Deck 17: Conjugated Pi Systems and Pericyclic Reactions

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Question
Which one of the following dienes is least stable?

A)CH3CH=CHCH=CHCH3
B)CH3CH=CHCH2CH=CH2
C)CH2=CHCH2CH2CH=CH2
D)CH2=CHCH(CH3)CH=CH2
E)CH3CH=C=CHCH2CH3
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Question
How many electrons does the HOMO of 2,4-hexadiene have in its ground state?

A)1
B)2
C)3
D)4
E)0
Question
How many electrons does the LUMO of 2,4-hexadiene have in its ground state?

A)1
B)2
C)3
D)4
E)0
Question
Predict the product for the following reaction. Predict the product for the following reaction.  <div style=padding-top: 35px>
Question
Rank the following dienes in order of decreasing heat of hydrogenation (most to least). Rank the following dienes in order of decreasing heat of hydrogenation (most to least).  <div style=padding-top: 35px>
Question
Which one of the following dienes is most stable?

A)CH3CH=CHCH=CHCH3
B)CH3CH=CHCH2CH=CH2
C)CH2=CHCH2CH2CH=CH2
D)CH2=CHCH(CH3)CH=CH2
E)CH3CH=C=CHCH2CH3
Question
Rank the following dienes in increasing order of stability (least to most). <strong>Rank the following dienes in increasing order of stability (least to most).  </strong> A)I<IV<III<II B)III<II<I<IV C)IV<II<III<I D)II<IV<III<I E)I<III<II<IV <div style=padding-top: 35px>

A)IB)IIIC)IVD)IIE)I
Question
How many π\pi -bonding molecular orbitals does 1,3-pentadiene have?

A)1
B)2
C)3
D)4
E)none
Question
Rank the following dienes in order of decreasing heat of hydrogenation (most to least). Rank the following dienes in order of decreasing heat of hydrogenation (most to least).  <div style=padding-top: 35px>
Question
Which major product(s)are formed for the following reaction? <strong>Which major product(s)are formed for the following reaction?    </strong> A)I B)II C)III D)IV E)V <div style=padding-top: 35px> <strong>Which major product(s)are formed for the following reaction?    </strong> A)I B)II C)III D)IV E)V <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
E)V
Question
Which one of the following represents the LUMO of 1,3,5-hexatriene? <strong>Which one of the following represents the LUMO of 1,3,5-hexatriene?  </strong> A)I B)II C)III D)IV E)V <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
E)V
Question
Which one of the following represents the lowest energy π\pi -bonding molecular orbital of 1,3-butadiene?  <strong>Which one of the following represents the lowest energy   \pi -bonding molecular orbital of 1,3-butadiene?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Predict the product for the following reaction. Predict the product for the following reaction.  <div style=padding-top: 35px>
Question
Which one of the following dienes is most stable? <strong>Which one of the following dienes is most stable?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Which one of the following dienes will have the highest heat of hydrogenation? <strong>Which one of the following dienes will have the highest heat of hydrogenation?  </strong> A)I B)II C)III D)IV E)V <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
E)V
Question
Which one of the following dienes is least stable? <strong>Which one of the following dienes is least stable?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
How many electrons does the HOMO of 1,3-pentadiene have in its excited state?

A)1
B)2
C)3
D)4
E)none
Question
Which one of the following represents the highest energy π\pi -antibonding molecular orbital of 1,3-butadiene?  <strong>Which one of the following represents the highest energy   \pi -antibonding molecular orbital of 1,3-butadiene?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Which one of the following represents the HOMO of 1,3,5-hexatriene? <strong>Which one of the following represents the HOMO of 1,3,5-hexatriene?  </strong> A)I B)II C)III D)IV E)V <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
E)V
Question
Which one of the following dienes will have the least heat of hydrogenation? <strong>Which one of the following dienes will have the least heat of hydrogenation?  </strong> A)I B)II C)III D)IV E)V <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
E)V
Question
The Diels Alder reaction is a concerted reaction,which means

A)The product contains a cyclic ring
B)The diene must be in the s-cis conformation to react.
C)All changes in bonding (bond making and bond breaking)occur simultaneously.
D)It is an endothermic reaction
E)Both exo and endo products are formed
Question
Provide the structure of the 1,2 addition product for the following reaction. Provide the structure of the 1,2 addition product for the following reaction.  <div style=padding-top: 35px>
Question
What is the correct classification of the following pericyclic reaction? <strong>What is the correct classification of the following pericyclic reaction?  </strong> A)electrophilic addition B)sigmatropic rearrangement C)cycloaddition D)electrocyclic reaction E)C & D <div style=padding-top: 35px>

