Deck 20: Dienes, Conjugated Systems, and Pericyclic Reactions

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Question
What is the correct order of exothermicity for hydrogenation of the following hexadienes upon treatment with H2/Pd (more exothermic > less exothermic)? <strong>What is the correct order of exothermicity for hydrogenation of the following hexadienes upon treatment with H<sub>2</sub>/Pd (more exothermic > less exothermic)?  </strong> A) 1 > 2 > 3 B) 3 > 1 > 2 C) 2 > 1 > 3 D) 3 > 2 > 1 <div style=padding-top: 35px>

A) 1 > 2 > 3
B) 3 > 1 > 2
C) 2 > 1 > 3
D) 3 > 2 > 1
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Question
Which of the following alkenes undergoes the least exothermic hydrogenation upon treatment with H2/Pd <strong>Which of the following alkenes undergoes the least exothermic hydrogenation upon treatment with H<sub>2</sub>/Pd  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Which of the following is(are) formed upon addition of 1 mol of Br2 to 1,3-cyclohexane? <strong>Which of the following is(are) formed upon addition of 1 mol of Br<sub>2</sub> to 1,3-cyclohexane?  </strong> A) only 2 B) only 1 and 3 C) only 2 and 4 D) 1, 2 and 3 <div style=padding-top: 35px>

A) only 2
B) only 1 and 3
C) only 2 and 4
D) 1, 2 and 3
Question
What is (are) the major organic product(s) formed in the following reaction? <strong>What is (are) the major organic product(s) formed in the following reaction?  </strong> A) only 1 B) only 3 C) only 1 and 3 D) only 2 and 4 <div style=padding-top: 35px>

A) only 1
B) only 3
C) only 1 and 3
D) only 2 and 4
Question
What is the IUPAC name of the following compound? <strong>What is the IUPAC name of the following compound?  </strong> A) 2,3-dimethyl-2,4-pentadiene B) (Z)-2,3-dimethyl-2,4-pentadiene C) 3,4-dimethyl-1,3-pentadiene D) (Z)-3,4-dimethyl-1,3-pentadiene <div style=padding-top: 35px>

A) 2,3-dimethyl-2,4-pentadiene
B) (Z)-2,3-dimethyl-2,4-pentadiene
C) 3,4-dimethyl-1,3-pentadiene
D) (Z)-3,4-dimethyl-1,3-pentadiene
Question
Which of the following are conjugated dienes? <strong>Which of the following are conjugated dienes?  </strong> A) only 1 B) only 2 C) only 1 and 2 D) 1, 2 and 3 <div style=padding-top: 35px>

A) only 1
B) only 2
C) only 1 and 2
D) 1, 2 and 3
Question
Which of the following terms describes the mechanism for the addition of Br2 to butadiene?

A) electrophilic addition
B) nucleophilic addition
C) pericyclic addition
D) conjugate addition
Question
What is the kinetic product obtained from the addition of 1 mole of bromine to 1,3-butadiene?

A) 3,4-dibromo-1-butene
B) (E)-1,4-dibromo-2-butene
C) (Z)-1,4-dibromo-2-butene
D) (Z)-2,3-dibromo-2-butene
Question
Which of the following is not a major organic product obtained from the addition of 1 mole of bromine to (E)-1,3-pentadiene?

A) (E)-4,5-dibromo-2-pentene
B) 3,4-dibromo-1-pentene
C) (E)-1,4-dibromo-2-pentene
D) (E)-1,2-dibromo-2-pentene
Question
What is (are) the major organic product(s) formed in the following reaction? <strong>What is (are) the major organic product(s) formed in the following reaction?  </strong> A) only 1 B) only 1 and 2 C) only 1 and 3 D) only 2 and 4 <div style=padding-top: 35px>

A) only 1
B) only 1 and 2
C) only 1 and 3
D) only 2 and 4
Question
What is the reactive intermediate in the reaction of 1,3-butadiene with HBr resulting in 1,2-addition?

A) cyclic bromonium cation
B) allylic cation
C) allylic radical
D) dienophile
Question
Which of the following arrangements of p atomic orbitals gives the highest energy π-antibonding molecular orbital of 1,3-butadiene? <strong>Which of the following arrangements of p atomic orbitals gives the highest energy π-antibonding molecular orbital of 1,3-butadiene?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
What is the systematic IUPAC name of the following compound? <strong>What is the systematic IUPAC name of the following compound?  </strong> A) (3S,4E)-3-ethyl-3,4-dimethyl-1,4-hexadiene B) (3R,4E)-3-ethyl-3,4-dimethyl-1,4-hexadiene C) (3S,4Z)-3-ethyl-3,4-dimethyl-1,4-hexadiene D) (3R,4Z)-3-ethyl-3,4-dimethyl-1,4-hexadiene <div style=padding-top: 35px>

