Organic Chemistry

Organic Chemistry

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About our author

After graduating from the Girls’ Latin School in Boston, Paula Bruice earned an A.B. from Mount Holyoke College and a Ph.D. in chemistry from the University of Virginia. She then received an NIH postdoctoral fellowship for study in the Department of Biochemistry at the University of Virginia Medical School and held a postdoctoral appointment in the Department of Pharmacology at Yale Medical School. Paula has been a member of the faculty at the University of California, Santa Barbara since 1972, where she has received the Associated Students Teacher of the Year Award, the Academic Senate Distinguished Teaching Award, two Mortar Board Professor of the Year Awards, and the UCSB Alumni Association Teaching Award.

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  • A print text
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For courses in Organic Chemistry (2-Semester)

 

A framework for organic chemistry built around the similarities in reaction types 

Paula Bruice’s presentation in Organic Chemistry, Eighth Edition provides mixed-science majors with the conceptual foundations, chemical logic, and problem-solving skills they need to reason their way to solutions for diverse problems in synthetic organic chemistry, biochemistry, and medicine. The Eighth Edition builds a strong framework for thinking about organic chemistry by unifying principles of reactivity that students will apply throughout the course, discouraging memorization. With more applications than any other textbook, Dr. Bruice consistently relates structure and reactivity to what occurs in our own cells and reinforces the fundamental reason for all chemical reactions–electrophiles react with nucleophiles. New streamlined coverage of substitution and elimination, updated problem-solving strategies, synthesis skill-building applications and tutorials guide students throughout fundamental and complex content in both the first and second semesters of the course.

Also available as a Pearson eText or packaged with Mastering Chemistry

 

Pearson eText is a simple-to-use, mobile-optimized, personalized reading experience that can be adopted on its own as the main course material. It lets students highlight, take notes, and review key vocabulary all in one place, even when offline. Seamlessly integrated videos and other rich media engage students and give them access to the help they need, when they need it. Educators can easily share their own notes with students so they see the connection between their eText and what they learn in class — motivating them to keep reading, and keep learning. Learn more about Pearson eText.

 

MasteringChemistry is an online homework, tutorial, and assessment system, designed to improve results by engaging students before, during, and after class with powerful content. Instructors ensure students arrive ready to learn by assigning educationally effective content before class, and encourage critical thinking and retention with in-class resources such as Learning Catalytics . Students can further master concepts after class through traditional and adaptive homework assignments that provide hints and answer-specific feedback. The Mastering gradebook records scores for all automatically graded assignments in one place, while diagnostic tools give instructors access to rich data to assess student understanding and misconceptions.

 

PART 1: AN INTRODUCTION TO THE STUDY OF ORGANIC CHEMISTRY

  • 1. Remembering General Chemistry: Electronic Structure and Bonding
  • 2. Acids and Bases: Central to Understanding Organic Chemistry
  • TUTORIAL: Acids and Bases
  • 3. An Introduction to Organic Compounds: Nomenclature, Physical Properties, and Structure

PART 2: ELECTROPHILIC ADDITION REACTIONS, STEREOCHEMISTRY, AND ELECTRON DELOCALIZATION

  • TUTORIAL: Using Molecular Models
  • 4. Isomers: The Arrangement of Atoms in Space
  • TUTORIAL: Interconverting Structural Representations
  • 5. Alkenes: Structure, Nomenclature, and an Introduction to Reactivity • Thermodynamics and Kinetics
  • TUTORIAL: Drawing Curved Arrows
  • 6. The Reactions of Alkenes • The Stereochemistry of Addition Reactions
  • 7. The Reactions of Alkynes • An Introduction to Multistep Synthesis
  • 8. Delocalized Electrons: Their Effect on Stability, pKa, and the Products of a Reaction • Aromaticity and Electronic Effects: An Introduction the Reactions of Benzene
  • TUTORIAL: Drawing Resonance Contributors

PART 3: SUBSTITUTION AND ELIMINATION REACTIONS

  • 9. Substitution and Elimination Reactions of Alkyl Halides
  • 10. Reactions of Alcohols, Ethers, Epoxides, Amines, and Sulfur-Containing Compounds
  • 11. Organometallic Compounds
  • 12. Radicals
  • TUTORIAL: Drawing Curved Arrows in Radical Systems

PART 4: IDENTIFICATION OF ORGANIC COMPOUNDS

  • 13. Mass Spectrometry; Infrared Spectroscopy; and UV/Vis Spectroscopy
  • 14. NMR Spectroscopy

PART 5: CARBONYL COMPOUNDS

  • 15. Reactions of Carboxylic Acids and Carboxylic Acid Derivatives
  • 16. Reactions of Aldehydes and Ketones • More Reactions of Carboxylic Acid Derivatives
  • 17. Reactions at the α-Carbon
  • TUTORIAL: Synthesis and Retrosynthetic Analysis

