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Organic Chemistry 7EDicon  
รหัส : 9780321610065
ยี่ห้อ : Leroy G. Wade
รุ่น : Prentice Hall
ราคาปกติ :  1,590.00      
ราคาพิเศษ :  1,450.00
เว็บไซต์เกี่ยวข้อง : www.toptextbook.com
รายละเอียดย่อ :
Organic Chemistry:7E
Prentice Hall/Leroy G. Wade
Pearson Education/PP 1328/Soft Cover
Pub Date : Februar 2009
ISBN 9780321610065/0-321-61006-7
รายละเอียดทั้งหมด :

Organic Chemistry:International Edition
Description
For two-semester courses in Organic Chemistry taken primarily by science and pre-health majors.

Organized around functional groups, Wade's text is known for its student-oriented approach-incorporating problem solving help, orientation features, and complete discussions of mechanisms. Wade explains concepts without taking the unnecessary short cuts that often lead to misconceptions.  

Wade's hallmark problem-solving approach includes unique strategies and hints to help students focus on the individual steps of each reaction and how they contribute to the overall reaction. Wade also employs the most pedagogically efficient method of mechanism boxes with its two-tiered approach: Mechanism and Key Mechanism Boxes.  Because there are over 100 mechanisms boxed in every text, Wade delineates the 20 “Key” mechanisms that comprise nearly all of the mechanisms students will encounter.  This means Wade goes one additional and important step in helping students identify and grapple with the smallest number of the most important concepts to understand.

 
Features
CONTENT APPROACH
Clear, consistent presentation of core material is central to a student's success.
  • Complete explanations - Each new topic is introduced carefully and explained thoroughly. Wade explains these topics without taking unnecessary shortcuts that often lead to misconceptions.  This helps students grasp the major concepts and develop flexibility in applying those concepts throughout the course.
THINK BLUE:
Wade uses a color scheme to help students identify each study aid and its purpose. Features in blue help students organize and review the material.
  • First-Exposure icons, a blue pointing hand, indicate the introduction of a reaction students are encountering for the first time.
  • Rules, important insights, and key definitions are highlighted in blue type. These are central to understanding the corresponding chapter material.
  • Mechanism Boxes help students understand how reactions occur by focusing on the individual steps of each reaction. They have large blue headings so students can locate them easily as they thumb through the chapter.
  • Key Mechanism Boxes are the fundamental mechanistic principles that recur throughout the course. They are the mechanisms that compose most of the longer, more complex mechanisms. The spreads include several helpful features:
        -Marked by a key icon indicating their importance in the course
        -Title to clearly describe the type of reaction
        -Steps and descriptions that describe the general nature of the reaction mechanism  (how the reaction occurs)
        -A specific example of the reaction mechanism for reinforcement
        -A concluding problem or question so students can assess their understanding
  • Reaction Summaries help students summarize the characteristics of syntheses and reactions of each functional group and provide students with a “big picture” overview.
THINK GREEN:
Features in green help students get the help they need to solve problems effectively.
  • Problem-Solving Strategies help students break down problems into simpler pieces. These help students methods for approaching complicated problems-like those that require proposing mechanism and developing multi-step synthesis.
  • Problem-Solving Hints are derived from Wade's many years of teaching experience. These hints appear in the margins and remind students of facts or principles that may be useful for solving common types of problems.
  • Essential Problem Solving Skills at the end of every chapter summarize the skills students will need to solve typical problems associated with the chapter's material.
  • Over 1300 (mostly multi-part) problems provide immediate review and reinforcement of the material as students learn it and make sure they understand each section well enough before moving on to the next.
THINK HELP:
The media program available with Wade increases students' understanding and brings organic chemistry to life.
  • NEW! myeBook enables students to make virtual notes within the text, as well as enlarge images, charts, and figures for better viewing 24/7/ Within myeBook students are also able to access Virtual Lectures, where they can see and hear a professor working out the mechanisms and solved problems in the text.
  • NEW! Virtual Lectures, directly linked in myeBook, are professor-narrated videos that provide step-by-step commentary on a virtual whiteboard for all of the mechanisms, key mechanisms, and solved problems throughout the text. These prerecorded videos enable students to pause, rewind, and fast-forward, to individualize their learning.
  • ACE Organic, Pearson's Organic Chemistry Online Homework System-When students draw organic structures, ACE Organic evaluates students' responses and provides feedback to help guide them to the correct answer without giving it away.  The system grades student responses automatically and stores student activity in a gradebook, giving you a better way to track student learning while saving time. www.prenhall.com/aceorganic
THINK IN MULTIPLE DIMENSIONS:
Developing a mental picture of chemical processes is essential for student understanding.
  • The book's design and art program contains state-of-the-art, computer-generated molecular and orbital art.
  • Electrostatic potential maps (EPMs) help students visualize molecules and reactions in ways not possible before by showing calculated charge distributions.
  • Molecular Model Kits allow students to construct their own molecules and see the three dimensional aspects of organic chemistry that can only be imagined on a two dimensional drawing. (Darling Model Kit and Prentice Hall Model Kit)
THINK RELEVANCE
Students find the subject more interesting if they understand how it relates to their major area of study.
  • Biological (and other) applications are found in marginal Applications Notes and throughout the narrative. Students can see the close connection between organic chemistry and areas of interest such as pharmaceutical, industrial, and other biological applications.