A) (3S,4E)-3-ethyl-3,4-dimethyl-1,4-hexadiene
B) (3R,4E)-3-ethyl-3,4-dimethyl-1,4-hexadiene
C) (3S,4Z)-3-ethyl-3,4-dimethyl-1,4-hexadiene
D) (3R,4Z)-3-ethyl-3,4-dimethyl-1,4-hexadiene
Question
Which of the following arrangements of p atomic orbitals gives the lowest energy π-bonding molecular orbital of 1,3-butadiene? <strong>Which of the following arrangements of p atomic orbitals gives the lowest energy π-bonding molecular orbital of 1,3-butadiene?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
What is the thermodynamic product obtained from the addition of 1 mole of bromine to 1,3-butadiene?

A) 3,4-dibromo-1-butene
B) (E)-1,4-dibromo-2-butene
C) (Z)-1,4-dibromo-2-butene
D) (Z)-2,3-dibromo-2-butene
Question
What is (are) the major organic product(s) formed in the following reaction? <strong>What is (are) the major organic product(s) formed in the following reaction?  </strong> A) only 1 B) only 2 C) only 1 and 3 D) only 2 and 4 <div style=padding-top: 35px>

A) only 1
B) only 2
C) only 1 and 3
D) only 2 and 4
Question
Which of the following are conjugated dienes? <strong>Which of the following are conjugated dienes?  </strong> A) only 1 B) only 2 C) only 1 and 2 D) 1, 2 and 3 <div style=padding-top: 35px>

A) only 1
B) only 2
C) only 1 and 2
D) 1, 2 and 3
Question
What is (are) the major organic product(s) formed in the following reaction? <strong>What is (are) the major organic product(s) formed in the following reaction?  </strong> A) only 1 B) only 1 and 3 C) only 2 and 4 D) only 1 and 4 <div style=padding-top: 35px>

A) only 1
B) only 1 and 3
C) only 2 and 4
D) only 1 and 4
Question
Which of the following arrangements of p atomic orbitals of 1,3-butadiene has the greatest number of nodes? <strong>Which of the following arrangements of p atomic orbitals of 1,3-butadiene has the greatest number of nodes?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
What is the IUPAC name of the following compound? <strong>What is the IUPAC name of the following compound?  </strong> A) (R)-3-vinyl-1-butene B) 3-methyl-1,5-pentadiene C) 3-methyl-1,4-pentadiene D) (R)-3-methyl-1,4-pentadiene <div style=padding-top: 35px>

A) (R)-3-vinyl-1-butene
B) 3-methyl-1,5-pentadiene
C) 3-methyl-1,4-pentadiene
D) (R)-3-methyl-1,4-pentadiene
Question
Which of the following has the highest value of λmax in the ultraviolet-visible spectrum? <strong>Which of the following has the highest value of λ<sub>max</sub> in the ultraviolet-visible spectrum?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
What are the units of λmax in ultraviolet-visible spectroscopy?

A) J⋅mol−1
B) M−1
C) nm
D) none, λmax is a dimensionless quantity
Question
For a diene to undergo a Diels-Alder reaction it must be able to adopt an s-trans conformation.
Question
Which of the following energy diagrams represents the electronic state of butadiene after absorption of radiation? <strong>Which of the following energy diagrams represents the electronic state of butadiene after absorption of radiation?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Which of the following relationships is not valid as applied to ultraviolet-visible spectroscopy?

A) A = log (Io/I)
B) A = εcl
C) ΔE = hν
D) A = λmaxl
Question
The conjugated portion of the following molecule is circled. The conjugated portion of the following molecule is circled.  <div style=padding-top: 35px>
Question
Electrophilic addition reaction of conjugated dienes that occur at high temperature and/or long reaction times (reversible conditions) are said to be under kinetic control.
Question
Which of the following processes takes place upon absorption of ultraviolet-visible radiation?

A) bond vibration
B) electron excitation
C) nuclear spin flip
D) electron spin flip
Question
What range of wavelengths corresponds to the ultraviolet region of the electromagnetic spectrum?

A) 200-400 nm
B) 400-700 nm
C) 2.5-25 μm
D) 2-10 mm
Question
Which of the following has the highest value of λmax in the ultraviolet-visible spectrum? <strong>Which of the following has the highest value of λ<sub>max</sub> in the ultraviolet-visible spectrum?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Which of the following reaction coordinate diagrams explains the formation of different thermodynamic (T) and kinetic products from the same reactants (R)? <strong>Which of the following reaction coordinate diagrams explains the formation of different thermodynamic (T) and kinetic products from the same reactants (R)?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Consider the following structure. Consider the following structure.   This substance could be produced by the reaction of the following diene and dienophile.  <div style=padding-top: 35px> This substance could be produced by the reaction of the following diene and dienophile. Consider the following structure.   This substance could be produced by the reaction of the following diene and dienophile.  <div style=padding-top: 35px>
Question
The conjugated portion of the following molecule is circled. The conjugated portion of the following molecule is circled.  <div style=padding-top: 35px>
Question
Which of the following energy diagrams represents the electronic state of the ground state of 1,3-butadiene? <strong>Which of the following energy diagrams represents the electronic state of the ground state of 1,3-butadiene?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
What are the units of ε in ultraviolet-visible spectroscopy?

