Organic Chemistry: Structure and Function 7th edition

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K. Peter C. Vollhardt and Neil E. Schore
Publisher: W. H. Freeman

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  • 0: Tutorials and Templates (15)
  • 1: Structure and Bonding in Organic Molecules (30)
  • 2: Structure and Reactivity (55)
  • 3: Reactions of Alkanes (18)
  • 4: Cycloalkanes (32)
  • 5: Stereoisomers (29)
  • 6: Properties and Reactions of Haloalkanes (36)
  • 7: Further Reactions of Haloalkanes (62)
  • 8: Hydroxy Functional Group: Alcohols (42)
  • 9: Further Reactions of Alcohols and the Chemistry of Ethers (35)
  • 10: Using Nuclear Magnetic Resonance Spectroscopy to Deduce Structure (25)
  • 11: Alkenes: Infrared Spectroscopy and Mass Spectrometry (30)
  • 12: Reactions of Alkenes (60)
  • 13: Alkynes (23)
  • 14: Delocalized Pi Systems (29)
  • 15: Benzene and Aromaticity (26)
  • 16: Electrophilic Attack on Derivatives of Benzene (38)
  • 17: Aldehydes and Ketones (49)
  • 18: Enols, Enolates, and the Aldol Condensation (22)
  • 19: Carboxylic Acids (35)
  • 20: Carboxylic Acid Derivatives (51)
  • 21: Amines and Their Derivatives (42)
  • 22: Chemistry of Benzene Substituents (12)
  • 23: Ester Enolates and the Claisen Condensation (37)
  • 24: Carbohydrates (19)
  • 25: Heterocycles (15)
  • 26: Amino Acids, Peptides, Proteins, and Nucleic Acids (21)
Dr. Jerry Jenkins is the Chair of the Organic Chemistry and Biochemistry Department at Otterbein College. Dr. Jenkins is the author of the Organic Chemistry Workbook available from the W.H. Freeman publishing company. The 300 questions in the WebAssign version of this book are randomized versions of 659 questions selected from the more than 1,000 questions available in the print edition.

Dr. Kay Sandberg is an experienced Organic Chemistry instructor at North Carolina State University. Because it is customary in organic chemistry to publish a complete student solution guide for every end-of-chapter question, the student guide renders the textbook end-of-chapter questions unusable for an online homework system. Dr. Sandberg developed this set of 500 questions exclusively for WebAssign to address this problem. The questions cover the main topics in organic chemistry, and have been correlated as closely as possible to the appropriate chapter in the textbook. The question set has been extensively class-tested in multiple 200-student courses at NC State.

Question Collection Features: Questions requiring automatic assessment of student-drawn structures, including skeletal structures, Lewis structures, reaction mechanisms with electron-flow arrows ("pushing electrons"), isotopically-labeled reactions, and multi-step syntheses, use the popular MarvinSketch application. WebAssign grades these structures automatically, checking for stereo features, rings, chains, etc.

Questions requiring automatic assessment of chemical formulas and reaction equations use WebAssign's chemPad, an intuitive answer-entry palette with over 150 lines of intelligent answer feedback.

Other questions use a variety of response types, including fill-in-the-blank, multiple-choice, multiple-select and numerical entry.



Question Group Key
tutorial - Tutorials
template - Templates
S - Sandberg Problems
J - Jenkins Workbook
E - Exercises


Question Availability Color Key
BLACK questions are available now
GRAY questions are under development


