Deck 14: Conjugated Compounds and Ultraviolet Spectroscopy

Full screen (f)
exit full mode
Question
Name: Name:  <div style=padding-top: 35px>
Use Space or
up arrow
down arrow
to flip the card.
Question
Exhibit 14-2
Consider the reaction below to answer the following question(s): 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.<div style=padding-top: 35px>
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.
Question
Exhibit 14-2
Consider the reaction below to answer the following question(s): 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 _____.<div style=padding-top: 35px>
Refer to Exhibit 14-2.The product that results from 1,4-addition is _____.
Question
Name: Name:  <div style=padding-top: 35px>
Question
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
Question
Exhibit 14-2
Consider the reaction below to answer the following question(s): Exhibit 14-2 Consider the reaction below to answer the following question(s):   Refer to Exhibit 14-2.The electrophile in this reaction is ____.<div style=padding-top: 35px>
Refer to Exhibit 14-2.The electrophile in this reaction is ____.
Question
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
Question
Draw: 2-methyl-1,3-butadiene
Question
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
Question
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
Question
Which of the following compounds will react as a diene in a Diels-Alder reaction?

A) <strong>Which of the following compounds will react as a diene in a Diels-Alder reaction?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Which of the following compounds will react as a diene in a Diels-Alder reaction?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which of the following compounds will react as a diene in a Diels-Alder reaction?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which of the following compounds will react as a diene in a Diels-Alder reaction?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
Exhibit 14-2
Consider the reaction below to answer the following question(s): Exhibit 14-2 Consider the reaction below to answer the following question(s):   Refer to Exhibit 14-2.The nucleophile in this reaction is ____.<div style=padding-top: 35px>
Refer to Exhibit 14-2.The nucleophile in this reaction is ____.
Question
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
Question
Exhibit 14-2
Consider the reaction below to answer the following question(s): 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 _____.<div style=padding-top: 35px>
Refer to Exhibit 14-2.The kinetically controlled product in this reaction is _____.
Question
Draw: (2Z,4Z)-hexadiene
Question
Which of the following compounds would show the longest wavelength λmax in its UV spectrum?

A) <strong>Which of the following compounds would show the longest wavelength λ<sub>max</sub> in its UV spectrum?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Which of the following compounds would show the longest wavelength λ<sub>max</sub> in its UV spectrum?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which of the following compounds would show the longest wavelength λ<sub>max</sub> in its UV spectrum?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which of the following compounds would show the longest wavelength λ<sub>max</sub> in its UV spectrum?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
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
Question
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*
Question
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
Question
Exhibit 14-2
Consider the reaction below to answer the following question(s): 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.<div style=padding-top: 35px>
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.
Question
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.
Question
​What would be the stereochemistry of the product of the following reaction? ​What would be the stereochemistry of the product of the following reaction?   ​<div style=padding-top: 35px>
Question
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
Question
Draw the skeletal formulas for the product of the reaction of the following with HBr. Draw the skeletal formulas for the product of the reaction of the following with HBr.  <div style=padding-top: 35px>
Question
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 <strong>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?</strong> A)QT7 B)XR4 C)B78 D)L99 <div style=padding-top: 35px> 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
Question
Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λmax? <strong>Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λ<sub>max</sub>?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A) <strong>Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λ<sub>max</sub>?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λ<sub>max</sub>?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λ<sub>max</sub>?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λ<sub>max</sub>?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λ<sub>max</sub>?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
​Draw the mechanism of the Diels-Alder reaction between propenal and 2-methyl-1,3-butadiene.
Question
Exhibit 14-7
Consider the reaction below to answer the following question(s). <strong>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.</strong> A)Woodward-Hoffman B)conjugate addition C)Diels-Alder D)electrophilic addition <div style=padding-top: 35px>
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
Question
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) <strong>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?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>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?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>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?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>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?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
Which of the following arises from π to π* transitions?

A) <strong>Which of the following arises from π to π* transitions?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which of the following arises from π to π* transitions?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which of the following arises from π to π* transitions?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which of the following arises from π to π* transitions?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which of the following arises from π to π* transitions?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
​Draw the mechanism of the bromination of 2-ethyl-1,3-pentadiene.
Question
​The unit for molar absorptivity is:

A)​L/cm
B)​(L .mol)/cm
C)​L/(mol .cm)
D)​mol/L
Question
​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.
Question
​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
Question
Consider the following spectrum for a conjugated diene. <strong>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:</strong> A)close to 217 nm B)less than 217 nm C)greater than 217 nm <div style=padding-top: 35px> 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
Question
​Draw the mechanism of the bromination of 1,3-pentadiene and indicate the major and minor products.
Question
Which of the following has the highest degree of conjugation? Atoms other than carbon and hydrogen are labeled.

