Deck 14: Conjugated Compounds and Ultraviolet Spectroscopy
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Deck 14: Conjugated Compounds and Ultraviolet Spectroscopy
1
Name: 

2,3,4,5-tetramethyl-2,4-hexadiene
2
Exhibit 14-2
Consider the reaction below to answer the following question(s):
Refer to Exhibit 14-2.This reaction shows the preferred electrophilic addition of HBr to this unsymmetrical alkene.Draw the products of electrophilic addition to the opposite end of the conjugated diene.
Consider the reaction below to answer the following question(s):

Refer to Exhibit 14-2.This reaction shows the preferred electrophilic addition of HBr to this unsymmetrical alkene.Draw the products of electrophilic addition to the opposite end of the conjugated diene.

3
Exhibit 14-2
Consider the reaction below to answer the following question(s):
Refer to Exhibit 14-2.The product that results from 1,4-addition is _____.
Consider the reaction below to answer the following question(s):

Refer to Exhibit 14-2.The product that results from 1,4-addition is _____.
C
4
Name: 

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5
When an organic molecule is irradiated with ultraviolet radiation,the energy absorbed by the molecule corresponds to:
A)the amount necessary to increase molecular motions in functional groups
B)the amount necessary to excite electrons from one molecular orbital to another
C)the amount necessary to "flip" the spin of atomic nuclei
D)the amount necessary to strip a molecule of one electron to generate a radical cation
A)the amount necessary to increase molecular motions in functional groups
B)the amount necessary to excite electrons from one molecular orbital to another
C)the amount necessary to "flip" the spin of atomic nuclei
D)the amount necessary to strip a molecule of one electron to generate a radical cation
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6
Exhibit 14-2
Consider the reaction below to answer the following question(s):
Refer to Exhibit 14-2.The electrophile in this reaction is ____.
Consider the reaction below to answer the following question(s):

Refer to Exhibit 14-2.The electrophile in this reaction is ____.
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7
For a diene to undergo a Diels-Alder reaction it must:
A)be substituted with electron-withdrawing groups
B)be able to adopt an s-trans conformation
C)be substituted with electron-donating groups
D)be able to adopt an s-cis conformation
A)be substituted with electron-withdrawing groups
B)be able to adopt an s-trans conformation
C)be substituted with electron-donating groups
D)be able to adopt an s-cis conformation
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8
Draw: 2-methyl-1,3-butadiene
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9
The amount of energy in electromagnetic radiation is related to the frequency and wavelength of the radiation.High energy radiation like gamma rays is of:
A)low frequency and short wavelength
B)low frequency and long wavelength
C)high frequency and short wavelength
D)high frequency and long wavelength
A)low frequency and short wavelength
B)low frequency and long wavelength
C)high frequency and short wavelength
D)high frequency and long wavelength
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10
2-Chloro-1,3-butadiene is polymerized to yield an excellent,expensive synthetic rubber with good weather resistance called:
A)diprene
B)isoprene
C)styrene
D)neoprene
A)diprene
B)isoprene
C)styrene
D)neoprene
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11
Which of the following compounds will react as a diene in a Diels-Alder reaction?
A)
B)
C)
D)
A)

B)

C)

D)

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12
Exhibit 14-2
Consider the reaction below to answer the following question(s):
Refer to Exhibit 14-2.The nucleophile in this reaction is ____.
Consider the reaction below to answer the following question(s):

Refer to Exhibit 14-2.The nucleophile in this reaction is ____.
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13
Electrophilic addition reaction of conjugated dienes that occur at high temperature and/or long reaction times (reversible conditions) are said to be under:
A)1,2-control
B)kinetic control
C)1,4-control
D)thermodynamic control
A)1,2-control
B)kinetic control
C)1,4-control
D)thermodynamic control
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14
Exhibit 14-2
Consider the reaction below to answer the following question(s):
Refer to Exhibit 14-2.The kinetically controlled product in this reaction is _____.
Consider the reaction below to answer the following question(s):

Refer to Exhibit 14-2.The kinetically controlled product in this reaction is _____.
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15
Draw: (2Z,4Z)-hexadiene
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16
Which of the following compounds would show the longest wavelength λmax in its UV spectrum?
A)
B)
C)
D)
A)

B)

C)

D)

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17
In 1839,Charles Goodyear discovered a process by which both natural and synthetic rubbers are hardened.This process is called:
A)diazotization
B)vulcanization
C)polymerization
D)condensation
A)diazotization
B)vulcanization
C)polymerization
D)condensation
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18
A physical constant that is the quantitative measure of the amount of UV light absorbed by a compound.
A)A
B)ε
C)λmax
D)π*
A)A
B)ε
C)λmax
D)π*
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19
For Diels-Alder cycloaddition reactions to take place most rapidly and in highest yield the dienophile must:
A)be substituted with electron-withdrawing groups
B)be able to adopt an s-trans conformation
C)be substituted with electron-donating groups
D)be able to adopt an s-cis conformation
A)be substituted with electron-withdrawing groups
B)be able to adopt an s-trans conformation
C)be substituted with electron-donating groups
D)be able to adopt an s-cis conformation
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20
Exhibit 14-2
Consider the reaction below to answer the following question(s):
Refer to Exhibit 14-2.Write a stepwise mechanism that accounts for both of the products shown.Show all intermediate structures and electron flow with arrows.
Consider the reaction below to answer the following question(s):

