Deck 8: Delocalized Electrons: Their Effect on Stability, pka, and the Products of a Reaction - Aromaticity and Electronic Effects: an Introduction to the Reactions of Benzene
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Deck 8: Delocalized Electrons: Their Effect on Stability, pka, and the Products of a Reaction - Aromaticity and Electronic Effects: an Introduction to the Reactions of Benzene
1
Due to electron delocalization,one would predict that the carbon-oxygen bond in acetamide,CH3CONH2
A)is nonpolar.
B)has more double bond character than the carbon-oxygen bond of acetone,(CH3)2CO.
C)is longer than the carbon-oxygen bond of dimethyl ether,(CH3)2O.
D)is longer than the carbon-oxygen bond of acetone,(CH3)2CO.
E)is formed by overlapping sp3 orbitals.
A)is nonpolar.
B)has more double bond character than the carbon-oxygen bond of acetone,(CH3)2CO.
C)is longer than the carbon-oxygen bond of dimethyl ether,(CH3)2O.
D)is longer than the carbon-oxygen bond of acetone,(CH3)2CO.
E)is formed by overlapping sp3 orbitals.
is longer than the carbon-oxygen bond of acetone,(CH3)2CO.
2
Mark the most electron-rich carbon atom in the compound below with an asterisk.

3
Which of the following pairs are resonance structures? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
III
4
Does the following structures represent different compounds or resonance contributors? 

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5
Which of the following statements about benzene is correct?
A)All of the carbon atoms are sp3 hybridized.
B)It has no delocalized electrons.
C)The carbon-carbon bond length is longer than that of ethane.
D)It is a planar molecule.
E)The carbon-hydrogen bonds are not the same length.
A)All of the carbon atoms are sp3 hybridized.
B)It has no delocalized electrons.
C)The carbon-carbon bond length is longer than that of ethane.
D)It is a planar molecule.
E)The carbon-hydrogen bonds are not the same length.
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6
Draw the important resonance contributing forms for the structure shown below. 

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7
In which of the following does resonance delocalization of electron density not play a role?
A)allyl cation
B)benzyl anion
C)CO32-
D)O3
E)cyclohexyl radical
A)allyl cation
B)benzyl anion
C)CO32-
D)O3
E)cyclohexyl radical
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8
Draw the important resonance structure of 

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9
Identify the resonance hybrid.
A)
B)
C)
D)
E)A,B,and C.
A)

B)

C)

D)

E)A,B,and C.
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10
Draw the important resonance contributing forms for the structure shown below. 

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11
Give the hybridization,shape,and bond angle of a carbon in benzene.
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12
Draw two other resonance contributors for the following compound. 

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13
Which of the following statements is incorrect about benzene?
A)All of the carbon atoms are sp hybridized.
B)It has delocalized electrons.
C)The carbon-carbon bond lengths are all the same.
D)The carbon-hydrogen bond lengths are all the same.
E)All twelve atoms lie in the same plane.
A)All of the carbon atoms are sp hybridized.
B)It has delocalized electrons.
C)The carbon-carbon bond lengths are all the same.
D)The carbon-hydrogen bond lengths are all the same.
E)All twelve atoms lie in the same plane.
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14
Which of the following is not a resonance structure of the species shown? 
A)I
B)II
C)III
D)IV

A)I
B)II
C)III
D)IV
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15
Which of the following pairs are resonance structures? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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16
The delocalized π system in benzene is formed by a cyclic overlap of 6 ________ orbitals.
A)s
B)p
C)sp
D)sp2
E)sp3
A)s
B)p
C)sp
D)sp2
E)sp3
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17
Draw the important resonance structures of 

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18
Draw the arrows to go from one resonance structure to another. 

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19
Draw the important resonance structures of 

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20
Draw the important resonance contributing forms for the structure shown below. 

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21
Which of the following is the strongest acid? 