Group Quantity Questions
Chapter 0: Tutorials and Templates
0.template 12 complete.mrv condensed.mrv lewis.mrv mechanism.mrv mechanism_adv.mrv multistep.mrv reaction.mrv reaction_adv.mrv resonance.mrv skeleton.mrv skeleton_adv.mrv splitarray.mrv
0.tutorial 3 lewis.structures marvinsketch.introduction multistep.mechanism
Chapter 1: Structure and Bonding in Organic Molecules
1.J 13 001 002 003 004 005 006 007 008 008.alt 009 010 011 013
1.S 17 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016 017
Chapter 2: Structure and Reactivity
2.J 16 001 001.alt 002 002.alt 003 003.alt 004 005 006 006.alt 007 008 009 010 011 012
2.S 39 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016 017 018 019 020 021 022 023 024 025 026 027 028 029 030 031 032 033 034 035 036 037 038 039
Chapter 3: Reactions of Alkanes
3.E 4 001 002 003 004
3.J 3 001 002 003
3.S 11 001 002 003 004 005 006 007 008 009 010 011
Chapter 4: Cycloalkanes
4.J 11 001 002 003 004 005 006 007 008 009 010 011
4.S 21 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016 017 018 019 020 021
Chapter 5: Stereoisomers
5.J 10 001 002 003 004 005 006 007 008 009 009b 010
5.S 19 001 002 003 004 005 006 006.alt 007 008 009 010 011 012 013 014 015 016 017 018
Chapter 6: Properties and Reactions of Haloalkanes
6.E 2 001 002
6.J 9 001 002 003 004 005 006 006.alt 007 008
6.S 25 001 002 003 004 005 006 006.alt 007 007.alt 008 008.alt 009 010 011 012 013 014 015 015.alt 016 017 018 019 020 021
Chapter 7: Further Reactions of Haloalkanes
7.J 15 001 002 003 004 005 006 007 008 009 010 011 012 013 013.alt 014
7.S 47 001 002 003 004 005 006 007 008 009 009.alt 010 011 012 013 014 015 016 017 017.alt 018 019 020 020.alt 021 022 023 024 025 026 027 028 029 030 031 032 033 034 035 036 037 038 039 040 041 042 043 044
Chapter 8: Hydroxy Functional Group: Alcohols
8.J 21 001 002 003 004 005 006 007 008 009 010 011 012 013 014 014.alt 015 015.alt 016 016.alt 017 017.alt
8.S 21 001 002 003 004 005 005.alt 006 007 008 009 010 011 012 013 014 015 016 017 018 019 020
Chapter 9: Further Reactions of Alcohols and the Chemistry of Ethers
9.J 15 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015
9.S 20 001 002 003 004.alt 005 006 007 008 009 010 011 011.alt 012 013 014 015 016 017 018 019
Chapter 10: Using Nuclear Magnetic Resonance Spectroscopy to Deduce Structure
10.J 10 001 002 003 004 005 006 007 008 009 010
10.S 15 001 001.alt 002 003 004 005 006 007 008 009 010 011 012 013 014
Chapter 11: Alkenes: Infrared Spectroscopy and Mass Spectrometry
11.J 5 001 002 003 004 005
11.S 25 001 002 003 004 005 006 007 008 009 009.alt 010 010.alt 011 012 013 014 015 016 017 018 019 020 021 022 023
Chapter 12: Reactions of Alkenes
12.J 29 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 015.alt 016 016.alt 017 017.alt 018 018.alt 019 019.alt 020 021 022 023 024
12.S 31 001 002 003 003.alt 004 005 006 007 008 009 010 011 012 013 014 015 016 017 018 019 019.alt 020 021 021.alt 022 023 024 025 026 027 027.alt
Chapter 13: Alkynes
13.J 8 001 002 003 004 005 006 007 008
13.S 15 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015
Chapter 14: Delocalized Pi Systems
14.J 7 001 002 003 004 005 006 007
14.S 22 001 002 003 004 005 006 007 008 009 010 011 012 012.alt 013 014 015 016 017 018 019 020 021
Chapter 15: Benzene and Aromaticity
15.E 5 001 002 003 004 005
15.J 9 001 002 003 004 005 006 007 008 009
15.S 12 001 002 003 004 005 006 007 008 009 010 011 012
Chapter 16: Electrophilic Attack on Derivatives of Benzene
16.J 14 001 002 003 004 005 006 007 008 009 010 011 011.alt 012 013
16.S 24 001 002 003 003.alt 004 005 006 007 008 009 009.alt 010 011 011.alt 012 013 014 015 016 017 018 019 020 021
Chapter 17: Aldehydes and Ketones
17.J 30 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016 017 018 019 020 021 022 023 024 025 026 027 028 029 030
17.S 19 001 002 003 004 005 006 007 008 008.alt 009 010 011 012 013 014 015 016 017 018
Chapter 18: Enols, Enolates, and the Aldol Condensation
18.J 16 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016
18.S 6 001 002 003 004 005 006
Chapter 19: Carboxylic Acids
19.J 17 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016 017
19.S 18 001 002 003 004 005 006 007 007.alt 008 009 010 011 012 013 014 015 016 017
Chapter 20: Carboxylic Acid Derivatives
20.J 25 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016 017 018 019 020 021 022 023 024 025
20.S 26 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016 017 018 019 020 021 022 023 024 024.alt 025
Chapter 21: Amines and Their Derivatives
21.E 8 001 002 003 004 005 006 007 008
21.J 13 001 002 003 004 005 006 007 008 009 010 011 012 013
21.S 21 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016 017 018 019 020 021
Chapter 22: Chemistry of Benzene Substituents
22.S 12 001 002 003 004 005 006 007 008 009 010 011 012
Chapter 23: Ester Enolates and the Claisen Condensation
23.J 19 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016 017 018 019
23.S 18 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016 017 018
Chapter 24: Carbohydrates
24.E 7 001 002 003 004 005 006 007
24.S 12 001 002 003 004 005 006 007 008 009 010 011 012
Chapter 25: Heterocycles
25.E 2 001 002
25.S 13 001 002 002.alt 003 004 005 006 007 008 009 010 011 012
Chapter 26: Amino Acids, Peptides, Proteins, and Nucleic Acids
26.S 21 001 002 003 004 005 006 007 008 009 009.alt 010 011 012 013 014 015 016 017 018 019 020
Total 888 (1)