PART 6: AROMATIC COMPOUNDS

  • 18. Reactions of Benzene And Substituted Benzenes
  • 19. More About Amines • Reactions of Heterocyclic Compounds

PART 7: BIOORGANIC COMPOUNDS

  • 20. The Organic Chemistry Of Carbohydrates
  • 21. Amino Acids, Peptides, and Proteins
  • 22. Catalysis in Organic Reactions and in Enzymatic Reactions
  • 23. The Organic Chemistry of the Coenzymes, Compounds Derived from Vitamins
  • 24. The Organic Chemistry of the Metabolic Pathways
  • 25. The Organic Chemistry of Lipids
  • 26. The Chemistry of the Nucleic Acids

PART 8: SPECIAL TOPICS IN ORGANIC CHEMISTRY

  • 27. Synthetic Polymers
  • 28. Pericyclic Reactions

Appendices

  • I. pKa Values
  • II. Kinetics
  • III. Summary of Methods Used to Synthesize a Particular Functional Group
  • IV. Summary of Methods Employed to Form Carbon-Carbon Bonds
  • V. Spectroscopy Tables
  • VI. Physical Properties of Organic Compounds
  • VII. Answers to Selected Problems

Hallmark features of this title

  • Synthetic and retrosynthetic chemistry are introduced early, allowing students to grasp multistep synthesis from the beginning.
  • Problem Sets and Reaction Summaries at the end of chapters review key topics and reinforce essential skills.
  • Learn the Strategy labels guide students on how to approach various problems and develop critical-thinking skills.
  • Reactions of Organic Compounds Table organizes the reactions of organic compounds into 4 groups for similar chemical behavior to emphasize key characteristics and to build knowledge of the groups.
  • MCAT learning outcomes and MCAT-style questions in the Student’s Study Guide and Solutions Manual help prepare students for the MCAT exam.

For courses in Organic Chemistry (2-Semester)

 

Paula Bruice’s presentation in Organic Chemistry, Eighth Edition provides mixed-science majors with the conceptual foundations, chemical logic, and problem-solving skills they need to reason their way to solutions for diverse problems in synthetic organic chemistry, biochemistry, and medicine. The Eighth Edition builds a strong framework for thinking about organic chemistry by unifying principles of reactivity that students will apply throughout the course, discouraging memorization. With more applications than any other textbook, Dr. Bruice consistently relates structure and reactivity to what occurs in our own cells and reinforces the fundamental reason for all chemical reactions–electrophiles react with nucleophiles. New streamlined coverage of substitution and elimination, updated problem-solving strategies, synthesis skill-building applications and tutorials guide students throughout fundamental and complex content in both the first and second semesters of the course.

 

Also available as a Pearson eText or packaged with Mastering Chemistry

 

Pearson eText is a simple-to-use, mobile-optimized, personalized reading experience that can be adopted on its own as the main course material. It lets students highlight, take notes, and review key vocabulary all in one place, even when offline. Seamlessly integrated videos and other rich media engage students and give them access to the help they need, when they need it. Educators can easily share their own notes with students so they see the connection between their eText and what they learn in class – motivating them to keep reading, and keep learning.

 

Mastering combines trusted author content with digital tools and a flexible platform to personalize the learning experience and improve results for each student.Built for, and directly tied to the text, Mastering Chemistry enables an extension of learning, allowing students a platform to practice, learn, and apply outside of the classroom.

 

Note: You are purchasing a standalone book; Pearson eText and Mastering Chemistry do not come packaged with this content. Students, ask your instructor for the correct package ISBN and Course ID. Instructors, contact your Pearson representative for more information.

 

If your instructor has assigned Pearson eText as your main course material, search for:

• 0135213703 / 9780135213704 Pearson eText Organic Chemistry, 8/e — Access Card    

OR
• 0135213711 / 9780135213711 Pearson eText Organic Chemistry, 8/e — Instant Access

 

If your instructor has assigned Mastering Chemistry for your course, search for:

0134048148/9780134048147 Organic Chemistry Plus MasteringChemistry with eText — Access Card Package, 8/e

Package consists of:

  • 0134074661 / 9780134074665     MasteringChemistry with Pearson eText — ValuePack Access Card — for Organic Chemistry, 8/e
  • 013404228X / 9780134042282     Organic Chemistry, 8/e

 

New and updated features of this title

  • Marginal notes highlight relative reactivity and the Organizing What We Know feature now align with each other to better relate skill building to conceptual understanding.
  • Expanded annotations reinforce the revised art program and focus students on the most important material.
  • NEW & UPDATED: Applications boxes connect discussions to Medical, Environmental, Biological, Pharmaceutical, Nutritional, Chemical, Industrial, Historical and General applications in relating content to real life and future careers.
  • UPDATED: Tutorial spreads and Design a Synthesis sections explicitly highlight essential skills.

Additional information

Dimensions 2.00 × 9.70 × 10.60 in
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ISBN-13

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Subjects

science, chemistry, higher education, Physical Sciences, Organic Chemistry Two Semester