A) M−1⋅cm−1
B) M⋅cm
C) J⋅mol−1⋅M−1
D) none, ε is a dimensionless quantity
Question
What quantity is abbreviated as ε in ultraviolet-visible spectroscopy?

A) absorbance
B) molecular absorptivity
C) intensity of transmitted light
D) wavelength of maximum absorbance
Question
Which of the following laws relates absorbance to the concentration of a sample and the pathlength in ultraviolet-visible spectroscopy?

A) Buzz-Beer law
B) Beer-Lambert law
C) Duff-Beer law
D) Christopher-Lambert law
Question
Which of the following electronic transitions is apparent in the ultraviolet-visible spectrum of 1,3-butadiene?

A) n → π*
B) π → π *
C) σ → π *
D) σ → π
Question
What is (are) the major organic product(s) formed in the following reaction? <strong>What is (are) the major organic product(s) formed in the following reaction?  </strong> A) only 1 B) only 2 C) only 3 D) 1, 2 and 3 <div style=padding-top: 35px>

A) only 1
B) only 2
C) only 3
D) 1, 2 and 3
Question
What are the units of absorbance, A, in ultraviolet-visible spectroscopy?

A) J⋅mol−1
B) nm⋅mol−1
C) J⋅mol−1⋅M−1
D) none, A is a dimensionless quantity
Question
Consider the following reaction. Consider the following reaction.   This is an example of a sigmatropic reaction with a [3,3]-shift.<div style=padding-top: 35px> This is an example of a sigmatropic reaction with a [3,3]-shift.
Question
Consider the reaction below to answer the following question(s). Consider the reaction below to answer the following question(s).   Fill in the blank in the question with the appropriate letter. The dienophile in the reaction is ____.<div style=padding-top: 35px> Fill in the blank in the question with the appropriate letter.
The dienophile in the reaction is ____.
Question
The following spectrum could arise from π to π* transitions. The following spectrum could arise from π to π* transitions.  <div style=padding-top: 35px>
Question
Consider the reaction below to answer the following question(s): Consider the reaction below to answer the following question(s):   Enter the appropriate letter in the blank for each the following statements. The product that results from following mechanistic step is _____.  <div style=padding-top: 35px> Enter the appropriate letter in the blank for each the following statements.
The product that results from following mechanistic step is _____. Consider the reaction below to answer the following question(s):   Enter the appropriate letter in the blank for each the following statements. The product that results from following mechanistic step is _____.  <div style=padding-top: 35px>
Question
Consider the reaction below to answer the following question(s). Consider the reaction below to answer the following question(s).   Fill in the blank in the question with the appropriate letter. This is an example of a(n) ____________ reaction. A. sigmatropic reaction B. electrophillic addition C. Diels-Alder reaction D. Cope rearrangement<div style=padding-top: 35px> Fill in the blank in the question with the appropriate letter.
This is an example of a(n) ____________ reaction.
A. sigmatropic reaction
B. electrophillic addition
C. Diels-Alder reaction
D. Cope rearrangement
Question
What is the IUPAC name of the following compound? What is the IUPAC name of the following compound?  <div style=padding-top: 35px>
Question
What is the IUPAC name of the following compound? What is the IUPAC name of the following compound?  <div style=padding-top: 35px>
Question
Consider the following spectrum for a conjugated diene. Consider the following spectrum for a conjugated diene.   If a similar spectrum were taken for a conjugated tetraene, the λ<sub>max</sub> would be _________than 217 nm.<div style=padding-top: 35px> If a similar spectrum were taken for a conjugated tetraene, the λmax would be _________than 217 nm.
Question
Based on the following table.
Based on the following table.   Compound ______ has the largest energy difference between the HOMO and LUMO.<div style=padding-top: 35px>
Compound ______ has the largest energy difference between the HOMO and LUMO.
Question
The following compound could act as a diene in a Diels-Alder reaction. The following compound could act as a diene in a Diels-Alder reaction.  <div style=padding-top: 35px>
Question
Sigmatropic shifts, cycloaddition reactions and anuulation reactions are all examples of pericyclic reactions.
Question
The following two compounds could be easily distinguished by NMR, IR, UV or MS spectra. The following two compounds could be easily distinguished by NMR, IR, UV or MS spectra.  <div style=padding-top: 35px>
Question
Consider the following reaction. Consider the following reaction.   This is an example of a sigmatropic reaction with a [3,3]-shift.<div style=padding-top: 35px> This is an example of a sigmatropic reaction with a [3,3]-shift.
Question
For Diels-Alder cycloaddition reactions to take place most rapidly and in highest yield a dienophile must be substituted with electron-donating groups.
Question
Consider the reaction below to answer the following question(s): Consider the reaction below to answer the following question(s):   Enter the appropriate letter in the blank for each the following statements. The electrophile in this reaction is ____.<div style=padding-top: 35px> Enter the appropriate letter in the blank for each the following statements.
The electrophile in this reaction is ____.
Question
Consider the reaction below to answer the following question(s). Consider the reaction below to answer the following question(s).   Fill in the blank in the question with the appropriate letter. The diene in the reaction is ____.<div style=padding-top: 35px> Fill in the blank in the question with the appropriate letter.
The diene in the reaction is ____.
Question
Consider the reaction below to answer the following question(s): Consider the reaction below to answer the following question(s):   Enter the appropriate letter in the blank for each the following statements. The nucleophile in this reaction is ____.<div style=padding-top: 35px> Enter the appropriate letter in the blank for each the following statements.
The nucleophile in this reaction is ____.
Question
Consider the reaction below to answer the following question(s): Consider the reaction below to answer the following question(s):   Enter the appropriate letter in the blank for each the following statements. The product that results from 1,4-addition is _____.<div style=padding-top: 35px> Enter the appropriate letter in the blank for each the following statements.
The product that results from 1,4-addition is _____.
Question
Consider the reaction below to answer the following question(s): Consider the reaction below to answer the following question(s):   Enter the appropriate letter in the blank for each the following statements. The kinetically controlled product in this reaction is _____.<div style=padding-top: 35px> Enter the appropriate letter in the blank for each the following statements.
The kinetically controlled product in this reaction is _____.
Question
When an organic molecule is irradiated with ultraviolet radiation, the energy absorbed by the molecule corresponds to the amount necessary to excite electrons from one molecular orbital to another.
Question
Provide the structures of the constitutional isomers of the two major organic products obtained from the following reaction? Provide the structures of the constitutional isomers of the two major organic products obtained from the following reaction?  <div style=padding-top: 35px>
Question
What are the two major organic products obtained from the following reaction? What are the two major organic products obtained from the following reaction?  <div style=padding-top: 35px>
Question
Why carbonyl groups of aldehydes and ketones on conjugation with carbon-carbon double bonds show strong absorption in the ultraviolet spectrum?
Question
The molar absorptivity of ethylene in hexane is 15,000 L mol−1 cm−1. What is the maximum absorbance observed at a concentration of 1.5 x 10−4 mol L−1? (Path length = 1 cm)

