Deck 16: Conjugation, Resonance, and Dienes

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Question
Rank the following dienes in order of increasing reactivity in a Diels-Alder reaction, listing the least reactive first. <strong>Rank the following dienes in order of increasing reactivity in a Diels-Alder reaction, listing the least reactive first.  </strong> A)I< II < III B)III < I < II C)II < I < III D)I < III < II <div style=padding-top: 35px>

A)I< II < III
B)III < I < II
C)II < I < III
D)I < III < II
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Question
Which of the following statements about resonance structures is true?

A)The placement of atoms is different.
B)The placement of p bonds is different.
C)The placement of s bonds is different.
D)The placement of nonbonded electrons is the same.
Question
Rank the following compounds in order of increasing stability, putting the least stable first. <strong>Rank the following compounds in order of increasing stability, putting the least stable first.  </strong> A)I< II < III B)III < II < I C)II < I < III D)III < I < II <div style=padding-top: 35px>

A)I< II < III
B)III < II < I
C)II < I < III
D)III < I < II
Question
Which of the following statements about the Diels-Alder reaction is true?

A)The diene can react only when it adopts the s-trans conformation.
B)Electron-withdrawing substituents in the diene increase reaction rate.
C)Electron-donating substituents in the dienophile increase the reaction rate.
D)The stereochemistry of the dienophile is retained in the product.
Question
Which of the following is (are) conjugated dienes?
<strong>Which of the following is (are) conjugated dienes?  </strong> A)Only I B)Only II C)Only I and II D)I, II, and III <div style=padding-top: 35px>

A)Only I
B)Only II
C)Only I and II
D)I, II, and III
Question
Which of the following statements about the mechanism of the Diels-Alder reaction is true?

A)Three π bonds break; two σ bonds and one π bond form.
B)Three π bonds break; one σ bond and two π bonds form.
C)Two π bonds break; one σ bond and one π bond form.
D)Two π bonds break; two σ bonds and one π bond form.
Question
Which of the following is the least reactive diene in a Diels-Alder reaction?
<strong>Which of the following is the least reactive diene in a Diels-Alder reaction?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
What is the thermodynamic product obtained from the addition of 1 equivalent of HBr to 1,3-butadiene?

A)3-Bromo-1-butene
B)1-Bromo-2-butene
C)2-Bromo-2-butene
D)2-Bromo-1-butene
Question
What is (are) the major product(s) of the following reaction?
<strong>What is (are) the major product(s) of the following reaction?  </strong> A)Only I B)Only II C)Only I and II D)I, II, and III <div style=padding-top: 35px>

A)Only I
B)Only II
C)Only I and II
D)I, II, and III
Question
What is (are) the major product(s) of the following reaction?
<strong>What is (are) the major product(s) of the following reaction?  </strong> A)Only I B)Only II and IV C)Only I and III D)Only I, II, and III <div style=padding-top: 35px>

A)Only I
B)Only II and IV
C)Only I and III
D)Only I, II, and III
Question
Which of the following dienes contain conjugated double bonds?
<strong>Which of the following dienes contain conjugated double bonds?  </strong> A)Only I and II B)Only II and III C)Only I and III D)Only II and IV <div style=padding-top: 35px>

A)Only I and II
B)Only II and III
C)Only I and III
D)Only II and IV
Question
Which of the following is not a product obtained from the addition of 1 equivalent of HBr to (E)-1,3-pentadiene?

A)(E)-4-Bromo-2-pentene
B)(E)-1-Bromo-2-pentene
C)3-Bromo-1-pentene
D)(E)-3-Bromo-2-pentene
Question
What is (are) the major product(s) of the following reaction?
<strong>What is (are) the major product(s) of the following reaction?  </strong> A)Only I B)Only I and III C)Only II and IV D)Only I, II, and III <div style=padding-top: 35px>

A)Only I
B)Only I and III
C)Only II and IV
D)Only I, II, and III
Question
Which of the following is not a feature of the Diels-Alder reaction?