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22
Identify the most stable structure(s).
A)CH2
CH-OCH3
B)CH2-CH
OCH3
C)
D)
E)
A)CH2

B)CH2-CH

C)

D)

E)

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23
Which of the following is the most stable resonance contributor to acetic acid? 
A)
B)
C)
D)
E)

A)

B)

C)

D)

E)

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24
Which of the following statements concerning resonance contributors and resonance hybrids is not correct?
A)The fewer nearly equivalent resonance contributors are in the structure,the greater the resonance energy.
B)A resonance hybrid is more stable than the predicted stability of any of its resonance contributors.
C)The greater the number of relatively stable resonance contributors,the greater the resonance energy.
D)The greater the predicted stability of a resonance contributor,the more it contributes to the resonance hybrid.
E)none of the above
A)The fewer nearly equivalent resonance contributors are in the structure,the greater the resonance energy.
B)A resonance hybrid is more stable than the predicted stability of any of its resonance contributors.
C)The greater the number of relatively stable resonance contributors,the greater the resonance energy.
D)The greater the predicted stability of a resonance contributor,the more it contributes to the resonance hybrid.
E)none of the above
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25
Draw all major resonance contributors of the species below. 

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26
What is suggested by the fact that benzene's molar heat of hydrogenation is 36 kcal less than three times the molar heat of hydrogenation of cyclohexene?
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27
Provide the major organic product of the following reaction. 

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28
Identify the correctly drawn arrows.
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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29
Aromatic molecules contain ________ π electrons.
A)no
B)4n + 2 (with n an integer)
C)4n + 2 (where n = 0.5)
D)4n (with n an integer)
E)unpaired
A)no
B)4n + 2 (with n an integer)
C)4n + 2 (where n = 0.5)
D)4n (with n an integer)
E)unpaired
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30
In the acetate ion (CH3CO2-),which of the oxygen atoms bears a greater negative charge? Explain your answer.
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31
Draw all major resonance contributors of the species below. 

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32
Draw the arrows to go from one resonance structure to another. 

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33
Stabilization of a charged species usually happens when this species can be more accurately depicted as a hybrid of several resonance contributing forms.Why is this the case?
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34
Provide the major organic product of the following reaction. 

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35
Rate the following molecules in decreasing order of stability. 

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36
The following molecule is not aromatic.Why? 

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37
Draw all major resonance contributors of the species below. 

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38
Is the following molecule aromatic? Explain. 

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39
Draw four resonance contributors for the following structure and indicate which is the most important contributor.Explain. 

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40
Draw all major resonance contributors of the species below. 

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41
Classify the compound below as aromatic,antiaromatic,or nonaromatic.Assume planarity of the π network. 

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42
Classify cyclopheptatrienyl cation as aromatic,antiaromatic,or nonaromatic.Assume planarity of the π network.
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43
Classify the compound below as aromatic,antiaromatic,or nonaromatic.Assume planarity of the π network. 

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44
Which of the following compounds is aromatic? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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45
Which of the following is aromatic? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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46
Provide the structure of the biologically significant heterocycle pyrimidine.
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47
Is cyclooctatetraene a planar molecule? Explain.
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48
Which of the following is an aromatic hydrocarbon? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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49
Classify cyclopentadienyl cation as aromatic,antiaromatic,or nonaromatic.Assume planarity of the π network.
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50
Provide the structure of indole.
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51
Which of the following is aromatic? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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52
When cycloheptatriene is deprotonated,an anion with seven resonance forms of equal energy can be drawn.Given this fact,explain why cycloheptatriene is only slightly more acidic than propene.
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53
Which of the structures below would be aromatic? 
A)I and IV
B)I,III,and IV
C)III and IV
D)II

A)I and IV
B)I,III,and IV
C)III and IV
D)II
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54
Provide the structure of the biologically significant heterocycle purine.
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55
Is the following molecule aromatic? Explain. 