A) <strong>Which of the following has the highest degree of conjugation? Atoms other than carbon and hydrogen are labeled.</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Which of the following has the highest degree of conjugation? Atoms other than carbon and hydrogen are labeled.</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which of the following has the highest degree of conjugation? Atoms other than carbon and hydrogen are labeled.</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which of the following has the highest degree of conjugation? Atoms other than carbon and hydrogen are labeled.</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
Exhibit 14-7
Consider the reaction below to answer the following question(s). Exhibit 14-7 Consider the reaction below to answer the following question(s).   Refer to Exhibit 14-7.The diene in the reaction is ____.<div style=padding-top: 35px>
Refer to Exhibit 14-7.The diene in the reaction is ____.
Question
​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 <strong>​Which of the following is the most likely to happen when a conjugated diene is irradiated with ultraviolet light?</strong> 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. <div style=padding-top: 35px> electron is promoted from the highest occupied molecular orbital to the lowest unoccupied molecular orbital.
C)​A <strong>​Which of the following is the most likely to happen when a conjugated diene is irradiated with ultraviolet light?</strong> 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. <div style=padding-top: 35px> 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.
Question
Exhibit 14-7
Consider the reaction below to answer the following question(s). Exhibit 14-7 Consider the reaction below to answer the following question(s).   Refer to Exhibit 14-7.The dienophile in the reaction is ____.<div style=padding-top: 35px>
Refer to Exhibit 14-7.The dienophile in the reaction is ____.
Unlock Deck
Sign up to unlock the cards in this deck!
Unlock Deck
Unlock Deck
1/40
auto play flashcards
Play
simple tutorial
Full screen (f)
exit full mode
Deck 14: Conjugated Compounds and Ultraviolet Spectroscopy
1
Name: Name:
2,3,4,5-tetramethyl-2,4-hexadiene
2
Exhibit 14-2
Consider the reaction below to answer the following question(s): 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.
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): 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 _____.
Refer to Exhibit 14-2.The product that results from 1,4-addition is _____.
C
4
Name: Name:
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
6
Exhibit 14-2
Consider the reaction below to answer the following question(s): Exhibit 14-2 Consider the reaction below to answer the following question(s):   Refer to Exhibit 14-2.The electrophile in this reaction is ____.
Refer to Exhibit 14-2.The electrophile in this reaction is ____.
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
8
Draw: 2-methyl-1,3-butadiene
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
11
Which of the following compounds will react as a diene in a Diels-Alder reaction?

A) <strong>Which of the following compounds will react as a diene in a Diels-Alder reaction?</strong> A)   B)   C)   D)
B) <strong>Which of the following compounds will react as a diene in a Diels-Alder reaction?</strong> A)   B)   C)   D)
C) <strong>Which of the following compounds will react as a diene in a Diels-Alder reaction?</strong> A)   B)   C)   D)
D) <strong>Which of the following compounds will react as a diene in a Diels-Alder reaction?</strong> A)   B)   C)   D)
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
12
Exhibit 14-2
Consider the reaction below to answer the following question(s): Exhibit 14-2 Consider the reaction below to answer the following question(s):   Refer to Exhibit 14-2.The nucleophile in this reaction is ____.
Refer to Exhibit 14-2.The nucleophile in this reaction is ____.
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
14
Exhibit 14-2
Consider the reaction below to answer the following question(s): 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 _____.
Refer to Exhibit 14-2.The kinetically controlled product in this reaction is _____.
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
15
Draw: (2Z,4Z)-hexadiene
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
16
Which of the following compounds would show the longest wavelength λmax in its UV spectrum?

A) <strong>Which of the following compounds would show the longest wavelength λ<sub>max</sub> in its UV spectrum?</strong> A)   B)   C)   D)
B) <strong>Which of the following compounds would show the longest wavelength λ<sub>max</sub> in its UV spectrum?</strong> A)   B)   C)   D)
C) <strong>Which of the following compounds would show the longest wavelength λ<sub>max</sub> in its UV spectrum?</strong> A)   B)   C)   D)
D) <strong>Which of the following compounds would show the longest wavelength λ<sub>max</sub> in its UV spectrum?</strong> A)   B)   C)   D)
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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*
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
20
Exhibit 14-2
Consider the reaction below to answer the following question(s): 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.
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.
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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.
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
22
​What would be the stereochemistry of the product of the following reaction? ​What would be the stereochemistry of the product of the following reaction?   ​
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
24
Draw the skeletal formulas for the product of the reaction of the following with HBr. Draw the skeletal formulas for the product of the reaction of the following with HBr.
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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 <strong>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?</strong> A)QT7 B)XR4 C)B78 D)L99 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
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
26
Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λmax? <strong>Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λ<sub>max</sub>?  </strong> A)   B)   C)   D)   E)

