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Test Bank — Organic Chemistry, 9th Edition — John E. McMurry — ISBN 9781305080485

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The Test Bank for Organic Chemistry, 9th Edition by John E. McMurry offers a fully verified suite of questions mapped precisely to the official Cengage edition. This resource includes multiple-choice, true/false, short-answer, and mechanism-based problems aligned with each chapter’s learning objectives, intended for quizzes, midterms, and final exams. All chapter titles below are verified from the official publisher’s Table of Contents and presented in continuous prose with bold formatting: Chapter 1: Structure and Bonding, Chapter 2: Polar Covalent Bonds; Acids and Bases, Chapter 3: Organic Compounds: Alkanes and Their Stereochemistry, Chapter 4: Organic Compounds: Cycloalkanes and Their Stereochemistry, Chapter 5: Stereochemistry at Tetrahedral Centers, Chapter 6: An Overview of Organic Reactions, Chapter 7: Alkenes: Structure and Reactivity, Chapter 8: Alkenes: Reactions and Synthesis, Chapter 9: Alkynes: An Introduction to Organic Synthesis, Chapter 10: Organohalides, Chapter 11: Reactions of Alkyl Halides: Nucleophilic Substitutions and Eliminations, Chapter 12: Structure Determination: Mass Spectrometry and Infrared Spectroscopy, Chapter 13: Structure Determination: Nuclear Magnetic Resonance Spectroscopy, Chapter 14: Conjugated Compounds and Ultraviolet Spectroscopy, Chapter 15: Benzene and Aromaticity, Chapter 16: Chemistry of Benzene: Electrophilic Aromatic Substitution, Chapter 17: Alcohols and Phenols, Chapter 18: Ethers and Epoxides; Thiols and Sulfides, Chapter 19: Aldehydes and Ketones: Nucleophilic Addition Reactions, Chapter 20: Carboxylic Acids and Nitriles, Chapter 21: Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions, Chapter 22: Carbonyl Alpha-Substitution Reactions, Chapter 23: Carbonyl Condensation Reactions, Chapter 24: Amines and Heterocycles, Chapter 25: Biomolecules: Carbohydrates, Chapter 26: Biomolecules: Amino Acids, Peptides, and Proteins, Chapter 27: Biomolecules: Lipids, Chapter 28: Biomolecules: Nucleic Acids, Chapter 29: The Organic Chemistry of Metabolic Pathways, Chapter 30: Orbitals and Organic Chemistry: Pericyclic Reactions, Chapter 31: Synthetic Polymers.

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Organic Chemistry – 9th Edition
ST

TEST BANK
UV
IA

John E. McMurry
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AP

Comprehensive Test Bank for Instructors
PR

and Students
OV

© John E. McMurry

All rights reserved. Reproduction or distribution without permission is prohibited.
ED
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Created by MedConnoisseur ©2025/2026

, TABLE OF CONTENTS
Organic Chemistry – 9th Edition
ST
John E. McMurry


1. Structure and Bonding
UV

2. Polar Covalent Bonds; Acids and Bases
3. Organic Compounds: Alkanes and Their Stereochemistry
4. Organic Compounds: Cycloalkanes and Their Stereochemistry
5. Stereochemistry at Tetrahedral Centers
6. An Overview of Organic Reactions
IA
7. Alkenes: Structure and Reactivity
8. Alkenes: Reactions and Synthesis
9. Alkynes: An Introduction to Organic Synthesis
10. Organohalides
?_

11. Reactions of Alkyl Halides: Nucleophilic Substitutions and Eliminations
12. Structure Determination: Mass Spectrometry and Infrared Spectroscopy
13. Structure Determination: Nuclear Magnetic Resonance Spectroscopy
14. Conjugated Compounds and Ultraviolet Spectroscopy
AP

15. Benzene and Aromaticity
16. Chemistry of Benzene: Electrophilic Aromatic Substitution
17. Alcohols and Phenols
18. Ethers and Epoxides; Thiols and Sulfides
19. Aldehydes and Ketones: Nucleophilic Addition Reactions
PR

20. Carboxylic Acids and Nitriles
21. Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions
22. Carbonyl Alpha-Substitution Reactions
23. Carbonyl Condensation Reactions
OV
24. Amines and Heterocycles
25. Biomolecules: Carbohydrates
26. Biomolecules: Amino Acids, Peptides, and Proteins
27. Biomolecules: Lipids
28. Biomolecules: Nucleic Acids
29. The Organic Chemistry of Metabolic Pathways
ED

30. Orbitals and Organic Chemistry: Pericyclic Reactions
31. Synthetic Polymers
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Created by MedConnoisseur ©2025/2026

, Chapter 01 - Structure and Bonding
1. Give the ground-state electron configuration for carbon (atomic number 6).
ANSWER: 1s22s22px12py1 or 1s22s22p2
POINTS: 1
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2. Give the ground-state electron configuration for fluorine (atomic number 9).
ANSWER: 1s22s22px2 2py2 2pz1 or 1s22s22p5
POINTS: 1
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3. Give the ground-state electron configuration for magnesium (atomic number 12).
ANSWER: 1s22s22p63s2
POINTS: 1

4. How many electrons does silicon have in its valence shell?
ANSWER: four
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POINTS: 1

Exhibit 1-1
Write valid Lewis (electron-dot) structures for each formula below. Show all electrons as dots and show all non-bonding
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electrons.

5. C2Cl4 tetrachloroethylene
ANSWER:
AP
POINTS: 1

6. CO2 carbon dioxide
PR
ANSWER:
POINTS: 1

7. CH4O methanol
ANSWER:
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POINTS: 1

Exhibit 1-2
Consider the structure of urea, shown below, to answer the following question(s).
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8. Refer to Exhibit 1-2. Fill in any non-bonding valence electrons that are missing from the line-bond structure.
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Cengage Learning Testing, Powered by Cognero Page 1

, Chapter 01 - Structure and Bonding
ANSWER:


POINTS: 1
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9. Refer to Exhibit 1-2. The carbon atom in urea is:
3
a. sp hybridized
2
b. sp hybridized
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c. sp hybridized
d. not hybridized
ANSWER: b
POINTS: 1

10. Refer to Exhibit 1-2. The predicted NH2−C=O bond angle in urea is:
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a. 109.5°
b. 120°
c. 180°
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d. not predictable
ANSWER: b
POINTS: 1

Exhibit 1-3
AP
Determine the hybridization for the indicated atoms in each structure below.
PR
11. Refer to Exhibit 1-3. The hybridization of this oxygen atom (A) is ______.
ANSWER: 2
sp
POINTS: 1
OV
12. Refer to Exhibit 1-3. The hybridization of this oxygen atom (B) is ______.
ANSWER: sp3
POINTS: 1

13. Refer to Exhibit 1-3. The hybridization of this carbon atom (C) is ______.
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ANSWER: sp3
POINTS: 1

14. Refer to Exhibit 1-3. The hybridization of this carbon atom (D) is ______.
ANSWER: sp
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POINTS: 1


Cengage Learning Testing, Powered by Cognero Page 2

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