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Organic Chemistry (7th Edition) Review

To succeed with this book, make sure that you do all of the in-text problems at a minimum, in addition to whatever other assigned homework you get. I used the book for a class, but I would say that it's very good for self-study, because the in-text problems really help make sure that you're being an active reader and not just zombie-ing through the pages, and the solutions manual contains solutions to ALL problems, not just the odds. And when you're memorizing the reactions, probably the best way to do it is to use flashcards. One one side have the reagents on the left, draw an arrow, and have a question mark on the right for the products. On the other side, have the reagent, an arrow towards the products, and a question mark over the arrow. This ensures that you know the reaction inside and out.
One think another reviewer suggested that I agree with would be to add expected yields for reactions. Or an appendix of some of them, if it's thought that including them in early reactions might cause confusion.
EDIT: After finishing my second semester of organic chemistry, I have to say that I really agree with the reviewer I had previously mentioned, in that the book does get very repetitive in the last few chapters before the biochemistry. And there's not very many real synthesis questions. The majority of the "synthetic conversion" problems are two or three steps at most. But overall, this book is still very clear, and a good learning resource.

Organic Chemistry (7th Edition) Overview

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.

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