A)They are initiated by peroxides.
B)They form new six-membered rings.
C)Three π bonds break.
D)They are concerted.
Question
What is the kinetic product obtained from the addition of 1 equivalent of HBr to 1,3-butadiene?

A)3-Bromo-1-butene
B)1-Bromo-2-butene
C)2-Bromo-2-butene
D)2-Bromo-1-butene
Question
Which of the following is the appropriate term for the mechanism of the addition of HBr to 1,3-dienes?

A)Nucleophilic addition
B)Electrophilic addition
C)Free radical addition
D)Conjugate addition
Question
Which of the following statements about kinetic vs.thermodynamic products is true?

A)The product that is formed faster is the thermodynamic product.
B)The kinetic product predominates at low temperature.
C)The product that predominates at equilibrium is the kinetic product.
D)The thermodynamic product is less stable.
Question
What is the reactive intermediate in the reaction of 1,3-diene with HBr, resulting in 1,4-addition?

A)Allylic radical
B)Cyclic bromonium
C)Dienophile
D)Allylic carbocation
Question
What is the hybridization around the indicated carbon atom in the following anion?
<strong>What is the hybridization around the indicated carbon atom in the following anion?  </strong> A)sp<sup>3</sup> B)sp<sup>2</sup> C)sp D)p <div style=padding-top: 35px>

A)sp3
B)sp2
C)sp
D)p
Question
Which of the following conjugated dienes represent two conformations?
<strong>Which of the following conjugated dienes represent two conformations?  </strong> A)Only I and II B)Only I and III C)Only II and III D)None of the choices <div style=padding-top: 35px>

A)Only I and II
B)Only I and III
C)Only II and III
D)None of the choices
Question
Rank the following dienophile in order of increasing reactivity in a Diels-Alder reaction, listing the least reactive first. <strong><sup> </sup>Rank the following dienophile in order of increasing reactivity in a Diels-Alder reaction, listing the least reactive first.  </strong> A)I< II < III B)III < I < II C)II < I < III D)III < II < I <div style=padding-top: 35px>

A)I< II < III
B)III < I < II
C)II < I < III
D)III < II < I
Question
Which of the following compounds is the least reactive dienophile in a Diels-Alder reaction?
<strong>Which of the following compounds is the least reactive dienophile in a Diels-Alder reaction?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Which of the following is the most reactive diene in a Diels-Alder reaction?
<strong>Which of the following is the most reactive diene in a Diels-Alder reaction?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
What is the major organic product of the following reaction?
<strong>What is the major organic product of the following reaction?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Why would the compound below not react with a dienophile in a Diels-Alder reaction?
<strong>Why would the compound below not react with a dienophile in a Diels-Alder reaction?  </strong> A)The compound is not a conjugated diene. B)There are no electron withdrawing groups on the compound. C)There are no electron donating groups on the compound. D)The compound cannot adopt the s-cis conformation. <div style=padding-top: 35px>

A)The compound is not a conjugated diene.
B)There are no electron withdrawing groups on the compound.
C)There are no electron donating groups on the compound.
D)The compound cannot adopt the s-cis conformation.
Question
Which of the following electronic transitions is common in the UV spectrum of 1,3-butadiene?

A)sp
B)sp*
C)n p*
D)pp*
Question
What is the definition of a resonance structure?

A)Compounds with the same molecular formula.
B)Compounds with different carbon frameworks.
C)Structures that differ only in the placement of π and nonbonding electrons.
D)Structures that differ only in the location of bonds.
Question
Which of the following compound absorbs UV light at the longest wavelength?
<strong>Which of the following compound absorbs UV light at the longest wavelength?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Which of the following compounds is the most reactive dienophile in a Diels-Alder reaction?
<strong>Which of the following compounds is the most reactive dienophile in a Diels-Alder reaction?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Which of the following is an example of a bridged bicyclic system?
<strong>Which of the following is an example of a bridged bicyclic system?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
What is the major organic product of the following reaction?
<strong>What is the major organic product of the following reaction?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
What is the major organic product of the following reaction?
<strong>What is the major organic product of the following reaction?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Which of the following is the least reactive diene in a Diels-Alder reaction?
<strong>Which of the following is the least reactive diene in a Diels-Alder reaction?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
What is the major organic product of the following reaction?
<strong>What is the major organic product of the following reaction?  </strong> A)Only I B)Only II C)Only III D)Only I and II <div style=padding-top: 35px>