A) 2.25
B) 1.25
C) 3.25
D) 2.52
Question
Which of 1,3-cyclohexadiene and 1,4-cyclohexadiene has the greatest heat of hydrogenation (i.e., the most exothermic reaction with H2 in the presence of a catalyst). Provide a brief explanation for your choice ?
Question
What is the major organic product obtained from the following reaction? What is the major organic product obtained from the following reaction?  <div style=padding-top: 35px>
Question
The [2+2] cycloaddition reaction of ethylene to form cyclobutane does not occur because _____. ​ <strong>The [2+2] cycloaddition reaction of ethylene to form cyclobutane does not occur because _____. ​  </strong> A) the reaction is forbidden as determined by the frontier molecular orbital analysis B) the reaction is allowed as determined by the frontier molecular orbital analysis C) the reaction is allowed, and ethylene collides in a suprafacial manner D) the reaction is allowed, and ethylene collides in an antarafacial manner <div style=padding-top: 35px>

A) the reaction is forbidden as determined by the frontier molecular orbital analysis
B) the reaction is allowed as determined by the frontier molecular orbital analysis
C) the reaction is allowed, and ethylene collides in a suprafacial manner
D) the reaction is allowed, and ethylene collides in an antarafacial manner
Question
How would you be able to distinguish between 1,3-cyclohexadiene and 1,4-cyclohexadiene using ultraviolet spectroscopy?
Question
What are the two major organic products obtained from the following reaction? What are the two major organic products obtained from the following reaction?  <div style=padding-top: 35px>
Question
Draw two resonance structures of the reactive intermediate that accounts for the formation of 1,2- and 1,4-addition products upon reaction of 1,3-butadiene with one equivalent of HBr.
Question
Pericyclic reactions occur in a single step with the _____.

