Deck 27: Synthetic Polymers
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Deck 27: Synthetic Polymers
1
Which of the following addition polymers results from the reaction below? nCF2
CF2
?
A)[
CF-CF
]n
B)[CF3-CF3]n
C)[-CF2-CH
CHCF2-]n
D)[-CF2-CF2-]n
E)[-CF2
CF2-]n
![<strong>Which of the following addition polymers results from the reaction below? nCF<sub>2</sub> <sub> </sub> CF<sub>2 </sub> <sub> </sub> ?</strong> A)[ CF-CF ]<sub>n</sub> B)[CF<sub>3</sub>-CF<sub>3</sub>]<sub>n</sub> C)[-CF<sub>2</sub>-CH CHCF<sub>2</sub>-]<sub>n</sub> D)[-CF<sub>2</sub>-CF<sub>2</sub>-]<sub>n</sub> E)[-CF<sub>2</sub> <sub> </sub> CF<sub>2</sub>-]<sub>n</sub>](https://storage.examlex.com/TB1831/11ea8a1c_2db3_6426_b657_6bcecbfae464_TB1831_11.jpg)
![<strong>Which of the following addition polymers results from the reaction below? nCF<sub>2</sub> <sub> </sub> CF<sub>2 </sub> <sub> </sub> ?</strong> A)[ CF-CF ]<sub>n</sub> B)[CF<sub>3</sub>-CF<sub>3</sub>]<sub>n</sub> C)[-CF<sub>2</sub>-CH CHCF<sub>2</sub>-]<sub>n</sub> D)[-CF<sub>2</sub>-CF<sub>2</sub>-]<sub>n</sub> E)[-CF<sub>2</sub> <sub> </sub> CF<sub>2</sub>-]<sub>n</sub>](https://storage.examlex.com/TB1831/11ea8a1c_2db3_6427_b657_c10f968857e3_TB1831_11.jpg)
A)[
![<strong>Which of the following addition polymers results from the reaction below? nCF<sub>2</sub> <sub> </sub> CF<sub>2 </sub> <sub> </sub> ?</strong> A)[ CF-CF ]<sub>n</sub> B)[CF<sub>3</sub>-CF<sub>3</sub>]<sub>n</sub> C)[-CF<sub>2</sub>-CH CHCF<sub>2</sub>-]<sub>n</sub> D)[-CF<sub>2</sub>-CF<sub>2</sub>-]<sub>n</sub> E)[-CF<sub>2</sub> <sub> </sub> CF<sub>2</sub>-]<sub>n</sub>](https://storage.examlex.com/TB1831/11ea8a1c_2db3_8b38_b657_dd9aba5ddc0e_TB1831_11.jpg)
![<strong>Which of the following addition polymers results from the reaction below? nCF<sub>2</sub> <sub> </sub> CF<sub>2 </sub> <sub> </sub> ?</strong> A)[ CF-CF ]<sub>n</sub> B)[CF<sub>3</sub>-CF<sub>3</sub>]<sub>n</sub> C)[-CF<sub>2</sub>-CH CHCF<sub>2</sub>-]<sub>n</sub> D)[-CF<sub>2</sub>-CF<sub>2</sub>-]<sub>n</sub> E)[-CF<sub>2</sub> <sub> </sub> CF<sub>2</sub>-]<sub>n</sub>](https://storage.examlex.com/TB1831/11ea8a1c_2db3_8b39_b657_59bd47563326_TB1831_11.jpg)
B)[CF3-CF3]n
C)[-CF2-CH
![<strong>Which of the following addition polymers results from the reaction below? nCF<sub>2</sub> <sub> </sub> CF<sub>2 </sub> <sub> </sub> ?</strong> A)[ CF-CF ]<sub>n</sub> B)[CF<sub>3</sub>-CF<sub>3</sub>]<sub>n</sub> C)[-CF<sub>2</sub>-CH CHCF<sub>2</sub>-]<sub>n</sub> D)[-CF<sub>2</sub>-CF<sub>2</sub>-]<sub>n</sub> E)[-CF<sub>2</sub> <sub> </sub> CF<sub>2</sub>-]<sub>n</sub>](https://storage.examlex.com/TB1831/11ea8a1c_2db3_b24a_b657_03ada4072b50_TB1831_11.jpg)
D)[-CF2-CF2-]n
E)[-CF2
![<strong>Which of the following addition polymers results from the reaction below? nCF<sub>2</sub> <sub> </sub> CF<sub>2 </sub> <sub> </sub> ?</strong> A)[ CF-CF ]<sub>n</sub> B)[CF<sub>3</sub>-CF<sub>3</sub>]<sub>n</sub> C)[-CF<sub>2</sub>-CH CHCF<sub>2</sub>-]<sub>n</sub> D)[-CF<sub>2</sub>-CF<sub>2</sub>-]<sub>n</sub> E)[-CF<sub>2</sub> <sub> </sub> CF<sub>2</sub>-]<sub>n</sub>](https://storage.examlex.com/TB1831/11ea8a1c_2db3_b24b_b657_23be445a643b_TB1831_11.jpg)
[-CF2-CF2-]n
2
Which of the following monomers has the greatest ability to undergo cationic polymerization? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
III
3
List the two major classes of synthetic polymers and give one example of each.
a)Addition polymers,also known as chain-growth polymers; polystyrene for example. b)Condensation polymers,also known as step-growth polymers; nylon for example.
4
Which of the following is the first chain propagating step in the radical polymerization of ethylene?
A)ROOR + CH2
CH2 → ROCH2CH2OR
B)∙ RO∙ + CH2
CH2 → ROCH2CH2
C)RO∙ + CH2
CH2 → ROCH
CH2 + H∙
D)∙ ∙ ROOR + CH2
CH2 → 2 ROH + CH
CH
E)∙ ∙ 2RO∙ + CH2
CH2 → 2 ROH + CH
CH
A)ROOR + CH2