A)Only I
B)Only II
C)Only III
D)Only I and II
Question
Which of the following is not a resonance structure of acetic anhydride?
<strong>Which of the following is not a resonance structure of acetic anhydride?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Rank the following anions from most to least stable, listing the most stable first. <strong>Rank the following anions from most to least stable, listing the most stable first.  </strong> A)I> II > III B)III > II > I C)I > III > II D)III > I > II <div style=padding-top: 35px>

A)I> II > III
B)III > II > I
C)I > III > II
D)III > I > II
Question
What diene and dienophile are used in a Diels-Alder reaction to prepare the following compound?
<strong>What diene and dienophile are used in a Diels-Alder reaction to prepare the following compound?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
What is the major organic product of the following reaction?
<strong>What is the major organic product of the following reaction?  </strong> A)Only I B)Only I and II C)Only II and III D)I, II, and III <div style=padding-top: 35px>

A)Only I
B)Only I and II
C)Only II and III
D)I, II, and III
Question
What is the major organic product of the following reaction?
<strong>What is the major organic product of the following reaction?  </strong> A)Only I B)Only II C)Only III D)Only I and II <div style=padding-top: 35px>

A)Only I
B)Only II
C)Only III
D)Only I and II
Question
Which of the following compound absorbs UV light at the longest wavelength?
<strong>Which of the following compound absorbs UV light at the longest wavelength?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Which triene absorbs the longest wavelength of UV light?
<strong>Which triene absorbs the longest wavelength of UV light?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Which triene has the smallest heat of hydrogenation?
<strong>Which triene has the smallest heat of hydrogenation?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Which triene has the largest heat of hydrogenation?
<strong>Which triene has the largest heat of hydrogenation?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
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Deck 16: Conjugation, Resonance, and Dienes
1
Rank the following dienes in order of increasing reactivity in a Diels-Alder reaction, listing the least reactive first. <strong>Rank the following dienes in order of increasing reactivity in a Diels-Alder reaction, listing the least reactive first.  </strong> A)I< II < III B)III < I < II C)II < I < III D)I < III < II

A)I< II < III
B)III < I < II
C)II < I < III
D)I < III < II
III < I < II
2
Which of the following statements about resonance structures is true?

A)The placement of atoms is different.
B)The placement of p bonds is different.
C)The placement of s bonds is different.
D)The placement of nonbonded electrons is the same.
The placement of p bonds is different.
3
Rank the following compounds in order of increasing stability, putting the least stable first. <strong>Rank the following compounds in order of increasing stability, putting the least stable first.  </strong> A)I< II < III B)III < II < I C)II < I < III D)III < I < II

A)I< II < III
B)III < II < I
C)II < I < III
D)III < I < II
I< II < III
4
Which of the following statements about the Diels-Alder reaction is true?

A)The diene can react only when it adopts the s-trans conformation.
B)Electron-withdrawing substituents in the diene increase reaction rate.
C)Electron-donating substituents in the dienophile increase the reaction rate.
D)The stereochemistry of the dienophile is retained in the product.
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5
Which of the following is (are) conjugated dienes?
<strong>Which of the following is (are) conjugated dienes?  </strong> A)Only I B)Only II C)Only I and II D)I, II, and III

A)Only I
B)Only II
C)Only I and II
D)I, II, and III
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6
Which of the following statements about the mechanism of the Diels-Alder reaction is true?