A)electrophilic addition
B)sigmatropic rearrangement
C)cycloaddition
D)electrocyclic reaction
E)C & D
Question
Predict the major product for the following reaction and explain why it is major product. Predict the major product for the following reaction and explain why it is major product.  <div style=padding-top: 35px>
Question
What is the correct classification of the following pericyclic reaction? <strong>What is the correct classification of the following pericyclic reaction?  </strong> A)electrophilic addition B)sigmatropic rearrangement C)cycloaddition D)electrocyclic reaction E)C & D <div style=padding-top: 35px>

A)electrophilic addition
B)sigmatropic rearrangement
C)cycloaddition
D)electrocyclic reaction
E)C & D
Question
Predict the possible products for the following reaction and provide a curved arrow mechanism for the formation of these products. Predict the possible products for the following reaction and provide a curved arrow mechanism for the formation of these products.  <div style=padding-top: 35px>
Question
Predict the major product for the following reaction. Predict the major product for the following reaction.  <div style=padding-top: 35px>
Question
Which one of the following dienophiles is least reactive in the Diels-Alder reaction? <strong>Which one of the following dienophiles is least reactive in the Diels-Alder reaction?  </strong> A)I B)II C)III D)IV E)V <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
E)V
Question
Predict the possible major products for the following reaction. Predict the possible major products for the following reaction.  <div style=padding-top: 35px>
Question
Predict the product(s)for the following reaction. Predict the product(s)for the following reaction.  <div style=padding-top: 35px>
Question
Provide the structure for 1,2 addition product for the following reaction and explain why it is a major product rather than 1,4 addition product. Provide the structure for 1,2 addition product for the following reaction and explain why it is a major product rather than 1,4 addition product.  <div style=padding-top: 35px>
Question
A reaction under kinetic control will yield :

A)the most stable product.
B)the product that can be formed in the fewest steps.
C)the product whose formation requires the smallest free energy of activation.
D)the product with the greatest potential energy.
E)None of these
Question
Provide the structure of the 1,4 addition product for the reaction of 1,3-hexadiene with Br2/CCl4?
Question
A thermodynamically-controlled reaction will yield :

A)the most stable product.
B)the product whose formation requires the smallest free energy of activation.
C)the product that can be formed in the fewest steps.
D)the product that is formed at the fastest rate.
E)None of these.
Question
Which statement is NOT true about the Diels-Alder reaction?

A)It is a [4+2] cycloaddition reaction.
B)The diene must be in the s-cis conformation to react.
C)Most Diels-Alder reactions are reversible.
D)It is a sigmatropic rearrangement.
E)Electron donating groups on the diene and electron withdrawing groups on the dieneophile favor product formation.
Question
Which one of the following compounds is not a product of reaction between 1,3-butadiene and HBr?

A)(S)-3-bromo-1-butene
B)(R)-3-bromo-1-butene
C)(E)-1-bromo-2-butene
D)(Z)-1-bromo-2-butene
E)(Z)-2-bromo-2-butene
Question
Predict the major product for the following reaction. Predict the major product for the following reaction.  <div style=padding-top: 35px>
Question
What is the correct classification of the following pericyclic reaction? <strong>What is the correct classification of the following pericyclic reaction?  </strong> A)electrophilic addition B)sigmatropic rearrangement C)cycloaddition D)electrocyclic reaction E)C & D <div style=padding-top: 35px>

A)electrophilic addition
B)sigmatropic rearrangement
C)cycloaddition
D)electrocyclic reaction
E)C & D
Question
Which of the following diene(s)can not undergo the Diels-Alder reaction? <strong>Which of the following diene(s)can not undergo the Diels-Alder reaction?  </strong> A)I B)II C)III D)IV E)I & IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
E)I & IV
Question
Predict the major product for the following reaction. Predict the major product for the following reaction.  <div style=padding-top: 35px>
Question
Which is the most energetically favorable UV transition for 1,3-butadiene?.

A)n \rightarrow σ\sigma *
B)n \rightarrow π\pi *
C). π\pi 2 \rightarrowπ\pi 3*
D). σ\sigma \rightarrow σ\sigma *
E). π\pi 1 \rightarrowπ\pi 4*
Question
Which of the following compound(s)have the longest λ\lambda max?  <strong>Which of the following compound(s)have the longest  \lambda <sub>max</sub>?  </strong> A)I B)II C)III D)IV E)V <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
E)V
Question
Which of the following compound(s)have the longest λ\lambda max?  <strong>Which of the following compound(s)have the longest  \lambda <sub>max</sub>?  </strong> A)I B)II C)III D)IV E)V <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
E)V
Question
Absorption of UV-visible radiation by a molecule results in___________ transitions.

A)electronic
B)nuclear
C)rotational
D)vibrational
E)None of these
Question
Which of the following compound(s)have the longest λ\lambda max?