A) formation of a radical
B) formation of an ionic intermediate
C) formation of a molecular ion
D) formation of a transition state
Question
Identify the product of the given reaction. ​ <strong>Identify the product of the given reaction. ​  </strong> A) I B) II C) IV D) III <div style=padding-top: 35px>

A) I
B) II
C) IV
D) III
Question
Identify the product of the given reaction. ​ <strong>Identify the product of the given reaction. ​  </strong> A) I B) II C) IV D) III <div style=padding-top: 35px>

A) I
B) II
C) IV
D) III
Question
Draw two resonance structures of the reactive intermediate that accounts for the formation of 1,2- and 1,4-addition products upon reaction of 1,3-butadiene with one equivalent of bromine.
Question
A reaction in which two reactants add together in a single step to form a cyclic product is known as a _____.

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Deck 20: Dienes, Conjugated Systems, and Pericyclic Reactions
1
What is the correct order of exothermicity for hydrogenation of the following hexadienes upon treatment with H2/Pd (more exothermic > less exothermic)? <strong>What is the correct order of exothermicity for hydrogenation of the following hexadienes upon treatment with H<sub>2</sub>/Pd (more exothermic > less exothermic)?  </strong> A) 1 > 2 > 3 B) 3 > 1 > 2 C) 2 > 1 > 3 D) 3 > 2 > 1

A) 1 > 2 > 3
B) 3 > 1 > 2
C) 2 > 1 > 3
D) 3 > 2 > 1
3 > 1 > 2
2
Which of the following alkenes undergoes the least exothermic hydrogenation upon treatment with H2/Pd <strong>Which of the following alkenes undergoes the least exothermic hydrogenation upon treatment with H<sub>2</sub>/Pd  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
3
3
Which of the following is(are) formed upon addition of 1 mol of Br2 to 1,3-cyclohexane? <strong>Which of the following is(are) formed upon addition of 1 mol of Br<sub>2</sub> to 1,3-cyclohexane?  </strong> A) only 2 B) only 1 and 3 C) only 2 and 4 D) 1, 2 and 3

A) only 2
B) only 1 and 3
C) only 2 and 4
D) 1, 2 and 3
only 2 and 4
4
What is (are) the major organic product(s) formed in the following reaction? <strong>What is (are) the major organic product(s) formed in the following reaction?  </strong> A) only 1 B) only 3 C) only 1 and 3 D) only 2 and 4

A) only 1
B) only 3
C) only 1 and 3
D) only 2 and 4
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5
What is the IUPAC name of the following compound? <strong>What is the IUPAC name of the following compound?  </strong> A) 2,3-dimethyl-2,4-pentadiene B) (Z)-2,3-dimethyl-2,4-pentadiene C) 3,4-dimethyl-1,3-pentadiene D) (Z)-3,4-dimethyl-1,3-pentadiene

A) 2,3-dimethyl-2,4-pentadiene
B) (Z)-2,3-dimethyl-2,4-pentadiene
C) 3,4-dimethyl-1,3-pentadiene
D) (Z)-3,4-dimethyl-1,3-pentadiene
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6
Which of the following are conjugated dienes? <strong>Which of the following are conjugated dienes?  </strong> A) only 1 B) only 2 C) only 1 and 2 D) 1, 2 and 3

A) only 1
B) only 2
C) only 1 and 2
D) 1, 2 and 3
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7
Which of the following terms describes the mechanism for the addition of Br2 to butadiene?

A) electrophilic addition
B) nucleophilic addition
C) pericyclic addition
D) conjugate addition
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8
What is the kinetic product obtained from the addition of 1 mole of bromine to 1,3-butadiene?

A) 3,4-dibromo-1-butene
B) (E)-1,4-dibromo-2-butene
C) (Z)-1,4-dibromo-2-butene
D) (Z)-2,3-dibromo-2-butene
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9
Which of the following is not a major organic product obtained from the addition of 1 mole of bromine to (E)-1,3-pentadiene?

A) (E)-4,5-dibromo-2-pentene
B) 3,4-dibromo-1-pentene
C) (E)-1,4-dibromo-2-pentene
D) (E)-1,2-dibromo-2-pentene
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10
What is (are) the major organic product(s) formed in the following reaction? <strong>What is (are) the major organic product(s) formed in the following reaction?  </strong> A) only 1 B) only 1 and 2 C) only 1 and 3 D) only 2 and 4

A) only 1
B) only 1 and 2
C) only 1 and 3
D) only 2 and 4
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11
What is the reactive intermediate in the reaction of 1,3-butadiene with HBr resulting in 1,2-addition?

