Organic Chemistry, 10/e (IE-Paperback)
暫譯: 有機化學，第10版 (IE-平裝本)

Leroy G. Wade and Jan W. Simek

Organic Chemistry, 10/e (IE-Paperback)

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本書序言

•28Focus Features help focusstudents on analyzing key aspects of complex topics and reactions.
•Marginboxes featuring details about the lives and works of eminent scientists
Pearson eText is a simple-to-use,mobile-optimized, personalized reading experience available within Mastering.It allows students to easily highlight, take notes, and review key vocabularyall in one place, even when offline. Seamlessly integrated videos and other richmedia engage students and give them access to the help they need, when theyneed it.
• Digitized versions of Visual Guides to Organic Reactions and Key Mechanism Boxes include videos and can be accessed through links in the eText, giving students easy access to visual explanations of mechanisms, nomenclature, and reaction summaries. Videos are also available in Mastering Chemistry.
Highlights of the Update forMastering Chemistry
• Key Mechanism and Mechanism Overview Videos are created as paired videos. Each key mechanism is covered first in an overview video that outlines the type of mechanism and the necessary background for understanding what is taking place. Then, a second video walks the students through a representative reaction of that key mechanism.
• Mechanism Practice Problems feature one-step hints and predict the product functionality on any step of selected problems if they struggle. The problems give students a place to learn through practice and to earn credit based upon completion rather than correct answers.
• Item Library is curated, reclassified, and organized into four tiers to help instructors to navigate resources in Mastering Chemistry,
• Tier 1 includes practice questions with credit for completion.
• Tier 2 includes predict the product and single-step mechanisms
• Tier 3 includes new multi-step mechanisms with hints and multi-step problems with the number of boxes and/or intermediates.
• Tier 4 includes synthesis questions.
• Ready-to-Go Study Tools are available for students to use on their own, even when their professor doesnt assign the modules. These include videos, practice quizzes, practice exams, and worked examples.

本書特色

• Problem-Solving Strategies help students break down the multitude of complex problems into simpler pieces and establish thoughtful methods for approaching complicated problems. Strategies cover resonance, acid-base equilibria, and multistep synthesis.
• Over 100 problems include synthesis problems and problems based on recent literature.
Helpstudents see the relevance of organic chemistry
• Green chemistry is emphasized with presentation of less-toxic, environmentally friendly reagents in many situations, such as oxidation of alcohols with bleach rather than with chromium reagents.
• Chapter Openers focus on applications discussed in the chapter, with introductions and images for a contemporary presentation.
• Application Boxes throughout demonstrate the relevance of Organic Chemistry to students lives and areas of interest including contemporary topics such as Biochemistry, Drugs, Environment, Medicine, Fuels, Green Chemistry and Green Living.
Emphasizeorganic reactions and mechanisms
• Reaction Starbursts appear before the end of chapter material of every reaction-based chapter to help students better understand and mentally organize reactive similarities and distinctions.
• Visual Guides to Organic Reactions place the reactions covered in major chapters within the overall context of the reactions covered in the course.
• 20 Key Mechanism boxes highlight the fundamental mechanistic principles that recur throughout the course and are the basis for some of the longer, more complex mechanisms. Each describes the steps of the reaction in detail with a specific example to reinforce the mechanism and a concluding problem to help students absorb these essential reactions.
• Over 50 Mechanism boxes help students understand how specific reactions occur by zooming in on each individual step in detail.

商品描述(中文翻譯)

本書序言

• 28個焦點特徵幫助學生專注於分析複雜主題和反應的關鍵方面。

• 邊欄框展示著名科學家的生活和作品的詳細資訊。

Pearson eText 是一個簡單易用、針對行動裝置優化的個性化閱讀體驗，內建於 Mastering 中。它允許學生輕鬆地標註重點、做筆記，並在一個地方回顧關鍵詞彙，即使在離線狀態下也能使用。無縫整合的影片和其他豐富媒體吸引學生，並在他們需要時提供所需的幫助。

• 數位化的有機反應視覺指南和關鍵機制框包含影片，並可通過 eText 中的連結訪問，讓學生輕鬆獲得機制、命名法和反應摘要的視覺解釋。影片也可在 Mastering Chemistry 中獲得。

Mastering Chemistry 更新的亮點

• 關鍵機制和機制概述影片以配對影片的形式創建。每個關鍵機制首先在概述影片中介紹，概述該機制的類型及理解所需的背景知識。然後，第二部影片引導學生通過該關鍵機制的代表性反應。

• 機制練習題提供一步提示，並在選定問題的任何步驟上預測產品功能，若學生遇到困難。這些問題為學生提供了一個通過練習學習的地方，並根據完成情況而非正確答案來獲得學分。