A)Three π bonds break; two σ bonds and one π bond form.
B)Three π bonds break; one σ bond and two π bonds form.
C)Two π bonds break; one σ bond and one π bond form.
D)Two π bonds break; two σ bonds and one π bond form.
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7
Which of the following is the least reactive diene in a Diels-Alder reaction?
<strong>Which of the following is the least reactive diene in a Diels-Alder reaction?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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8
What is the thermodynamic product obtained from the addition of 1 equivalent of HBr to 1,3-butadiene?

A)3-Bromo-1-butene
B)1-Bromo-2-butene
C)2-Bromo-2-butene
D)2-Bromo-1-butene
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9
What is (are) the major product(s) of the following reaction?
<strong>What is (are) the major product(s) of the following reaction?  </strong> A)Only I B)Only II C)Only I and II D)I, II, and III

A)Only I
B)Only II
C)Only I and II
D)I, II, and III
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10
What is (are) the major product(s) of the following reaction?
<strong>What is (are) the major product(s) of the following reaction?  </strong> A)Only I B)Only II and IV C)Only I and III D)Only I, II, and III

A)Only I
B)Only II and IV
C)Only I and III
D)Only I, II, and III
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11
Which of the following dienes contain conjugated double bonds?
<strong>Which of the following dienes contain conjugated double bonds?  </strong> A)Only I and II B)Only II and III C)Only I and III D)Only II and IV

A)Only I and II
B)Only II and III
C)Only I and III
D)Only II and IV
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12
Which of the following is not a product obtained from the addition of 1 equivalent of HBr to (E)-1,3-pentadiene?

A)(E)-4-Bromo-2-pentene
B)(E)-1-Bromo-2-pentene
C)3-Bromo-1-pentene
D)(E)-3-Bromo-2-pentene
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13
What is (are) the major product(s) of the following reaction?
<strong>What is (are) the major product(s) of the following reaction?  </strong> A)Only I B)Only I and III C)Only II and IV D)Only I, II, and III

A)Only I
B)Only I and III
C)Only II and IV
D)Only I, II, and III
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14
Which of the following is not a feature of the Diels-Alder reaction?

A)They are initiated by peroxides.
B)They form new six-membered rings.
C)Three π bonds break.
D)They are concerted.
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15
What is the kinetic product obtained from the addition of 1 equivalent of HBr to 1,3-butadiene?

A)3-Bromo-1-butene
B)1-Bromo-2-butene
C)2-Bromo-2-butene
D)2-Bromo-1-butene
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16
Which of the following is the appropriate term for the mechanism of the addition of HBr to 1,3-dienes?

A)Nucleophilic addition
B)Electrophilic addition
C)Free radical addition
D)Conjugate addition
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17
Which of the following statements about kinetic vs.thermodynamic products is true?

A)The product that is formed faster is the thermodynamic product.
B)The kinetic product predominates at low temperature.
C)The product that predominates at equilibrium is the kinetic product.
D)The thermodynamic product is less stable.
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18
What is the reactive intermediate in the reaction of 1,3-diene with HBr, resulting in 1,4-addition?

A)Allylic radical
B)Cyclic bromonium
C)Dienophile
D)Allylic carbocation
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19
What is the hybridization around the indicated carbon atom in the following anion?
<strong>What is the hybridization around the indicated carbon atom in the following anion?  </strong> A)sp<sup>3</sup> B)sp<sup>2</sup> C)sp D)p

A)sp3
B)sp2
C)sp
D)p
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20
Which of the following conjugated dienes represent two conformations?
<strong>Which of the following conjugated dienes represent two conformations?  </strong> A)Only I and II B)Only I and III C)Only II and III D)None of the choices

A)Only I and II
B)Only I and III
C)Only II and III
D)None of the choices
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21
Rank the following dienophile in order of increasing reactivity in a Diels-Alder reaction, listing the least reactive first. <strong><sup> </sup>Rank the following dienophile in order of increasing reactivity in a Diels-Alder reaction, listing the least reactive first.  </strong> A)I< II < III B)III < I < II C)II < I < III D)III < II < I