Refer to Exhibit 14-2.Write a stepwise mechanism that accounts for both of the products shown.Show all intermediate structures and electron flow with arrows.
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21
If ΔH°hydrog for a monosubstituted alkene is 126 kJ/mol,which of the following systems is most likely to be a conjugated system?
A)3 double bonds,ΔH°hydrog = 379 kJ/mol
B)2 double bond,ΔH°hydrog = 254 kJ/mol
C)4 double bonds,ΔH°hydrog = 505 kJ/mol
D)None of these are likely to be conjugated.
A)3 double bonds,ΔH°hydrog = 379 kJ/mol
B)2 double bond,ΔH°hydrog = 254 kJ/mol
C)4 double bonds,ΔH°hydrog = 505 kJ/mol
D)None of these are likely to be conjugated.
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22
What would be the stereochemistry of the product of the following reaction?
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23
Based on the following table,in which compound is the energy difference between the HOMO and LUMO the largest? Compound
Λmax (nm)
W
190
X
340
Y
560
Z
250
A)W
B)X
C)Y
D)Z
Λmax (nm)
W
190
X
340
Y
560
Z
250
A)W
B)X
C)Y
D)Z
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24
Draw the skeletal formulas for the product of the reaction of the following with HBr. 

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25
Consider the following data for a series of hypothetical plant pigments. Pigment
Ε
QT7
15,300
XR4
41,000
B78
30,800
L99
10,600
The Absorbance of a
solution containing one of these pigments,measured in a 1.00 cm cell,was 0.345.Which pigment was in the solution?
A)QT7
B)XR4
C)B78
D)L99
Ε
QT7
15,300
XR4
41,000
B78
30,800
L99
10,600
The Absorbance of a
solution containing one of these pigments,measured in a 1.00 cm cell,was 0.345.Which pigment was in the solution?A)QT7
B)XR4
C)B78
D)L99
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26
Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λmax? 
A)
B)
C)
D)
E)

A)

B)

C)

D)

E)

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27
Draw the mechanism of the Diels-Alder reaction between propenal and 2-methyl-1,3-butadiene.
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28
Exhibit 14-7
Consider the reaction below to answer the following question(s).
Refer to Exhibit 14-7.This is an example of a(n) ____________ reaction.
A)Woodward-Hoffman
B)conjugate addition
C)Diels-Alder
D)electrophilic addition
Consider the reaction below to answer the following question(s).

Refer to Exhibit 14-7.This is an example of a(n) ____________ reaction.
A)Woodward-Hoffman
B)conjugate addition
C)Diels-Alder
D)electrophilic addition
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29
What is the concentration of a solution of a plant pigment (ε = 37,500) if an Absorbance of 0.751 were obtained in a cell with a 5.00 cm path length?
A)
B)
C)
D)
A)

B)

C)

D)

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30
Which of the following arises from π to π* transitions?
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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31
Draw the mechanism of the bromination of 2-ethyl-1,3-pentadiene.
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32
The unit for molar absorptivity is:
A)L/cm
B)(L .mol)/cm
C)L/(mol .cm)
D)mol/L
A)L/cm
B)(L .mol)/cm
C)L/(mol .cm)
D)mol/L
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33
Calculate the concentration of β-carotene in a sample which is placed in a cell with a pathlength of 1.0 cm and the UV absorbance reads 0.56.The molar absorbtivity of β-carotene is found to be 138,000 L mol-1 cm-1.
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34
Which of the following compounds is the most stable?
A)penta-2,3-diene
B)2,4-hexadiene
C)1,4-pentadiene
D)3,6-octadiene
A)penta-2,3-diene
B)2,4-hexadiene
C)1,4-pentadiene
D)3,6-octadiene
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35
Consider the following spectrum for a conjugated diene.
If a similar spectrum were taken for a conjugated tetraene,the λmax would be:
A)close to 217 nm
B)less than 217 nm
C)greater than 217 nm
If a similar spectrum were taken for a conjugated tetraene,the λmax would be:A)close to 217 nm
B)less than 217 nm
C)greater than 217 nm
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36
Draw the mechanism of the bromination of 1,3-pentadiene and indicate the major and minor products.
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37
Which of the following has the highest degree of conjugation? Atoms other than carbon and hydrogen are labeled.
A)
B)
C)
D)
A)

B)

C)

D)

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38
Exhibit 14-7
Consider the reaction below to answer the following question(s).
Refer to Exhibit 14-7.The diene in the reaction is ____.
Consider the reaction below to answer the following question(s).

Refer to Exhibit 14-7.The diene in the reaction is ____.
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39
Which of the following is the most likely to happen when a conjugated diene is irradiated with ultraviolet light?
A)The bonds between different atoms in the molecule undergo symmetric stretching.
B)A
electron is promoted from the highest occupied molecular orbital to the lowest unoccupied molecular orbital.
C)A
electron is demoted from the lowest occupied molecular orbital to the highest unoccupied molecular orbital.
D)The bonds between different atoms in the molecule undergo asymmetric stretching.
A)The bonds between different atoms in the molecule undergo symmetric stretching.
B)A
electron is promoted from the highest occupied molecular orbital to the lowest unoccupied molecular orbital.C)A
electron is demoted from the lowest occupied molecular orbital to the highest unoccupied molecular orbital.D)The bonds between different atoms in the molecule undergo asymmetric stretching.
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40
Exhibit 14-7
Consider the reaction below to answer the following question(s).
Refer to Exhibit 14-7.The dienophile in the reaction is ____.
Consider the reaction below to answer the following question(s).

Refer to Exhibit 14-7.The dienophile in the reaction is ____.
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