Deck 8: Delocalized Electrons Their Eff

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Question
Which of the following is not acceptable when drawing resonance structures?

A) Move electrons to sp or sp2 hybridized atoms.
B) Positive charges are moved toward electrons.
C) Move lone-pair electrons.
D) Never move atoms.
E) Move pi electrons.
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Question
Which of the following is not an acceptable resonance structure of I?
<strong>Which of the following is not an acceptable resonance structure of I?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A) <strong>Which of the following is not an acceptable resonance structure of I?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which of the following is not an acceptable resonance structure of I?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which of the following is not an acceptable resonance structure of I?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which of the following is not an acceptable resonance structure of I?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which of the following is not an acceptable resonance structure of I?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which structure makes the largest contribution to the resonance hybrid?

A) <strong>Which structure makes the largest contribution to the resonance hybrid?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which structure makes the largest contribution to the resonance hybrid?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which structure makes the largest contribution to the resonance hybrid?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which structure makes the largest contribution to the resonance hybrid?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which structure makes the largest contribution to the resonance hybrid?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following is the strongest acid?

A) <strong>Which of the following is the strongest acid?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which of the following is the strongest acid?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which of the following is the strongest acid?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which of the following is the strongest acid?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which of the following is the strongest acid?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following products is the result of either 1,2 or 1,4-addition of HBr and is most stable? <strong>Which of the following products is the result of either 1,2 or 1,4-addition of HBr and is most stable?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A) <strong>Which of the following products is the result of either 1,2 or 1,4-addition of HBr and is most stable?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which of the following products is the result of either 1,2 or 1,4-addition of HBr and is most stable?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which of the following products is the result of either 1,2 or 1,4-addition of HBr and is most stable?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which of the following products is the result of either 1,2 or 1,4-addition of HBr and is most stable?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which of the following products is the result of either 1,2 or 1,4-addition of HBr and is most stable?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which diene will react most readily with a dienophile?

A) <strong>Which diene will react most readily with a dienophile?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which diene will react most readily with a dienophile?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which diene will react most readily with a dienophile?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which diene will react most readily with a dienophile?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which diene will react most readily with a dienophile?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which compound is the expected product of this reaction? <strong>Which compound is the expected product of this reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A) <strong>Which compound is the expected product of this reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which compound is the expected product of this reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which compound is the expected product of this reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which compound is the expected product of this reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which compound is the expected product of this reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following criteria must be met for a molecule to be aromatic?

A) The molecule must be cyclic.
B) The molecule must be planar.
C) Every atom must have a p orbital.
D) The molecule must contain an odd number of pairs of ? electrons.
E) All of the above.
Question
Which products are, respectively, the kinetic and thermodynamic product? <strong>Which products are, respectively, the kinetic and thermodynamic product?  </strong> A) 1,2 B) 1,3 C) 2,1 D) 2,3 E) 3,1 <div style=padding-top: 35px>

A) 1,2
B) 1,3
C) 2,1
D) 2,3
E) 3,1
Question
Assuming planarity, which of the following molecules is aromatic?

A) <strong>Assuming planarity, which of the following molecules is aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Assuming planarity, which of the following molecules is aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Assuming planarity, which of the following molecules is aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Assuming planarity, which of the following molecules is aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Assuming planarity, which of the following molecules is aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following molecular orbital diagrams
best fits that of pyrrole?
pyrrole
<strong>Which of the following molecular orbital diagrams best fits that of pyrrole? pyrrole  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>Which of the following molecular orbital diagrams best fits that of pyrrole? pyrrole  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Which of the following molecular orbital diagrams best fits that of pyrrole? pyrrole  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which of the following molecular orbital diagrams best fits that of pyrrole? pyrrole  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which of the following molecular orbital diagrams best fits that of pyrrole? pyrrole  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
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Deck 8: Delocalized Electrons Their Eff
1
Which of the following is not acceptable when drawing resonance structures?

A) Move electrons to sp or sp2 hybridized atoms.
B) Positive charges are moved toward electrons.
C) Move lone-pair electrons.
D) Never move atoms.
E) Move pi electrons.
Positive charges are moved toward electrons.
2
Which of the following is not an acceptable resonance structure of I?
<strong>Which of the following is not an acceptable resonance structure of I?  </strong> A)   B)   C)   D)   E)

A) <strong>Which of the following is not an acceptable resonance structure of I?  </strong> A)   B)   C)   D)   E)
B) <strong>Which of the following is not an acceptable resonance structure of I?  </strong> A)   B)   C)   D)   E)
C) <strong>Which of the following is not an acceptable resonance structure of I?  </strong> A)   B)   C)   D)   E)
D) <strong>Which of the following is not an acceptable resonance structure of I?  </strong> A)   B)   C)   D)   E)
E) <strong>Which of the following is not an acceptable resonance structure of I?  </strong> A)   B)   C)   D)   E)