A) cyclic bromonium cation
B) allylic cation
C) allylic radical
D) dienophile
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12
Which of the following arrangements of p atomic orbitals gives the highest energy π-antibonding molecular orbital of 1,3-butadiene? <strong>Which of the following arrangements of p atomic orbitals gives the highest energy π-antibonding molecular orbital of 1,3-butadiene?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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13
What is the systematic IUPAC name of the following compound? <strong>What is the systematic IUPAC name of the following compound?  </strong> A) (3S,4E)-3-ethyl-3,4-dimethyl-1,4-hexadiene B) (3R,4E)-3-ethyl-3,4-dimethyl-1,4-hexadiene C) (3S,4Z)-3-ethyl-3,4-dimethyl-1,4-hexadiene D) (3R,4Z)-3-ethyl-3,4-dimethyl-1,4-hexadiene

A) (3S,4E)-3-ethyl-3,4-dimethyl-1,4-hexadiene
B) (3R,4E)-3-ethyl-3,4-dimethyl-1,4-hexadiene
C) (3S,4Z)-3-ethyl-3,4-dimethyl-1,4-hexadiene
D) (3R,4Z)-3-ethyl-3,4-dimethyl-1,4-hexadiene
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14
Which of the following arrangements of p atomic orbitals gives the lowest energy π-bonding molecular orbital of 1,3-butadiene? <strong>Which of the following arrangements of p atomic orbitals gives the lowest energy π-bonding molecular orbital of 1,3-butadiene?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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15
What is the thermodynamic product obtained from the addition of 1 mole of bromine to 1,3-butadiene?

A) 3,4-dibromo-1-butene
B) (E)-1,4-dibromo-2-butene
C) (Z)-1,4-dibromo-2-butene
D) (Z)-2,3-dibromo-2-butene
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16
What is (are) the major organic product(s) formed in the following reaction? <strong>What is (are) the major organic product(s) formed in the following reaction?  </strong> A) only 1 B) only 2 C) only 1 and 3 D) only 2 and 4

A) only 1
B) only 2
C) only 1 and 3
D) only 2 and 4
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17
Which of the following are conjugated dienes? <strong>Which of the following are conjugated dienes?  </strong> A) only 1 B) only 2 C) only 1 and 2 D) 1, 2 and 3

A) only 1
B) only 2
C) only 1 and 2
D) 1, 2 and 3
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18
What is (are) the major organic product(s) formed in the following reaction? <strong>What is (are) the major organic product(s) formed in the following reaction?  </strong> A) only 1 B) only 1 and 3 C) only 2 and 4 D) only 1 and 4

A) only 1
B) only 1 and 3
C) only 2 and 4
D) only 1 and 4
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19
Which of the following arrangements of p atomic orbitals of 1,3-butadiene has the greatest number of nodes? <strong>Which of the following arrangements of p atomic orbitals of 1,3-butadiene has the greatest number of nodes?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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20
What is the IUPAC name of the following compound? <strong>What is the IUPAC name of the following compound?  </strong> A) (R)-3-vinyl-1-butene B) 3-methyl-1,5-pentadiene C) 3-methyl-1,4-pentadiene D) (R)-3-methyl-1,4-pentadiene

A) (R)-3-vinyl-1-butene
B) 3-methyl-1,5-pentadiene
C) 3-methyl-1,4-pentadiene
D) (R)-3-methyl-1,4-pentadiene
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21
Which of the following has the highest value of λmax in the ultraviolet-visible spectrum? <strong>Which of the following has the highest value of λ<sub>max</sub> in the ultraviolet-visible spectrum?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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22
What are the units of λmax in ultraviolet-visible spectroscopy?

A) J⋅mol−1
B) M−1
C) nm
D) none, λmax is a dimensionless quantity
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23
For a diene to undergo a Diels-Alder reaction it must be able to adopt an s-trans conformation.
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24
Which of the following energy diagrams represents the electronic state of butadiene after absorption of radiation? <strong>Which of the following energy diagrams represents the electronic state of butadiene after absorption of radiation?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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25
Which of the following relationships is not valid as applied to ultraviolet-visible spectroscopy?

A) A = log (Io/I)
B) A = εcl
C) ΔE = hν
D) A = λmaxl
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26
The conjugated portion of the following molecule is circled. The conjugated portion of the following molecule is circled.
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27
Electrophilic addition reaction of conjugated dienes that occur at high temperature and/or long reaction times (reversible conditions) are said to be under kinetic control.
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28
Which of the following processes takes place upon absorption of ultraviolet-visible radiation?

A) bond vibration
B) electron excitation
C) nuclear spin flip
D) electron spin flip
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29
What range of wavelengths corresponds to the ultraviolet region of the electromagnetic spectrum?

