Deck 8: Delocalized Electrons Their Eff
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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.
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?

A)
B)
C)
D)
E)

A)

B)

C)

D)

E)


3
Which structure makes the largest contribution to the resonance hybrid?
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)


4
Which of the following is the strongest acid?
A)
B)
C)
D)
E)
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? 
A)
B)
C)
D)
E)

A)

B)

C)

D)

E)

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6
Which diene will react most readily with a dienophile?
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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7
Which compound is the expected product of this reaction? 
A)
B)
C)
D)
E)

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.
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? 
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)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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11
Which of the following molecular orbital diagrams
best fits that of pyrrole?
pyrrole

A)
B)
C)
D)
best fits that of pyrrole?
pyrrole

A)

B)

C)

D)

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