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2009 Hardcover Good Item may show signs of shelf wear. Pages may include limited notes and highlighting. Includes supplemental or companion materials if applicable. Access ...codes may or may not work. Connecting readers since 1972. Customer service is our top priority.Read moreShow Less
Organized around functional groups, this book incorporates problem-solving help, orientation features, and complete discussions of mechanisms. Wade explains concepts without taking the unnecessary short cuts that often lead to misconceptions—his hallmark problem-solving approach includes unique strategies and hints to help readers focus on the individual steps of each reaction and how they contribute to the overall reaction. Wade also employs the most efficient method of mechanism boxes with its two-tiered approach: Mechanism and Key Mechanism Boxes. He delineates the 20 “Key” mechanisms that comprise nearly all of the mechanisms students will encounter. Therefore, the book takes one additional and important step in helping readers identify and grapple with the smallest number of the most important concepts to understand.
Acid-Base Chemistry, Lewis Structures, Bronsted, Electron Structure (shell, orbitals, magnetic shielding), Bonding (formation, patterns, polarity, MO), Resonance, Stereochemistry, MO Theory, Conformational analysis, Thermodynamics, Kinetics, Reaction Coordinate diagrams, Chirality, Regioselectivity, Synthesis, Aromaticity, Carbonyl chemistry.
A comprehensive reference for chemistry professionals.
New edition of a text that covers the fundamentals of organic chemistry, including both the classical reactions and the new techniques and reactions in current use by practicing chemists. New sections address free-radical inhibitors, using the Mislow and Siegel definition, the asymmetric reduction work by Noyori and Knowles, the Sharpless asymmetric epoxidation, the aromaticity of Fullerenes and their relationship to other allotropes of carbon, prions, and others. Visual aids comprise boxes containing information on important mechanisms, and electrostatic potential maps. Annotation c. Book News, Inc., Portland, OR
New edition of a text first published in 1987. The text has been microedited, with many large passages rewritten to enhance clarity. Annotation c. Book News, Inc., Portland, OR (booknews.com)
L.G. “Skip” Wade decided to become a chemistry major during his sophomore year at Rice University, while taking organic chemistry from Professor Ronald M. Magid. After receiving his B.A. from Rice in 1969, Wade went on to Harvard University, where he did research with Professor James D. White. While at Harvard, he served as the Head Teaching Fellow for the organic laboratories and was strongly influenced by the teaching methods of two master educators, Professors Leonard K. Nash and Frank H. Westheimer.
After completing his Ph.D. at Harvard in 1974, Dr. Wade joined the chemistry faculty at Colorado State University. Over the course of fifteen years at Colorado State, Dr. Wade taught organic chemistry to thousands of students working toward careers in all areas of biology, chemistry, human medicine, veterinary medicine, and environmental studies. He also authored research papers in organic synthesis and in chemical education, as well as eleven books reviewing current research in organic synthesis. Since 1989, Dr. Wade has been a chemistry professor at Whitman College, where he teaches organic chemistry and pursues interests in organic synthesis and forensic chemistry. Dr. Wade received the A.E. Lange Award for Distinguished Science Teaching at Whitman in 1993.
Dr. Wade’s interest in forensic science has led him to testify as an expert witness in court cases involving drugs and firearms, and he has worked as a police firearms instructor, drug consultant, and boating safety officer. He also enjoys repairing and restoring old violins and bows, which he has done professionally for many years.
1 Introduction and Review
2 Structure and Properties of Organic Molecules
3 Structure and Stereochemistry of Alkanes
4 The Study of Chemical Reactions
6 Alkyl Halides: Nucleophilic Substitution and Elimination
7 Structure and Synthesis of Alkenes
8 Reactions of Alkenes
10 Structure and Synthesis of Alcohols
11 Reactions of Alcohols
12 Infrared Spectroscopy and Mass Spectrometry
13 Nuclear Magnetic Resonance Spectroscopy
14 Ethers, Epoxides, and Sulfides
15 Conjugated Systems, Orbital Symmetry, and Ultraviolet Spectroscopy
16 Aromatic Compounds
17 Reactions of Aromatic Compounds
18 Ketones and Aldehydes
20 Carboxylic Acids
21 Carboxylic Acid Derivatives
22 Condensations and Alpha Substitutions of Carbonyl Compounds
23 Carbohydrates and Nucleic Acids
24 Amino Acids, Peptides, and Proteins
26 Synthetic Polymers
Appendices Answers to Selected Problems Photo Credits Index