A) 200-400 nm
B) 400-700 nm
C) 2.5-25 μm
D) 2-10 mm
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30
Which of the following has the highest value of λmax in the ultraviolet-visible spectrum? <strong>Which of the following has the highest value of λ<sub>max</sub> in the ultraviolet-visible spectrum?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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31
Which of the following reaction coordinate diagrams explains the formation of different thermodynamic (T) and kinetic products from the same reactants (R)? <strong>Which of the following reaction coordinate diagrams explains the formation of different thermodynamic (T) and kinetic products from the same reactants (R)?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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32
Consider the following structure. Consider the following structure.   This substance could be produced by the reaction of the following diene and dienophile.  This substance could be produced by the reaction of the following diene and dienophile. Consider the following structure.   This substance could be produced by the reaction of the following diene and dienophile.
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33
The conjugated portion of the following molecule is circled. The conjugated portion of the following molecule is circled.
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34
Which of the following energy diagrams represents the electronic state of the ground state of 1,3-butadiene? <strong>Which of the following energy diagrams represents the electronic state of the ground state of 1,3-butadiene?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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35
What are the units of ε in ultraviolet-visible spectroscopy?

A) M−1⋅cm−1
B) M⋅cm
C) J⋅mol−1⋅M−1
D) none, ε is a dimensionless quantity
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36
What quantity is abbreviated as ε in ultraviolet-visible spectroscopy?

A) absorbance
B) molecular absorptivity
C) intensity of transmitted light
D) wavelength of maximum absorbance
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37
Which of the following laws relates absorbance to the concentration of a sample and the pathlength in ultraviolet-visible spectroscopy?

A) Buzz-Beer law
B) Beer-Lambert law
C) Duff-Beer law
D) Christopher-Lambert law
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38
Which of the following electronic transitions is apparent in the ultraviolet-visible spectrum of 1,3-butadiene?

A) n → π*
B) π → π *
C) σ → π *
D) σ → π
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39
What is (are) the major organic product(s) formed in the following reaction? <strong>What is (are) the major organic product(s) formed in the following reaction?  </strong> A) only 1 B) only 2 C) only 3 D) 1, 2 and 3

A) only 1
B) only 2
C) only 3
D) 1, 2 and 3
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40
What are the units of absorbance, A, in ultraviolet-visible spectroscopy?

A) J⋅mol−1
B) nm⋅mol−1
C) J⋅mol−1⋅M−1
D) none, A is a dimensionless quantity
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41
Consider the following reaction. Consider the following reaction.   This is an example of a sigmatropic reaction with a [3,3]-shift. This is an example of a sigmatropic reaction with a [3,3]-shift.
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42
Consider the reaction below to answer the following question(s). Consider the reaction below to answer the following question(s).   Fill in the blank in the question with the appropriate letter. The dienophile in the reaction is ____. Fill in the blank in the question with the appropriate letter.
The dienophile in the reaction is ____.
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43
The following spectrum could arise from π to π* transitions. The following spectrum could arise from π to π* transitions.
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44
Consider the reaction below to answer the following question(s): Consider the reaction below to answer the following question(s):   Enter the appropriate letter in the blank for each the following statements. The product that results from following mechanistic step is _____.  Enter the appropriate letter in the blank for each the following statements.
The product that results from following mechanistic step is _____. Consider the reaction below to answer the following question(s):   Enter the appropriate letter in the blank for each the following statements. The product that results from following mechanistic step is _____.
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45
Consider the reaction below to answer the following question(s). Consider the reaction below to answer the following question(s).   Fill in the blank in the question with the appropriate letter. This is an example of a(n) ____________ reaction. A. sigmatropic reaction B. electrophillic addition C. Diels-Alder reaction D. Cope rearrangement Fill in the blank in the question with the appropriate letter.
This is an example of a(n) ____________ reaction.
A. sigmatropic reaction
B. electrophillic addition
C. Diels-Alder reaction
D. Cope rearrangement
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46
What is the IUPAC name of the following compound? What is the IUPAC name of the following compound?
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47
What is the IUPAC name of the following compound? What is the IUPAC name of the following compound?
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48
Consider the following spectrum for a conjugated diene. Consider the following spectrum for a conjugated diene.   If a similar spectrum were taken for a conjugated tetraene, the λ<sub>max</sub> would be _________than 217 nm. If a similar spectrum were taken for a conjugated tetraene, the λmax would be _________than 217 nm.
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49
Based on the following table.
Based on the following table.   Compound ______ has the largest energy difference between the HOMO and LUMO.
Compound ______ has the largest energy difference between the HOMO and LUMO.
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50
The following compound could act as a diene in a Diels-Alder reaction. The following compound could act as a diene in a Diels-Alder reaction.
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51
Sigmatropic shifts, cycloaddition reactions and anuulation reactions are all examples of pericyclic reactions.
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52
The following two compounds could be easily distinguished by NMR, IR, UV or MS spectra. The following two compounds could be easily distinguished by NMR, IR, UV or MS spectra.
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53
Consider the following reaction. Consider the following reaction.   This is an example of a sigmatropic reaction with a [3,3]-shift. This is an example of a sigmatropic reaction with a [3,3]-shift.
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54
For Diels-Alder cycloaddition reactions to take place most rapidly and in highest yield a dienophile must be substituted with electron-donating groups.
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55
Consider the reaction below to answer the following question(s): Consider the reaction below to answer the following question(s):   Enter the appropriate letter in the blank for each the following statements. The electrophile in this reaction is ____. Enter the appropriate letter in the blank for each the following statements.
The electrophile in this reaction is ____.
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56
Consider the reaction below to answer the following question(s). Consider the reaction below to answer the following question(s).   Fill in the blank in the question with the appropriate letter. The diene in the reaction is ____. Fill in the blank in the question with the appropriate letter.
The diene in the reaction is ____.
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57
Consider the reaction below to answer the following question(s): Consider the reaction below to answer the following question(s):   Enter the appropriate letter in the blank for each the following statements. The nucleophile in this reaction is ____. Enter the appropriate letter in the blank for each the following statements.
The nucleophile in this reaction is ____.
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58
Consider the reaction below to answer the following question(s): Consider the reaction below to answer the following question(s):   Enter the appropriate letter in the blank for each the following statements. The product that results from 1,4-addition is _____. Enter the appropriate letter in the blank for each the following statements.
The product that results from 1,4-addition is _____.
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59
Consider the reaction below to answer the following question(s): Consider the reaction below to answer the following question(s):   Enter the appropriate letter in the blank for each the following statements. The kinetically controlled product in this reaction is _____. Enter the appropriate letter in the blank for each the following statements.
The kinetically controlled product in this reaction is _____.
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60
When an organic molecule is irradiated with ultraviolet radiation, the energy absorbed by the molecule corresponds to the amount necessary to excite electrons from one molecular orbital to another.
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61
Provide the structures of the constitutional isomers of the two major organic products obtained from the following reaction? Provide the structures of the constitutional isomers of the two major organic products obtained from the following reaction?
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62
What are the two major organic products obtained from the following reaction? What are the two major organic products obtained from the following reaction?
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63
Why carbonyl groups of aldehydes and ketones on conjugation with carbon-carbon double bonds show strong absorption in the ultraviolet spectrum?
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64
The molar absorptivity of ethylene in hexane is 15,000 L mol−1 cm−1. What is the maximum absorbance observed at a concentration of 1.5 x 10−4 mol L−1? (Path length = 1 cm)