 
 
New to this Edition
  • Section 2-14 has been expanded to include hydrogen bonding in amides and water solubility of nitriles.
  • A new Section 8-17 on olefin metathesis, the subject of the 2005 Nobel Prize in Chemistry, covers the basics of the reaction and its mechanism and includes two new in-chapter problems (8-44 and 8-45). 
  • An expanded Section 18-21C now clearly explains the deoxygenation of carbonyl compounds.
  • An expanded Section 9-8 now includes a more explicit description of the differences between the reaction using fused KOH and the reaction using amide ion.
  • A third reaction has been added to Chapter 11, Reaction of Alcohols, to illustrate the conversion of an alcohol to an alkyl halide with phosphorus halides.
  • An expanded Section 15-11 now includes a chemical equation illustrating the Diels-Alder reaction so students can see what the reaction looks like as they read about its useful features.
  • Two new categories (heterocyclic 6p systems and heterocyclic 10p systems) have been added to Section 16-8D, which summarizes the application of Hückel's rule to a variety of cyclic p systems, to further classify the compounds.
  • NEW! myeBook enables students to make virtual notes within the text, as well as enlarge images, charts, and figures for better viewing 24/7/ Within myeBook students are also able to access Virtual Lectures, where they can see and hear a professor working out the mechanisms and solved problems in the text.
  • NEW! Virtual Lectures, directly linked in myeBook, are professor-narrated videos that provide step-by-step commentary on a virtual whiteboard for all of the mechanisms, key mechanisms, and solved problems throughout the text. These prerecorded videos enable students to pause, rewind, and fast-forward, to individualize their learning.
  • A new interior design has been created for this revision.
  • 20% of the end-of-chapter problems have been modified or changed for the Seventh Edition.
  • More Problem-Solving Hints have been added throughout.
  • More glossary entries are provided throughout to help students review and understand the material.
  • Marginal Notes have been added or expanded throughout the text to highlight many additional biological, medical, industrial, and societal uses or organic chemistry.
  • All NMR images spectra are have been converted to high-field resolution spectra. This was done to match the spectra work students will be conducting in the lab and in the workplace.
 
Table of Contents
1     Introduction and Review
2     Structure and Properties of Organic Molecules
3     Structure and Stereochemistry of Alkanes
4     The Study of Chemical Reactions
5     Stereochemistry
6     Alkyl Halides: Nucleophilic Substitution and Elimination
7     Structure and Synthesis of Alkenes
8     Reactions of Alkenes
9     Alkynes
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
19     Amines
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
25    Lipids
26     Synthetic Polymers

Appendices
Answers to Selected Problems
Photo Credits
Index

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