TEST BANK for Organic Chemistry 6th Edition
kkgh kkgh kkgh kkgh kkgh kkgh
kkgh Smith / All Chapters 1 - 29 / Full Complete
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Page
1
,Chapter 1 Structure and Bonding
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Chapter 2 Acids and Bases
kkgh kkgh kkgh kkgh
Chapter 3 Introduction to Organic Molecules and Functional Groups
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
Chapter 4 Alkanes
kkgh kkgh
Chapter 5 Stereochemistry
kkgh kkgh
Chapter 6 Understanding Organic Reactions
kkgh kkgh kkgh kkgh
Chapter 7 Alkyl Halides and Nucleophilic Substitution
kkgh kkgh kkgh kkgh kkgh kkgh
Chapter 8 Alkyl Halides and Elimination Reactions
kkgh kkgh kkgh kkgh kkgh kkgh
Chapter 9 Alcohols, Ethers, and Related Compounds
kkgh kkgh kkgh kkgh kkgh kkgh
Chapter 10 Alkenes and Addition Reactions
kkgh kkgh kkgh kkgh kkgh
Chapter 11 Alkynes and Synthesis
kkgh kkgh kkgh kkgh
Chapter 12 Oxidation and Reduction
kkgh kkgh kkgh kkgh
Spectroscopy A Mass Spectrometry
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Spectroscopy B Infrared Spectroscopy
kkgh kkgh kkgh
Spectroscopy C Nuclear Magnetic Resonance Spectroscopy
kkgh kkgh kkgh kkgh kkgh
Chapter 13 Radical Reactions
kkgh kkgh kkgh
Chapter 14 Conjugation, Resonance, and Dienes
kkgh kkgh kkgh kkgh kkgh
Chapter 15 Benzene and Aromatic Compounds
kkgh kkgh kkgh kkgh kkgh
Chapter 16 Reactions of Aromatic Compounds
kkgh kkgh kkgh kkgh kkgh
Chapter 17 Introduction to Carbonyl Chemistry: Organometallic
kkgh kkgh kkgh kkgh kkgh kkgh
Reagents; Oxidation and Reduction
kkgh kkgh kkgh kkgh
Chapter 18 Aldehydes and Ketones—Nucleophilic Addition
kkgh kkgh kkgh kkgh kkgh
Chapter 19 Carboxylic Acids and Nitriles
kkgh kkgh kkgh kkgh kkgh
Chapter 20 Carboxylic Acids and Their Derivatives- Nucleophilic Acyl
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
Substitution
kkgh
Chapter 21 Substitution Reactions of Carbonyl Compounds at the α-
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
Carbon
Chapter 22
kkgh Carbonyl Condensation Reactions
kkgh kkgh kkgh
Chapter 23
kkgh Amines
kkgh
Chapter 24
kkgh Carbon-Carbon Bond-Forming Reactions in Organic Synthesis
kkgh kkgh kkgh kkgh kkgh kkgh
Chapter 25
kkgh Pericyclic Reactions
kkgh kkgh
Chapter 26
kkgh Carbohydrates
kkgh
Chapter 27
kkgh Amino Acids and Proteins
kkgh kkgh kkgh kkgh
Chapter 28
kkgh Synthetic Polymers
kkgh kkgh
Chapter 29
kkgh Lipids (Available online)
kkgh kkgh kkgh
Page
2
,Page
3
, Chapter 1: Structure and Bonding kkgh kkgh kkgh kkgh
1. What is the ground-state electronic configuration of a carbon
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
atom? A)
kkgh 1s2, 2s2, 2p5
kkgh B) 1s2, 2s2, 2p2 C)
k k g h 1s2, kkgh kkgh k k g h kkgh kkgh k k g h
2s2, 2p6
kkgh kkgh D) 1s2, 2s2, 2p4 k k g h kkgh kkgh
2. What is the ground-state electronic configuration of a
kkgh kkgh kkgh kkgh kkgh kkgh kkgh
fluorine atom?A)
kkgh 1s2, 2s2, 2p2
kkgh B) 1s2, 2s2,
h
kg k k g h kkgh kkgh k k g h kkgh
3 2 2 4
2p
kkgh C) 1s , 2s , 2p D) 1s2, 2s2, k k g h kkgh kkgh k k g h kkgh
2p5
kkgh
3. What is the ground-state electronic configuration of a magnesium cation
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
(Mg2+)?A)
kkgh h
kg 1s2, 2s2, 2p6 C) 1s2, kkgh kkgh
2s2, 2p6, 3s2
kkgh kkgh kkgh
B) 1s2, 2s2, 2p6, 3s1 kkgh kkgh kkgh D) 1s2, 2s2, 2p6, 3s2, 3p2kkgh kkgh kkgh kkgh
4. What is the ground-state electronic configuration of a chlorine anion
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
(Cl—)?A)
kkgh h
kg 1s2, 2s2, 2p6 C) kkgh kkgh
2 2 6 2 5
1s , 2s , 2p , 3s , 3p
kkgh kkgh kkgh kkgh
B) 1s2, 2s2, 2p6, 3s2, 3p6
kkgh kkgh kkgh kkgh D) 1s2, 2s2, 2p6, 3s2, 3p4kkgh kkgh kkgh kkgh
5. Which of the following statements about valence electrons is true?
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
A) They are the most tightly held electrons.
kkgh kkgh kkgh kkgh kkgh kkgh
B) They do not participate in chemical reactions.
