymers
Glossary G-1
Credits C-1
Index

What Sets This Book Apart?
The central message of chemistry is that the properties of a substance come from its structure. What is less obvious, but very powerful, is the corollary. Someone with training in chemistry can look at the structure of a substance and tell you a lot about its properties. Organic chemistry has always been, and continues to be, the branch of chemistry that best connects structure with properties.

 The goal of this text, as it has been through seven previous editions, is to provide students with the conceptual tools to understand and apply the relationship between the structures of organic compounds and their properties. Both the organization of the text and the presentation of individual topics were designed with this objective in mind.

A Functional Group Organization
The text is organized according to functional groups—structural units within a molecule that are most closely identified with characteristic properties. This organization offers two major advantages over alternative organizations based on mechanisms or reaction types.
1. The information content of individual chapters is more manageable when organized according to functional groups.

2. Patterns of reactivity are reinforced when a reaction used to prepare a particular functional group reappears as a characteristic reaction of a different functional group. 

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