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56
Cyclic hydrocarbons which can be represented as structures containing alternating single and double bonds are called ________.
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57
Which of the following is aromatic? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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58
One of the following compounds is aromatic and the other is antiaromatic.Which is which? 

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59
Which of the following is aromatic?
A)cyclopentadienyl cation
B)1,3-cyclohexadiene
C)cyclobutenyl anion
D)1,3,5-hexatriene
E)cycloheptatrienyl cation
A)cyclopentadienyl cation
B)1,3-cyclohexadiene
C)cyclobutenyl anion
D)1,3,5-hexatriene
E)cycloheptatrienyl cation
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60
Which of the following is antiaromatic? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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61
What descriptive term is applied to the type of diene represented by 2,4-hexadiene?
A)conjugated diene
B)cumulated diene
C)isolated diene
D)alkynyl diene
E)none of the above
A)conjugated diene
B)cumulated diene
C)isolated diene
D)alkynyl diene
E)none of the above
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62
Which of the following compounds contains the longest carbon-carbon single bond?
A)allene
B)1,3-butadiyne
C)1,3-butadiene
D)propyne
E)ethane
A)allene
B)1,3-butadiyne
C)1,3-butadiene
D)propyne
E)ethane
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63
Which of the following is a benzylic cation? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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64
Among a series of isomeric trienes,the more negative the ΔH° of the hydrogenation reaction of a given triene,the ________ stable it is relative to the others in the isomeric series.
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65
Which of the following is an allylic cation? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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66
Draw the distribution of π electrons in the molecular orbitals of cyclobutadiene. 

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67
Which of the following is the most stable cation? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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68
What is the hybridization of the central carbon of allene (1,2-propadiene)?
A)sp
B)sp2
C)sp3
D)p
E)none of the above
A)sp
B)sp2
C)sp3
D)p
E)none of the above
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69
Rank the following dienes in order of increasing stability: trans-1,3-pentadiene,cis-1,3-pentadiene,1,4-pentadiene,and 1,2-pentadiene.
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70
Which of the following numbered hydrogens is most easily abstracted by heterolytic cleavage? Explain. 

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71
Indicate whether the following molecule is aromatic,antiaromatic,or nonaromatic. 

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72
Which of the following compounds is more stable? Explain. 

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73
Which of the following is the most stable diene? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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74
Which of the following is a cumulated diene? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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75
How many allylic hydrogen atoms are present in the following molecule? 
A)2
B)3
C)4
D)5
E)zero

A)2
B)3
C)4
D)5
E)zero
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76
Which species is represented by the following distribution of p electrons in the molecular energy diagram? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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77
Which of the following is a conjugated diene? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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78
Which of the following statements about the π molecular orbital description of cyclobutadiene is not correct?
A)Cyclobutadiene has two degenerate nonbonding π molecular orbitals.
B)Cyclobutadiene has a single bonding π molecular orbital.
C)Cyclobutadiene has two electrons in nonbonding π molecular orbitals.
D)Cyclobutadiene has one electron in an antibonding π molecular orbital which makes it antiaromatic.
E)none of the above
A)Cyclobutadiene has two degenerate nonbonding π molecular orbitals.
B)Cyclobutadiene has a single bonding π molecular orbital.
C)Cyclobutadiene has two electrons in nonbonding π molecular orbitals.
D)Cyclobutadiene has one electron in an antibonding π molecular orbital which makes it antiaromatic.
E)none of the above
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79
What descriptive term is applied to the type of diene represented by 1,5-octadiene?
A)conjugated diene
B)cumulated diene
C)isolated diene
D)alkynyl diene
E)none of the above
A)conjugated diene
B)cumulated diene
C)isolated diene
D)alkynyl diene
E)none of the above
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80
How many benzylic hydrogens are present in the following molecule? 
A)2
B)3
C)4
D)5
E)zero

A)2
B)3
C)4
D)5
E)zero
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