• 項目庫經過策劃、重新分類，並組織成四個層級，以幫助教師在 Mastering Chemistry 中導航資源。

• 第一層級包括完成即可獲得學分的練習題。

• 第二層級包括預測產品和單步機制。

• 第三層級包括新的多步機制，提供提示和多步問題，並標示框數和/或中間體。

• 第四層級包括合成問題。

• 隨時可用的學習工具可供學生自行使用，即使教授未指派模組。這些包括影片、練習測驗、練習考試和範例題。

本書特色

• 問題解決策略幫助學生將眾多複雜問題分解為更簡單的部分，並建立思考方法來處理複雜問題。策略涵蓋共振、酸鹼平衡和多步合成。

• 超過100道問題包括合成問題和基於近期文獻的問題。

幫助學生看到有機化學的相關性

• 在許多情況下強調綠色化學，介紹較少毒性、環保的試劑，例如用漂白劑而非鉻試劑氧化醇。

• 章節開頭專注於章節中討論的應用，並提供現代化的介紹和圖片。

• 章節中的應用框展示有機化學與學生生活和興趣領域的相關性，包括當代主題如生物化學、藥物、環境、醫學、燃料、綠色化學和綠色生活。

強調有機反應和機制

• 反應星爆在每個基於反應的章節的章節結尾之前出現，幫助學生更好地理解和心理組織反應的相似性和區別。

• 有機反應的視覺指南將主要章節中涵蓋的反應置於課程中所涵蓋的反應的整體背景中。

• 20個關鍵機制框突顯了在整個課程中反覆出現的基本機制原則，並且是一些較長、更複雜機制的基礎。每個框詳細描述反應的步驟，並提供具體範例以加強機制，並附上結尾問題以幫助學生吸收這些基本反應。

• 超過50個機制框幫助學生理解特定反應是如何發生的，通過詳細放大每個單獨步驟。

作者簡介

L.G. Skip Wade After receiving his B.A. from Ricein 1969, Wade went on to Harvard University, where he did research withProfessor James D. White. While at Harvard, he served as the Head TeachingFellow for the organic laboratories and was strongly influenced by the teachingmethods of two master educators, Professors Leonard K. Nash and Frank

H.Westheimer. After completing his Ph.D. at Harvard in 1974, Dr. Wade joined thechemistry faculty at Colorado State University. Over the course of fifteenyears at Colorado State, Dr. Wade taught organic chemistry to thousands ofstudents working toward careers in all areas of biology, chemistry, humanmedicine, veterinary medicine, and environmental studies. He also authoredresearch papers in organic synthesis and in chemical education, as well as elevenbooks reviewing current research in organic synthesis. Since 1989, Dr. Wade hasbeen a chemistry professor at Whitman College, where he teaches organicchemistry and pursues interests in organic synthesis and forensic chemistry.Dr. Wade received the A.E. Lange Award for Distinguished Science Teaching atWhitman in 1993.

Jan Simek was born to humble coal-miningparents who taught him to appreciate the importance of carbon at a very earlyage. At age 14, he was inspired to pursue a career teaching chemistry by hishigh school chemistry teacher, Joe Plaskas. Under the guidance of ProfessorKurt Kaufman at Kalamazoo College, Dr. Simek began lab work in synthesis ofnatural products that turned into research in hop extracts for the KalamazooSpice Extraction Company. After receiving a masters degree from StanfordUniversity, Dr. Simek worked in the pharmaceutical industry, synthesizingcompounds designed to control diabetes and atherosclerosis, and assisted in theisolation of anti-cancer antibiotics from natural sources. Returning toStanford University, Dr. Simek completed his Ph.D. with the legendary ProfessorCarl Djerassi, who developed the first synthesis of steroidal oralcontraceptives.

作者簡介(中文翻譯)

L.G. Skip Wade 在1969年從萊斯大學獲得學士學位後，前往哈佛大學，與詹姆斯·D·懷特教授進行研究。在哈佛期間，他擔任有機實驗室的首席教學助理，並受到兩位大師級教育者，萊昂納德·K·納什教授和法蘭克·H·韋斯特海默教授的教學方法深刻影響。

H. Westheimer 在1974年於哈佛大學完成博士學位後，韋德博士加入科羅拉多州立大學的化學系。在科羅拉多州立大學的十五年中，韋德博士教授有機化學，培養了數千名學生，這些學生在生物學、化學、人類醫學、獸醫學和環境研究等各個領域追求職業。他還撰寫了有關有機合成和化學教育的研究論文，以及十一本回顧當前有機合成研究的書籍。自1989年以來，韋德博士一直是惠特曼學院的化學教授，教授有機化學，並追求有機合成和法醫化學的興趣。韋德博士於1993年獲得惠特曼大學的A.E. Lange傑出科學教學獎。

Jan Simek 出生於一個謙遜的煤礦工人家庭，父母教導他在很小的年紀就懂得碳的重要性。在14歲時，他受到高中化學老師喬·普拉斯卡斯的啟發，決定追求化學教學的職業。在卡拉馬祖學院的庫爾特·考夫曼教授指導下，西梅克博士開始進行天然產物合成的實驗室工作，並轉向為卡拉馬祖香料提取公司研究啤酒花提取物。在斯坦福大學獲得碩士學位後，西梅克博士在製藥行業工作，合成旨在控制糖尿病和動脈硬化的化合物，並協助從天然來源分離抗癌抗生素。回到斯坦福大學後，西梅克博士在傳奇教授卡爾·傑拉西的指導下完成了博士學位，卡爾·傑拉西開發了第一個類固醇口服避孕藥的合成方法。

目錄大綱

1. Structure and Bonding
2. Acids and Bases: Functional Groups
3. Structure and Stereochemistry of Alkanes
4. The Study of Chemical Reactions
5. Stereochemistry
6. Alkyl Halides. Nucleophilic Substitution
7. Structure and Synthesis of Alkenes; Elimination
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 Thioethers
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
Answers to Selected Problems

目錄大綱(中文翻譯)

1. Structure and Bonding

2. Acids and Bases: Functional Groups

3. Structure and Stereochemistry of Alkanes

4. The Study of Chemical Reactions

5. Stereochemistry

6. Alkyl Halides. Nucleophilic Substitution

7. Structure and Synthesis of Alkenes; Elimination

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 Thioethers

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

Answers to Selected Problems

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