3
Which structure makes the largest contribution to the resonance hybrid?

A) <strong>Which structure makes the largest contribution to the resonance hybrid?</strong> A)   B)   C)   D)   E)
B) <strong>Which structure makes the largest contribution to the resonance hybrid?</strong> A)   B)   C)   D)   E)
C) <strong>Which structure makes the largest contribution to the resonance hybrid?</strong> A)   B)   C)   D)   E)
D) <strong>Which structure makes the largest contribution to the resonance hybrid?</strong> A)   B)   C)   D)   E)
E) <strong>Which structure makes the largest contribution to the resonance hybrid?</strong> A)   B)   C)   D)   E)

4
Which of the following is the strongest acid?

A) <strong>Which of the following is the strongest acid?</strong> A)   B)   C)   D)   E)
B) <strong>Which of the following is the strongest acid?</strong> A)   B)   C)   D)   E)
C) <strong>Which of the following is the strongest acid?</strong> A)   B)   C)   D)   E)
D) <strong>Which of the following is the strongest acid?</strong> A)   B)   C)   D)   E)
E) <strong>Which of the following is the strongest acid?</strong> A)   B)   C)   D)   E)
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5
Which of the following products is the result of either 1,2 or 1,4-addition of HBr and is most stable? <strong>Which of the following products is the result of either 1,2 or 1,4-addition of HBr and is most stable?  </strong> A)   B)   C)   D)   E)

A) <strong>Which of the following products is the result of either 1,2 or 1,4-addition of HBr and is most stable?  </strong> A)   B)   C)   D)   E)
B) <strong>Which of the following products is the result of either 1,2 or 1,4-addition of HBr and is most stable?  </strong> A)   B)   C)   D)   E)
C) <strong>Which of the following products is the result of either 1,2 or 1,4-addition of HBr and is most stable?  </strong> A)   B)   C)   D)   E)
D) <strong>Which of the following products is the result of either 1,2 or 1,4-addition of HBr and is most stable?  </strong> A)   B)   C)   D)   E)
E) <strong>Which of the following products is the result of either 1,2 or 1,4-addition of HBr and is most stable?  </strong> A)   B)   C)   D)   E)
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6
Which diene will react most readily with a dienophile?

A) <strong>Which diene will react most readily with a dienophile?</strong> A)   B)   C)   D)   E)
B) <strong>Which diene will react most readily with a dienophile?</strong> A)   B)   C)   D)   E)
C) <strong>Which diene will react most readily with a dienophile?</strong> A)   B)   C)   D)   E)
D) <strong>Which diene will react most readily with a dienophile?</strong> A)   B)   C)   D)   E)
E) <strong>Which diene will react most readily with a dienophile?</strong> A)   B)   C)   D)   E)
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7
Which compound is the expected product of this reaction? <strong>Which compound is the expected product of this reaction?  </strong> A)   B)   C)   D)   E)

A) <strong>Which compound is the expected product of this reaction?  </strong> A)   B)   C)   D)   E)
B) <strong>Which compound is the expected product of this reaction?  </strong> A)   B)   C)   D)   E)
C) <strong>Which compound is the expected product of this reaction?  </strong> A)   B)   C)   D)   E)
D) <strong>Which compound is the expected product of this reaction?  </strong> A)   B)   C)   D)   E)
E) <strong>Which compound is the expected product of this reaction?  </strong> A)   B)   C)   D)   E)
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8
Which of the following criteria must be met for a molecule to be aromatic?

A) The molecule must be cyclic.
B) The molecule must be planar.
C) Every atom must have a p orbital.
D) The molecule must contain an odd number of pairs of ? electrons.
E) All of the above.
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9
Which products are, respectively, the kinetic and thermodynamic product? <strong>Which products are, respectively, the kinetic and thermodynamic product?  </strong> A) 1,2 B) 1,3 C) 2,1 D) 2,3 E) 3,1

A) 1,2
B) 1,3
C) 2,1
D) 2,3
E) 3,1
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10
Assuming planarity, which of the following molecules is aromatic?

A) <strong>Assuming planarity, which of the following molecules is aromatic?</strong> A)   B)   C)   D)   E)
B) <strong>Assuming planarity, which of the following molecules is aromatic?</strong> A)   B)   C)   D)   E)
C) <strong>Assuming planarity, which of the following molecules is aromatic?</strong> A)   B)   C)   D)   E)
D) <strong>Assuming planarity, which of the following molecules is aromatic?</strong> A)   B)   C)   D)   E)
E) <strong>Assuming planarity, which of the following molecules is aromatic?</strong> A)   B)   C)   D)   E)
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11
Which of the following molecular orbital diagrams
best fits that of pyrrole?
pyrrole
<strong>Which of the following molecular orbital diagrams best fits that of pyrrole? pyrrole  </strong> A)   B)   C)   D)

A) <strong>Which of the following molecular orbital diagrams best fits that of pyrrole? pyrrole  </strong> A)   B)   C)   D)
B) <strong>Which of the following molecular orbital diagrams best fits that of pyrrole? pyrrole  </strong> A)   B)   C)   D)
C) <strong>Which of the following molecular orbital diagrams best fits that of pyrrole? pyrrole  </strong> A)   B)   C)   D)
D) <strong>Which of the following molecular orbital diagrams best fits that of pyrrole? pyrrole  </strong> A)   B)   C)   D)
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