kkgh kkgh kkgh kkgh kkgh kkgh
Page
4
kkgh kkgh kkgh kkgh kkgh kkgh
kkgh Smith / All Chapters 1 - 29 / Full Complete
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
Page
1
,Chapter 1 Structure and Bonding
kkgh kkgh kkgh kkgh
Chapter 2 Acids and Bases
kkgh kkgh kkgh kkgh
Chapter 3 Introduction to Organic Molecules and Functional Groups
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
Chapter 4 Alkanes
kkgh kkgh
Chapter 5 Stereochemistry
kkgh kkgh
Chapter 6 Understanding Organic Reactions
kkgh kkgh kkgh kkgh
Chapter 7 Alkyl Halides and Nucleophilic Substitution
kkgh kkgh kkgh kkgh kkgh kkgh
Chapter 8 Alkyl Halides and Elimination Reactions
kkgh kkgh kkgh kkgh kkgh kkgh
Chapter 9 Alcohols, Ethers, and Related Compounds
kkgh kkgh kkgh kkgh kkgh kkgh
Chapter 10 Alkenes and Addition Reactions
kkgh kkgh kkgh kkgh kkgh
Chapter 11 Alkynes and Synthesis
kkgh kkgh kkgh kkgh
Chapter 12 Oxidation and Reduction
kkgh kkgh kkgh kkgh
Spectroscopy A Mass Spectrometry
kkgh kkgh kkgh
Spectroscopy B Infrared Spectroscopy
kkgh kkgh kkgh
Spectroscopy C Nuclear Magnetic Resonance Spectroscopy
kkgh kkgh kkgh kkgh kkgh
Chapter 13 Radical Reactions
kkgh kkgh kkgh
Chapter 14 Conjugation, Resonance, and Dienes
kkgh kkgh kkgh kkgh kkgh
Chapter 15 Benzene and Aromatic Compounds
kkgh kkgh kkgh kkgh kkgh
Chapter 16 Reactions of Aromatic Compounds
kkgh kkgh kkgh kkgh kkgh
Chapter 17 Introduction to Carbonyl Chemistry: Organometallic
kkgh kkgh kkgh kkgh kkgh kkgh
Reagents; Oxidation and Reduction
kkgh kkgh kkgh kkgh
Chapter 18 Aldehydes and Ketones—Nucleophilic Addition
kkgh kkgh kkgh kkgh kkgh
Chapter 19 Carboxylic Acids and Nitriles
kkgh kkgh kkgh kkgh kkgh
Chapter 20 Carboxylic Acids and Their Derivatives- Nucleophilic Acyl
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
Substitution
kkgh
Chapter 21 Substitution Reactions of Carbonyl Compounds at the α-
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
Carbon
Chapter 22
kkgh Carbonyl Condensation Reactions
kkgh kkgh kkgh
Chapter 23
kkgh Amines
kkgh
Chapter 24
kkgh Carbon-Carbon Bond-Forming Reactions in Organic Synthesis
kkgh kkgh kkgh kkgh kkgh kkgh
Chapter 25
kkgh Pericyclic Reactions
kkgh kkgh
Chapter 26
kkgh Carbohydrates
kkgh
Chapter 27
kkgh Amino Acids and Proteins
kkgh kkgh kkgh kkgh
Chapter 28
kkgh Synthetic Polymers
kkgh kkgh
Chapter 29
kkgh Lipids (Available online)
kkgh kkgh kkgh
Page
2
,Page
3
, Chapter 1: Structure and Bonding kkgh kkgh kkgh kkgh
1. What is the ground-state electronic configuration of a carbon
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
atom? A)
kkgh 1s2, 2s2, 2p5
kkgh B) 1s2, 2s2, 2p2 C)
k k g h 1s2, kkgh kkgh k k g h kkgh kkgh k k g h
2s2, 2p6
kkgh kkgh D) 1s2, 2s2, 2p4 k k g h kkgh kkgh
2. What is the ground-state electronic configuration of a
kkgh kkgh kkgh kkgh kkgh kkgh kkgh
fluorine atom?A)
kkgh 1s2, 2s2, 2p2
kkgh B) 1s2, 2s2,
h
kg k k g h kkgh kkgh k k g h kkgh
3 2 2 4
2p
kkgh C) 1s , 2s , 2p D) 1s2, 2s2, k k g h kkgh kkgh k k g h kkgh
2p5
kkgh
3. What is the ground-state electronic configuration of a magnesium cation
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
(Mg2+)?A)
kkgh h
kg 1s2, 2s2, 2p6 C) 1s2, kkgh kkgh
2s2, 2p6, 3s2
kkgh kkgh kkgh
B) 1s2, 2s2, 2p6, 3s1 kkgh kkgh kkgh D) 1s2, 2s2, 2p6, 3s2, 3p2kkgh kkgh kkgh kkgh
4. What is the ground-state electronic configuration of a chlorine anion
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
(Cl—)?A)
kkgh h
kg 1s2, 2s2, 2p6 C) kkgh kkgh
2 2 6 2 5
1s , 2s , 2p , 3s , 3p
kkgh kkgh kkgh kkgh
B) 1s2, 2s2, 2p6, 3s2, 3p6
kkgh kkgh kkgh kkgh D) 1s2, 2s2, 2p6, 3s2, 3p4kkgh kkgh kkgh kkgh
5. Which of the following statements about valence electrons is true?
kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh kkgh
A) They are the most tightly held electrons.
kkgh kkgh kkgh kkgh kkgh kkgh
B) They do not participate in chemical reactions.
kkgh kkgh kkgh kkgh kkgh kkgh
Page
4
