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TEST BANK FOR Organic Chemistry 9th Edition by John McMurry , ISBN: 9781305080485 |Chapters 1-31, Appendices A-D| Guide A+

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TEST BANK FOR Organic Chemistry 9th Edition by John McMurry , ISBN: 9781305080485 |Chapters 1-31, Appendices A-D| Guide A+

Institution
Organic Chemistry
Course
Organic Chemistry

Content preview

TEST BANK
Organic Chemistry

John McMurry

9th Edition
PR
O
FD
O
C

,Table of Contents

1. Structure and Bonding
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
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
15. Benzene and Aromaticity
16. Chemistry of Benzene: Electrophilic Aromatic Substitution
PR
17. Alcohols and Phenols
18. Ethers and Epoxides; Thiols and Sulfides
19. Aldehydes and Ketones: Nucleophilic Addition Reactions
20. Carboxylic Acids and Nitriles
21. Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions
22. Carbonyl Alpha-Substitution Reactions
23. Carbonyl Condensation Reactions
O
24. Amines and Heterocycles
25. Biomolecules: Carbohydrates
26. Biomolecules: Amino Acids, Peptides, and Proteins
FD
27. Biomolecules: Lipids
28. Biomolecules: Nucleic Acids
29. The Organic Chemistry of Metabolic Pathways
30. Orbitals and Organic Chemistry: Pericyclic Reactions
31. Synthetic Polymers
O

Appendices
C
• Appendix A: Nomenclature of Polyfunctional Organic Compounds
• Appendix B: Acidity Constants for Some Organic Compounds
• Appendix C: Glossary
• Appendix D: Answers to In-Text Problems

,Chapter 01 - Structure and Bonding
1. Give the ground-state electron configuration for carbon (atomic number 6).
ANSWER: 1s22s22px12py1 or 1s22s22p2
POINTS: 1

2. Give the ground-state electron configuration for fluorine (atomic number 9).
ANSWER: 1s22s22px2 2py2 2pz1 or 1s22s22p5
POINTS: 1

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
PR
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
electrons.
O
5. C2Cl4 tetrachloroethylene
ANSWER:
FD

POINTS: 1

6. CO2 carbon dioxide
O
ANSWER:
POINTS: 1
C
7. CH4O methanol
ANSWER:



POINTS: 1

Exhibit 1-2
Consider the structure of urea, shown below, to answer the following question(s).




8. Refer to Exhibit 1-2. Fill in any non-bonding valence electrons that are missing from the line-bond structure.

, ANSWER:


POINTS: 1

9. Refer to Exhibit 1-2. The carbon atom in urea is:

a. sp3 hybridized
b. sp2 hybridized
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:
PR
a. 109.5°
b. 120°
c. 180°
d. not predictable
ANSWER: b
POINTS: 1
O

Exhibit 1-3
Determine the hybridization for the indicated atoms in each structure below.
FD
O
11. Refer to Exhibit 1-3. The hybridization of this oxygen atom (A) is .
ANSWER: sp2
C
POINTS: 1

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 .
ANSWER: sp3
POINTS: 1

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

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Institution
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Course
Organic Chemistry

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