B)∙ RO∙ + CH2

C)RO∙ + CH2


D)∙ ∙ ROOR + CH2


E)∙ ∙ 2RO∙ + CH2


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5
Which of the following is the chain-initiating step in the cationic polymerization of propene? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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6
Which of the following is a possible step to terminate a chain in the radical polymerization of ethylene?
A)ROOR + CH2
CH2 → ROCH2CH2OR
B)CH2
CH2 + CH2
CH2 → CH3CH
CHCH3
C)∙ RO∙ + CH2
CH2 → ROCH2
CH2
D)∙ ∙ ROCH2CH2 + CH2
CH2 → ROCH2CH2CH2CH2
E)∙ 2 RO-[CH2CH2]n-CH2CH2 →
RO-[CH2CH2]n-CH2CH2CH2CH2-[CH2CH2]n-OR
A)ROOR + CH2
![<strong>Which of the following is a possible step to terminate a chain in the radical polymerization of ethylene?</strong> A)ROOR + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub>CH<sub>2</sub>OR B)CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → CH<sub>3</sub>CH CHCH<sub>3</sub> C)∙ RO∙ + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub> <sub> </sub> CH<sub>2</sub> D)∙ ∙ ROCH<sub>2</sub>CH<sub>2</sub> + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub> E)∙ 2 RO-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-CH<sub>2</sub>CH<sub>2</sub> → RO-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-OR](https://storage.examlex.com/TB1831/11ea8a1c_2db4_9cb4_b657_25208dcdd4f7_TB1831_11.jpg)
B)CH2
![<strong>Which of the following is a possible step to terminate a chain in the radical polymerization of ethylene?</strong> A)ROOR + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub>CH<sub>2</sub>OR B)CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → CH<sub>3</sub>CH CHCH<sub>3</sub> C)∙ RO∙ + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub> <sub> </sub> CH<sub>2</sub> D)∙ ∙ ROCH<sub>2</sub>CH<sub>2</sub> + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub> E)∙ 2 RO-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-CH<sub>2</sub>CH<sub>2</sub> → RO-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-OR](https://storage.examlex.com/TB1831/11ea8a1c_2db4_c3c5_b657_69865b571643_TB1831_11.jpg)
![<strong>Which of the following is a possible step to terminate a chain in the radical polymerization of ethylene?</strong> A)ROOR + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub>CH<sub>2</sub>OR B)CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → CH<sub>3</sub>CH CHCH<sub>3</sub> C)∙ RO∙ + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub> <sub> </sub> CH<sub>2</sub> D)∙ ∙ ROCH<sub>2</sub>CH<sub>2</sub> + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub> E)∙ 2 RO-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-CH<sub>2</sub>CH<sub>2</sub> → RO-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-OR](https://storage.examlex.com/TB1831/11ea8a1c_2db4_c3c6_b657_d306cf432b03_TB1831_11.jpg)
![<strong>Which of the following is a possible step to terminate a chain in the radical polymerization of ethylene?</strong> A)ROOR + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub>CH<sub>2</sub>OR B)CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → CH<sub>3</sub>CH CHCH<sub>3</sub> C)∙ RO∙ + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub> <sub> </sub> CH<sub>2</sub> D)∙ ∙ ROCH<sub>2</sub>CH<sub>2</sub> + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub> E)∙ 2 RO-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-CH<sub>2</sub>CH<sub>2</sub> → RO-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-OR](https://storage.examlex.com/TB1831/11ea8a1c_2db4_c3c7_b657_23654ca9dcbb_TB1831_11.jpg)
C)∙ RO∙ + CH2
![<strong>Which of the following is a possible step to terminate a chain in the radical polymerization of ethylene?</strong> A)ROOR + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub>CH<sub>2</sub>OR B)CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → CH<sub>3</sub>CH CHCH<sub>3</sub> C)∙ RO∙ + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub> <sub> </sub> CH<sub>2</sub> D)∙ ∙ ROCH<sub>2</sub>CH<sub>2</sub> + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub> E)∙ 2 RO-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-CH<sub>2</sub>CH<sub>2</sub> → RO-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-OR](https://storage.examlex.com/TB1831/11ea8a1c_2db4_ead8_b657_bb3bffe7df39_TB1831_11.jpg)