A)I< II < III
B)III < I < II
C)II < I < III
D)III < II < I
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22
Which of the following compounds is the least reactive dienophile in a Diels-Alder reaction?
<strong>Which of the following compounds is the least reactive dienophile in a Diels-Alder reaction?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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23
Which of the following is the most reactive diene in a Diels-Alder reaction?
<strong>Which of the following is the most reactive diene in a Diels-Alder reaction?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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24
What is the major organic product of the following reaction?
<strong>What is the major organic product of the following reaction?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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25
Why would the compound below not react with a dienophile in a Diels-Alder reaction?
<strong>Why would the compound below not react with a dienophile in a Diels-Alder reaction?  </strong> A)The compound is not a conjugated diene. B)There are no electron withdrawing groups on the compound. C)There are no electron donating groups on the compound. D)The compound cannot adopt the s-cis conformation.

A)The compound is not a conjugated diene.
B)There are no electron withdrawing groups on the compound.
C)There are no electron donating groups on the compound.
D)The compound cannot adopt the s-cis conformation.
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26
Which of the following electronic transitions is common in the UV spectrum of 1,3-butadiene?

A)sp
B)sp*
C)n p*
D)pp*
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27
What is the definition of a resonance structure?

A)Compounds with the same molecular formula.
B)Compounds with different carbon frameworks.
C)Structures that differ only in the placement of π and nonbonding electrons.
D)Structures that differ only in the location of bonds.
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28
Which of the following compound absorbs UV light at the longest wavelength?
<strong>Which of the following compound absorbs UV light at the longest wavelength?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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29
Which of the following compounds is the most reactive dienophile in a Diels-Alder reaction?
<strong>Which of the following compounds is the most reactive dienophile in a Diels-Alder reaction?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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30
Which of the following is an example of a bridged bicyclic system?
<strong>Which of the following is an example of a bridged bicyclic system?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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31
What is the major organic product of the following reaction?
<strong>What is the major organic product of the following reaction?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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32
What is the major organic product of the following reaction?
<strong>What is the major organic product of the following reaction?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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33
Which of the following is the least reactive diene in a Diels-Alder reaction?
<strong>Which of the following is the least reactive diene in a Diels-Alder reaction?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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34
What is the major organic product of the following reaction?
<strong>What is the major organic product of the following reaction?  </strong> A)Only I B)Only II C)Only III D)Only I and II

A)Only I
B)Only II
C)Only III
D)Only I and II
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35
Which of the following is not a resonance structure of acetic anhydride?
<strong>Which of the following is not a resonance structure of acetic anhydride?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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36
Rank the following anions from most to least stable, listing the most stable first. <strong>Rank the following anions from most to least stable, listing the most stable first.  </strong> A)I> II > III B)III > II > I C)I > III > II D)III > I > II

A)I> II > III
B)III > II > I
C)I > III > II
D)III > I > II
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37
What diene and dienophile are used in a Diels-Alder reaction to prepare the following compound?
<strong>What diene and dienophile are used in a Diels-Alder reaction to prepare the following compound?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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38
What is the major organic product of the following reaction?
<strong>What is the major organic product of the following reaction?  </strong> A)Only I B)Only I and II C)Only II and III D)I, II, and III

A)Only I
B)Only I and II
C)Only II and III
D)I, II, and III
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39
What is the major organic product of the following reaction?
<strong>What is the major organic product of the following reaction?  </strong> A)Only I B)Only II C)Only III D)Only I and II

A)Only I
B)Only II
C)Only III
D)Only I and II
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40
Which of the following compound absorbs UV light at the longest wavelength?
<strong>Which of the following compound absorbs UV light at the longest wavelength?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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41
Which triene absorbs the longest wavelength of UV light?
<strong>Which triene absorbs the longest wavelength of UV light?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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42
Which triene has the smallest heat of hydrogenation?
<strong>Which triene has the smallest heat of hydrogenation?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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43
Which triene has the largest heat of hydrogenation?
<strong>Which triene has the largest heat of hydrogenation?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
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Unlock Deck
Unlock for access to all 43 flashcards in this deck.