A)(E)2-pentene
B)(Z)2-pentene
C).1-pentene
D).1,3-hexadiene
E).1,3,5-hexatriene
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Deck 17: Conjugated Pi Systems and Pericyclic Reactions
1
Which one of the following dienes is least stable?

A)CH3CH=CHCH=CHCH3
B)CH3CH=CHCH2CH=CH2
C)CH2=CHCH2CH2CH=CH2
D)CH2=CHCH(CH3)CH=CH2
E)CH3CH=C=CHCH2CH3
CH3CH=C=CHCH2CH3
2
How many electrons does the HOMO of 2,4-hexadiene have in its ground state?

A)1
B)2
C)3
D)4
E)0
2
3
How many electrons does the LUMO of 2,4-hexadiene have in its ground state?

A)1
B)2
C)3
D)4
E)0
0
4
Predict the product for the following reaction. Predict the product for the following reaction.
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5
Rank the following dienes in order of decreasing heat of hydrogenation (most to least). Rank the following dienes in order of decreasing heat of hydrogenation (most to least).
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6
Which one of the following dienes is most stable?

A)CH3CH=CHCH=CHCH3
B)CH3CH=CHCH2CH=CH2
C)CH2=CHCH2CH2CH=CH2
D)CH2=CHCH(CH3)CH=CH2
E)CH3CH=C=CHCH2CH3
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7
Rank the following dienes in increasing order of stability (least to most). <strong>Rank the following dienes in increasing order of stability (least to most).  </strong> A)I<IV<III<II B)III<II<I<IV C)IV<II<III<I D)II<IV<III<I E)I<III<II<IV

A)IB)IIIC)IVD)IIE)I
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8
How many π\pi -bonding molecular orbitals does 1,3-pentadiene have?

A)1
B)2
C)3
D)4
E)none
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9
Rank the following dienes in order of decreasing heat of hydrogenation (most to least). Rank the following dienes in order of decreasing heat of hydrogenation (most to least).
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10
Which major product(s)are formed for the following reaction? <strong>Which major product(s)are formed for the following reaction?    </strong> A)I B)II C)III D)IV E)V <strong>Which major product(s)are formed for the following reaction?    </strong> A)I B)II C)III D)IV E)V

A)I
B)II
C)III
D)IV
E)V
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11
Which one of the following represents the LUMO of 1,3,5-hexatriene? <strong>Which one of the following represents the LUMO of 1,3,5-hexatriene?  </strong> A)I B)II C)III D)IV E)V

A)I
B)II
C)III
D)IV
E)V
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12
Which one of the following represents the lowest energy π\pi -bonding molecular orbital of 1,3-butadiene?  <strong>Which one of the following represents the lowest energy   \pi -bonding molecular orbital of 1,3-butadiene?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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13
Predict the product for the following reaction. Predict the product for the following reaction.
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14
Which one of the following dienes is most stable? <strong>Which one of the following dienes is most stable?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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15
Which one of the following dienes will have the highest heat of hydrogenation? <strong>Which one of the following dienes will have the highest heat of hydrogenation?  </strong> 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
Which one of the following dienes is least stable? <strong>Which one of the following dienes is least stable?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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17
How many electrons does the HOMO of 1,3-pentadiene have in its excited state?

A)1
B)2
C)3
D)4
E)none
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18
Which one of the following represents the highest energy π\pi -antibonding molecular orbital of 1,3-butadiene?  <strong>Which one of the following represents the highest energy   \pi -antibonding molecular orbital of 1,3-butadiene?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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19
Which one of the following represents the HOMO of 1,3,5-hexatriene? <strong>Which one of the following represents the HOMO of 1,3,5-hexatriene?  </strong> A)I B)II C)III D)IV E)V

A)I
B)II
C)III
D)IV
E)V
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20
Which one of the following dienes will have the least heat of hydrogenation? <strong>Which one of the following dienes will have the least heat of hydrogenation?  </strong> A)I B)II C)III D)IV E)V

A)I
B)II
C)III
D)IV
E)V
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21
The Diels Alder reaction is a concerted reaction,which means

A)The product contains a cyclic ring
B)The diene must be in the s-cis conformation to react.
C)All changes in bonding (bond making and bond breaking)occur simultaneously.
D)It is an endothermic reaction
E)Both exo and endo products are formed
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22
Provide the structure of the 1,2 addition product for the following reaction. Provide the structure of the 1,2 addition product for the following reaction.
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23
What is the correct classification of the following pericyclic reaction? <strong>What is the correct classification of the following pericyclic reaction?  </strong> A)electrophilic addition B)sigmatropic rearrangement C)cycloaddition D)electrocyclic reaction E)C & D

