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Organic Chemistry [Hardcover]

G. Marc Loudon (Author)
4.0 out of 5 stars  See all reviews (22 customer reviews)


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Organic Chemistry Organic Chemistry 4.0 out of 5 stars (22)
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Book Description

0195119991 978-0195119992 December 27, 2001 4
With a reputation for outstanding scientific quality, Organic Chemistry by G. Marc Loudon is a textbook that students will actually want to read. This much-anticipated fourth edition continues its predecessors' popular and unique mechanistic approach within a functional group framework. Enhanced biological and biochemical material makes it ideal for chemistry majors as well as pre-medical and pre-pharmacy students taking a full-year, sophomore- level course. Loudon's excellent use of language and reader-friendly style transform organic chemistry into a logical, understandable, and exciting subject for students.

In use at undergraduate and graduate schools of all levels, this authoritative yet accessible volume is packed with effective analogies that enliven and clarify rigorous discussions of important concepts. For example, Loudon uses a flute player jumping between musical octaves to explain transitions between quantum levels. An engaging detective with combined characteristics from Sherlock Holmes and James Bond depicts resonance structures. Thanks to humorous characters like Flick Flaskflinger and Professor Havno Scentz, problem-solving becomes simultaneously challenging and entertaining. Varying from the routine to the complex, Loudon's problems are renowned for their originality, their range of difficulty levels, and their ability to teach students to understand and predict organic reactivity rather than just memorize facts. In addition, Loudon blends biological, environmental, and industrial applications of organic chemistry into the body of the text--rather than separating them as "special topics"--giving students an integrated sense of the subject in its real-life context.

Other Features
� Uses a high-resolution 300 MHz spectra run specifically for this text in an easy-to-read format that makes splitting patterns very clear.
� Includes new sections on transition-metal organometallic chemistry, reactions of pyridoxal phosphate, combinatorial synthesis, and drug design.
� Emphasizes both Bronsted and Lewis acid-base chemistry and their associated curved-arrow notations.
� Provides more than 1,500 excellent in-text problems that challenge students to think and analyze rather than just memorize.
� Presents "boxed asides" with interesting historical vignettes and analogies that enrich the text.
� Utilizes extensive cross-references between important concepts, thus saving students trips to the index.
� Supplemented by a CD-ROM--"Dynamic Organic Chemistry"--containing original animations (Mac and Windows compatible).


Editorial Reviews

Review

"Very easy to understand. Eliminates confusing details and presents the material in plain English, which should catch students' attention."--Cosmas Obi Okoro, Tennessee State University

About the Author

G. Marc Loudon is at Purdue University.

Product Details

  • Hardcover: 1421 pages
  • Publisher: Oxford University Press, USA; 4 edition (December 27, 2001)
  • Language: English
  • ISBN-10: 0195119991
  • ISBN-13: 978-0195119992
  • Product Dimensions: 10.1 x 8.3 x 1.9 inches
  • Shipping Weight: 6.1 pounds
  • Average Customer Review: 4.0 out of 5 stars  See all reviews (22 customer reviews)
  • Amazon Best Sellers Rank: #186,577 in Books (See Top 100 in Books)

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Customer Reviews

22 Reviews
5 star:
 (11)
4 star:
 (5)
3 star:
 (3)
2 star:    (0)
1 star:
 (3)
 
 
 
 
 
Average Customer Review
4.0 out of 5 stars (22 customer reviews)
 
 
 
 
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11 of 11 people found the following review helpful:
5.0 out of 5 stars BEST ORGANIC TEXT, March 6, 2003
By 
Saideh "Sasi" (Pembroke Pines, FL) - See all my reviews
Amazon Verified Purchase(What's this?)
This review is from: Organic Chemistry (Hardcover)
I sold my textbooks that I had used for Organic I (Wade), and Organic II (Solomons) in the middle of the semester and bought this one instead (since our teacher doesn't use the book, only his notes). I found this book so much easier to learn from. Especially for someone who has had trouble learning the subject.
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7 of 7 people found the following review helpful:
3.0 out of 5 stars Good, but not good enough, October 31, 2004
By 
A. Christopher (West Lafayette, IN USA) - See all my reviews
(REAL NAME)   
Amazon Verified Purchase(What's this?)
This review is from: Organic Chemistry (Hardcover)
This is a great introductory textbook for organic chemistry, but for accelerated chemistry courses, it simply failed to give more advanced materials and examples.
I ended up getting another organic chemistry textbook to complement it. Still one of the most understandable organic textbook around, though.
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6 of 6 people found the following review helpful:
5.0 out of 5 stars This is the best organic text!, September 5, 2002
By 
This review is from: Organic Chemistry (Hardcover)
This is my favorite chemistry book. This book is different from others because it's conversational in tone and easy to read. If more chemists wrote like this, there would be a lot fewer discouraged potential chemists out there. The electron diagrams lead to complete understanding of reactions so you don't need to memorize them. The problems are interesting puzzles. You will want to do more than the ones that are assigned just to find out what the answer is. The accompanying solution manual provides all the details needed to completely understand the answers. Chemistry can be beautiful and understandable when a book is written this well.
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Inside This Book (learn more)
First Sentence:
Organic chemistry is the branch of science that deals generally with compounds of carbon. Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
following study problem, more branched carbon, chemically nonequivalent sets, noncongruent mirror images, principal organic product, hydrogen halide addition, tetrahedral addition intermediate, flagpole hydrogens, benzamidinium ion, enolate ions derived, pericyclic selection rules, substitutive nomenclature, one alkene product, important resonance structures, dialkylcuprate reagents, following alkyl halides, substitutive name, isobutyl cation, unshared valence electrons, alkenes into alcohols, acetylenic anions, alkene starting material, indicated starting material, more stable carbocation intermediate, multiplicative splitting
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Nobel Prize, United States, Reaction Review, Solution First, Emil Fischer, Chemical Abstracts, University of California, Solving Structure Problems, Purdue University, California Institute of Technology, Cornell University, Georg Wittig
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