A) 2.25
B) 1.25
C) 3.25
D) 2.52
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65
Which of 1,3-cyclohexadiene and 1,4-cyclohexadiene has the greatest heat of hydrogenation (i.e., the most exothermic reaction with H2 in the presence of a catalyst). Provide a brief explanation for your choice ?
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66
What is the major organic product obtained from the following reaction? What is the major organic product obtained from the following reaction?
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67
The [2+2] cycloaddition reaction of ethylene to form cyclobutane does not occur because _____. ​ <strong>The [2+2] cycloaddition reaction of ethylene to form cyclobutane does not occur because _____. ​  </strong> A) the reaction is forbidden as determined by the frontier molecular orbital analysis B) the reaction is allowed as determined by the frontier molecular orbital analysis C) the reaction is allowed, and ethylene collides in a suprafacial manner D) the reaction is allowed, and ethylene collides in an antarafacial manner

A) the reaction is forbidden as determined by the frontier molecular orbital analysis
B) the reaction is allowed as determined by the frontier molecular orbital analysis
C) the reaction is allowed, and ethylene collides in a suprafacial manner
D) the reaction is allowed, and ethylene collides in an antarafacial manner
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68
How would you be able to distinguish between 1,3-cyclohexadiene and 1,4-cyclohexadiene using ultraviolet spectroscopy?
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69
What are the two major organic products obtained from the following reaction? What are the two major organic products obtained from the following reaction?
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70
Draw two resonance structures of the reactive intermediate that accounts for the formation of 1,2- and 1,4-addition products upon reaction of 1,3-butadiene with one equivalent of HBr.
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71
Pericyclic reactions occur in a single step with the _____.

A) formation of a radical
B) formation of an ionic intermediate
C) formation of a molecular ion
D) formation of a transition state
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72
Identify the product of the given reaction. ​ <strong>Identify the product of the given reaction. ​  </strong> A) I B) II C) IV D) III

A) I
B) II
C) IV
D) III
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73
Identify the product of the given reaction. ​ <strong>Identify the product of the given reaction. ​  </strong> A) I B) II C) IV D) III

A) I
B) II
C) IV
D) III
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74
Draw two resonance structures of the reactive intermediate that accounts for the formation of 1,2- and 1,4-addition products upon reaction of 1,3-butadiene with one equivalent of bromine.
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75
A reaction in which two reactants add together in a single step to form a cyclic product is known as a _____.

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