A)electrophilic addition
B)sigmatropic rearrangement
C)cycloaddition
D)electrocyclic reaction
E)C & D
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24
Predict the major product for the following reaction and explain why it is major product. Predict the major product for the following reaction and explain why it is major product.
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25
What is the correct classification of the following pericyclic reaction? <strong>What is the correct classification of the following pericyclic reaction?  </strong> A)electrophilic addition B)sigmatropic rearrangement C)cycloaddition D)electrocyclic reaction E)C & D

A)electrophilic addition
B)sigmatropic rearrangement
C)cycloaddition
D)electrocyclic reaction
E)C & D
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26
Predict the possible products for the following reaction and provide a curved arrow mechanism for the formation of these products. Predict the possible products for the following reaction and provide a curved arrow mechanism for the formation of these products.
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27
Predict the major product for the following reaction. Predict the major product for the following reaction.
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28
Which one of the following dienophiles is least reactive in the Diels-Alder reaction? <strong>Which one of the following dienophiles is least reactive in the Diels-Alder reaction?  </strong> A)I B)II C)III D)IV E)V

A)I
B)II
C)III
D)IV
E)V
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29
Predict the possible major products for the following reaction. Predict the possible major products for the following reaction.
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30
Predict the product(s)for the following reaction. Predict the product(s)for the following reaction.
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31
Provide the structure for 1,2 addition product for the following reaction and explain why it is a major product rather than 1,4 addition product. Provide the structure for 1,2 addition product for the following reaction and explain why it is a major product rather than 1,4 addition product.
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32
A reaction under kinetic control will yield :

A)the most stable product.
B)the product that can be formed in the fewest steps.
C)the product whose formation requires the smallest free energy of activation.
D)the product with the greatest potential energy.
E)None of these
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33
Provide the structure of the 1,4 addition product for the reaction of 1,3-hexadiene with Br2/CCl4?
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34
A thermodynamically-controlled reaction will yield :

A)the most stable product.
B)the product whose formation requires the smallest free energy of activation.
C)the product that can be formed in the fewest steps.
D)the product that is formed at the fastest rate.
E)None of these.
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35
Which statement is NOT true about the Diels-Alder reaction?

A)It is a [4+2] cycloaddition reaction.
B)The diene must be in the s-cis conformation to react.
C)Most Diels-Alder reactions are reversible.
D)It is a sigmatropic rearrangement.
E)Electron donating groups on the diene and electron withdrawing groups on the dieneophile favor product formation.
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36
Which one of the following compounds is not a product of reaction between 1,3-butadiene and HBr?

A)(S)-3-bromo-1-butene
B)(R)-3-bromo-1-butene
C)(E)-1-bromo-2-butene
D)(Z)-1-bromo-2-butene
E)(Z)-2-bromo-2-butene
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37
Predict the major product for the following reaction. Predict the major product for the following reaction.
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38
What is the correct classification of the following pericyclic reaction? <strong>What is the correct classification of the following pericyclic reaction?  </strong> A)electrophilic addition B)sigmatropic rearrangement C)cycloaddition D)electrocyclic reaction E)C & D

A)electrophilic addition
B)sigmatropic rearrangement
C)cycloaddition
D)electrocyclic reaction
E)C & D
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39
Which of the following diene(s)can not undergo the Diels-Alder reaction? <strong>Which of the following diene(s)can not undergo the Diels-Alder reaction?  </strong> A)I B)II C)III D)IV E)I & IV

A)I
B)II
C)III
D)IV
E)I & IV
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40
Predict the major product for the following reaction. Predict the major product for the following reaction.
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41
Which is the most energetically favorable UV transition for 1,3-butadiene?.

A)n \rightarrow σ\sigma *
B)n \rightarrow π\pi *
C). π\pi 2 \rightarrowπ\pi 3*
D). σ\sigma \rightarrow σ\sigma *
E). π\pi 1 \rightarrowπ\pi 4*
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42
Which of the following compound(s)have the longest λ\lambda max?  <strong>Which of the following compound(s)have the longest  \lambda <sub>max</sub>?  </strong> A)I B)II C)III D)IV E)V

A)I
B)II
C)III
D)IV
E)V
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43
Which of the following compound(s)have the longest λ\lambda max?  <strong>Which of the following compound(s)have the longest  \lambda <sub>max</sub>?  </strong> A)I B)II C)III D)IV E)V

A)I
B)II
C)III
D)IV
E)V
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44
Absorption of UV-visible radiation by a molecule results in___________ transitions.

A)electronic
B)nuclear
C)rotational
D)vibrational
E)None of these
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45
Which of the following compound(s)have the longest λ\lambda max?

A)(E)2-pentene
B)(Z)2-pentene
C).1-pentene
D).1,3-hexadiene
E).1,3,5-hexatriene
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