![<strong>Which of the following is a possible step to terminate a chain in the radical polymerization of ethylene?</strong> A)ROOR + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub>CH<sub>2</sub>OR B)CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → CH<sub>3</sub>CH CHCH<sub>3</sub> C)∙ RO∙ + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub> <sub> </sub> CH<sub>2</sub> D)∙ ∙ ROCH<sub>2</sub>CH<sub>2</sub> + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub> E)∙ 2 RO-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-CH<sub>2</sub>CH<sub>2</sub> → RO-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-OR](https://storage.examlex.com/TB1831/11ea8a1c_2db4_ead9_b657_57b192fbefa0_TB1831_11.jpg)
D)∙ ∙ ROCH2CH2 + CH2
![<strong>Which of the following is a possible step to terminate a chain in the radical polymerization of ethylene?</strong> A)ROOR + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub>CH<sub>2</sub>OR B)CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → CH<sub>3</sub>CH CHCH<sub>3</sub> C)∙ RO∙ + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub> <sub> </sub> CH<sub>2</sub> D)∙ ∙ ROCH<sub>2</sub>CH<sub>2</sub> + CH<sub>2</sub> <sub> </sub> CH<sub>2</sub> → ROCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub> E)∙ 2 RO-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-CH<sub>2</sub>CH<sub>2</sub> → RO-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>-[CH<sub>2</sub>CH<sub>2</sub>]<sub>n</sub>-OR](https://storage.examlex.com/TB1831/11ea8a1c_2db5_11ea_b657_8f194feaf955_TB1831_11.jpg)
E)∙ 2 RO-[CH2CH2]n-CH2CH2 →
RO-[CH2CH2]n-CH2CH2CH2CH2-[CH2CH2]n-OR
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7
Chain-growth polymerization proceeds by which of the following mechanisms?
A)radical polymerization
B)cationic polymerization
C)anionic polymerization
D)A and B
E)A,B,and C
A)radical polymerization
B)cationic polymerization
C)anionic polymerization
D)A and B
E)A,B,and C
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8
Which of the following species can best serve as an initiator for anionic polymerization?
A)CH3CH2CH2CH2Li
B)BF3
C)HOOH
D)CH3CH2CH2CH2OH
E)CH3CH2CH2CH2OCH2CH2CH2CH3
A)CH3CH2CH2CH2Li
B)BF3
C)HOOH
D)CH3CH2CH2CH2OH
E)CH3CH2CH2CH2OCH2CH2CH2CH3
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9
Which of the following statements best describes what alpha olefins are?
A)polysubstituted ethylenes
B)monosubstituted ethylenes
C)disubstituted ethylenes
D)ethylenes
E)isoprenes
A)polysubstituted ethylenes
B)monosubstituted ethylenes
C)disubstituted ethylenes
D)ethylenes
E)isoprenes
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10
Which of the following species can best serve as an initiator for cationic polymerization?
A)ROOR
B)ROH
C)ROR
D)AlCl3
E)RCOOR
A)ROOR
B)ROH
C)ROR
D)AlCl3
E)RCOOR
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11
The choice of mechanism in chain-growth polymerization depends on which of the following?
A)structure of the monomer and initiator used
B)structure of the polymer and initiator used
C)temperature and pressure of the reaction
D)A and B
E)A,B,and C
A)structure of the monomer and initiator used
B)structure of the polymer and initiator used
C)temperature and pressure of the reaction
D)A and B
E)A,B,and C
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12
What is the structure of the monomer from which the following polymer is made? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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13
What is the structure of the monomer from which the following polymer is made? 
A)CH3CH3
B)CH2
CH2
C)CH3CH
CH2
D)CH2
CHCH
CH2
E)CH3CH
CHCH3