A) <strong>Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λ<sub>max</sub>?  </strong> A)   B)   C)   D)   E)
B) <strong>Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λ<sub>max</sub>?  </strong> A)   B)   C)   D)   E)
C) <strong>Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λ<sub>max</sub>?  </strong> A)   B)   C)   D)   E)
D) <strong>Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λ<sub>max</sub>?  </strong> A)   B)   C)   D)   E)
E) <strong>Based on the following spectrum,what is the energy in kilojoules per mole of photons that corresponds to the λ<sub>max</sub>?  </strong> A)   B)   C)   D)   E)
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
27
​Draw the mechanism of the Diels-Alder reaction between propenal and 2-methyl-1,3-butadiene.
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
28
Exhibit 14-7
Consider the reaction below to answer the following question(s). <strong>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.</strong> A)Woodward-Hoffman B)conjugate addition C)Diels-Alder D)electrophilic addition
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
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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) <strong>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?</strong> A)   B)   C)   D)
B) <strong>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?</strong> A)   B)   C)   D)
C) <strong>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?</strong> A)   B)   C)   D)
D) <strong>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?</strong> A)   B)   C)   D)
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
30
Which of the following arises from π to π* transitions?

A) <strong>Which of the following arises from π to π* transitions?</strong> A)   B)   C)   D)   E)
B) <strong>Which of the following arises from π to π* transitions?</strong> A)   B)   C)   D)   E)
C) <strong>Which of the following arises from π to π* transitions?</strong> A)   B)   C)   D)   E)
D) <strong>Which of the following arises from π to π* transitions?</strong> A)   B)   C)   D)   E)
E) <strong>Which of the following arises from π to π* transitions?</strong> A)   B)   C)   D)   E)
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
31
​Draw the mechanism of the bromination of 2-ethyl-1,3-pentadiene.
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
32
​The unit for molar absorptivity is:

A)​L/cm
B)​(L .mol)/cm
C)​L/(mol .cm)
D)​mol/L
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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.
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
35
Consider the following spectrum for a conjugated diene. <strong>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:</strong> 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
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
36
​Draw the mechanism of the bromination of 1,3-pentadiene and indicate the major and minor products.
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
37
Which of the following has the highest degree of conjugation? Atoms other than carbon and hydrogen are labeled.

A) <strong>Which of the following has the highest degree of conjugation? Atoms other than carbon and hydrogen are labeled.</strong> A)   B)   C)   D)
B) <strong>Which of the following has the highest degree of conjugation? Atoms other than carbon and hydrogen are labeled.</strong> A)   B)   C)   D)
C) <strong>Which of the following has the highest degree of conjugation? Atoms other than carbon and hydrogen are labeled.</strong> A)   B)   C)   D)
D) <strong>Which of the following has the highest degree of conjugation? Atoms other than carbon and hydrogen are labeled.</strong> A)   B)   C)   D)
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
38
Exhibit 14-7
Consider the reaction below to answer the following question(s). Exhibit 14-7 Consider the reaction below to answer the following question(s).   Refer to Exhibit 14-7.The diene in the reaction is ____.
Refer to Exhibit 14-7.The diene in the reaction is ____.
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
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 <strong>​Which of the following is the most likely to happen when a conjugated diene is irradiated with ultraviolet light?</strong> 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. electron is promoted from the highest occupied molecular orbital to the lowest unoccupied molecular orbital.
C)​A <strong>​Which of the following is the most likely to happen when a conjugated diene is irradiated with ultraviolet light?</strong> 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. 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.
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
40
Exhibit 14-7
Consider the reaction below to answer the following question(s). Exhibit 14-7 Consider the reaction below to answer the following question(s).   Refer to Exhibit 14-7.The dienophile in the reaction is ____.
Refer to Exhibit 14-7.The dienophile in the reaction is ____.
Unlock Deck
Unlock for access to all 40 flashcards in this deck.
Unlock Deck
k this deck
locked card icon
Unlock Deck
Unlock for access to all 40 flashcards in this deck.