Organic Chemistry 4th edition

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Janice Gorzynski Smith
Publisher: McGraw-Hill Education

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  • 0: Tutorials and Templates (15)
  • 1: Structure and Bonding (12)
  • 2: Acids and Bases (15)
  • 3: Introduction to Organic Molecules and Functional Groups (16)
  • 4: Alkanes (31)
  • 5: Stereochemistry (19)
  • 6: Understanding Organic Reactions (19)
  • 7: Alkyl Halides and Nucleophilic Substitution (37)
  • 8: Alkyl Halides and Elimination Reactions (14)
  • 9: Alcohols, Ethers, and Epoxides (18)
  • 10: Alkenes (26)
  • 11: Alkynes (13)
  • 12: Oxidation and Reduction (1)
  • 13: Mass Spectrometry and Infrared Spectroscopy (13)
  • 14: Nuclear Magnetic Resonance Spectroscopy (13)
  • 15: Radical Reactions (6)
  • 16: Conjugation, Resonance, and Dienes (16)
  • 17: Benzene and Aromatic Compounds (10)
  • 18: Reactions of Aromatic Compounds (36)
  • 19: Carboxylic Acids and the Acidity of the O-H Bond (12)
  • 20: Introduction to Carbonyl Chemistry; Organometallic Reagents; Oxidation and Reduction (38)
  • 21: Aldehydes and Ketones—Nucleophilic Addition (16)
  • 22: Carboxylic Acids and Their Derivatives—Nucleophilic Acyl Substitution (19)
  • 23: Substitution Reactions of Carbonyl Compounds at the α Carbon (15)
  • 24: Carbonyl Condensation Reactions (12)
  • 25: Amines (30)
  • 26: Carbon-Carbon Bond-Forming Reactions in Organic Synthesis (6)
  • 27: Pericyclic Reactions (12)
  • 28: Carbohydrates (12)
  • 29: Amino Acids and Proteins (20)
  • 30: Lipids (14)
  • 31: Synthetic Polymers (8)

The WebAssign questions for this textbook are from a collection of questions developed by Dr. Kay Sandberg, an award winning organic chemistry instructor at North Carolina State University. These questions, covering the main topics in organic chemistry, have been correlated as closely as possible to the appropriate chapters in this textbook. This independent question collection provides a more secure solution to online homework for organic chemistry, since most organic chemistry textbook questions have detailed solutions published in the accompanying student solution guide. However, because these questions were not originally written for this textbook, it is recommended that you check each assigned problem to see if the material required for completing the question has been covered in your class. The question set has been extensively class-tested in large enrollment 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
P - Problems


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
1.P 12 001 002 003 004 005 006 007 008 009 010 011 012
Chapter 2: Acids and Bases
2.P 15 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015
Chapter 3: Introduction to Organic Molecules and Functional Groups
3.P 16 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016
Chapter 4: Alkanes
4.P 31 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016 017 018 019 020 021 022 023 024 025 026 027 028 029 030 031
Chapter 5: Stereochemistry
5.P 19 001 002 003 004 005 006 006.alt 007 008 009 010 011 012 013 014 015 016 017 018
Chapter 6: Understanding Organic Reactions
6.P 19 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016 017 018 018.alt
Chapter 7: Alkyl Halides and Nucleophilic Substitution
7.P 37 001 002 003 003.alt 004 004.alt 005 005.alt 006 007 008 009 010 010.alt 011 012 013 014 015 016 016.alt 017 018 019 020 021 022 023 024 025 026 027 028 029 030 031 031.alt
Chapter 8: Alkyl Halides and Elimination Reactions
8.P 14 001 002 003 004 005 006 007 008 009 009.alt 010 011 012 013
Chapter 9: Alcohols, Ethers, and Epoxides
9.P 18 001 002 003 004 005 006 007 008 009 010 011 012 013.alt 014 015 016 017 018
Chapter 10: Alkenes
10.P 26 001 002 003 004 005 006 007 008 009 010 011 012 012.alt 013 014 015 016 017 018 019 020 021 022 023 024 025
Chapter 11: Alkynes
11.P 13 001 002 003 004 005 006 007 008 009 010 011 012 013
Chapter 12: Oxidation and Reduction
12.P 1 001
Chapter 13: Mass Spectrometry and Infrared Spectroscopy
13.P 13 001 002 003 004 005 006 007 008 009 010 011 012 013
Chapter 14: Nuclear Magnetic Resonance Spectroscopy
14.P 13 001 002 003 004 005 006 007 008 009 010 011 012 013
Chapter 15: Radical Reactions
15.P 6 001 002 003 004 005 006
Chapter 16: Conjugation, Resonance, and Dienes
16.P 16 001 002 003 004 005 006 007 008 009 010 011 012 012.alt 013 014 015
Chapter 17: Benzene and Aromatic Compounds
17.P 10 001 002 003 004 005 006 007 008 009 010
Chapter 18: Reactions of Aromatic Compounds
18.P 36 001 002 003 004 005 006 007 008 009 010 011 012 013 013.alt 014 015 016 017 018 019 020 020.alt 021 022 022.alt 023 024 025 026 027 028 029 030 031 032 033
Chapter 19: Carboxylic Acids and the Acidity of the O-H Bond
19.P 12 001 002 003 004 005 005.alt 006 007 008 009 010 011
Chapter 20: Introduction to Carbonyl Chemistry; Organometallic Reagents; Oxidation and Reduction
20.P 38 001 002 003 004 004.alt 005 006 007 008 009 010 011 012 013 014 014.alt 015 016 017 018 019 020 021 022 023 024 025 026 027 028 028.alt 029 030 031 032 033 034 035
Chapter 21: Aldehydes and Ketones—Nucleophilic Addition
21.P 16 001 002 003 004 005 005.alt 006 007 008 009 010 011 012 013 014 015
Chapter 22: Carboxylic Acids and Their Derivatives—Nucleophilic Acyl Substitution
22.P 19 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015 016 017 018 019
Chapter 23: Substitution Reactions of Carbonyl Compounds at the α Carbon
23.P 15 001 002 003 004 005 006 007 008 009 010 011 012 013 014 015
Chapter 24: Carbonyl Condensation Reactions
24.P 12 001 002 003 004 005 006 007 008 009 010 011 012
Chapter 25: Amines
25.P 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
Chapter 26: Carbon-Carbon Bond-Forming Reactions in Organic Synthesis
26.P 6 001 002 003 004 005 006
Chapter 27: Pericyclic Reactions
27.P 12 001 002 003 004 005 006 007 008 009 009.alt 010 011
Chapter 28: Carbohydrates
28.P 12 001 002 003 004 005 006 007 008 009 010 011 012
Chapter 29: Amino Acids and Proteins
29.P 20 001 002 003 004 005 006 007 008 008.alt 009 010 011 012 013 014 015 016 017 018 019
Chapter 30: Lipids
30.P 14 001 002 003 003.alt 004 005 005.alt 006 007 008 009 010 011 012
Chapter 31: Synthetic Polymers
31.P 8 001 002 003 003.alt 004 005 005.alt 006
Total 544