A)CH3CH3
B)CH2

C)CH3CH

D)CH2


E)CH3CH

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14
Draw the structure of the polymer and by-product that result when the two monomers below are heated together. 

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15
Which of the following is more likely to undergo both radical and cationic polymerization? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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16
Which of the following are characteristic of linear polyethylene?
A)They are branched polymers.
B)They are known as high-density polyethylene.
C)They are soft and flexible polymers.
D)A and B
E)A and C
A)They are branched polymers.
B)They are known as high-density polyethylene.
C)They are soft and flexible polymers.
D)A and B
E)A and C
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17
Chain-growth polymerization exhibits a marked preference for
A)tail-to-tail addition
B)head-to-head addition
C)head-to-tail addition
D)head-to-middle addition
E)middle-to-tail addition
A)tail-to-tail addition
B)head-to-head addition
C)head-to-tail addition
D)head-to-middle addition
E)middle-to-tail addition
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18
Which of the following monomers has the greatest ability to undergo anionic polymerization? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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19
Which of the following species can best serve as a radical initiator for radical polymerization?
A)ROH
B)ROR
C)ROOR
D)RCOOR
E)RCOOH
A)ROH
B)ROR
C)ROOR
D)RCOOR
E)RCOOH
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20
Which of the following statements best explains the process known as chain transfer?
A)a process that can control the rate of production of the polymer
B)a process that can control the molecular weight of the polymer
C)a process that can control the reactivity of the monomer
D)a process that can slow down the polymerization reaction
E)a process that can inhibit the polymerization reaction
A)a process that can control the rate of production of the polymer
B)a process that can control the molecular weight of the polymer
C)a process that can control the reactivity of the monomer
D)a process that can slow down the polymerization reaction
E)a process that can inhibit the polymerization reaction
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21
From which of the following compounds is Lucite or poly(methyl methacrylate)prepared?
A)CH2
CHCH3
B)CH2
C(CH3)O2CCH3
C)CH2
CHO2CCH3
D)CH2
C(CH3)CO2CH3
E)CH2
CHCO2CH3
A)CH2

B)CH2

C)CH2

D)CH2

E)CH2

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22
List the three phases in the mechanism of chain-growth polymerization.
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23
Which is not typically made through radical polymerization?
A)poly(styrene)
B)PVC
C)Dacron
D)poly(vinyl acetate)
E)Lucite
A)poly(styrene)
B)PVC
C)Dacron
D)poly(vinyl acetate)
E)Lucite
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24
In a recycling symbol,the ________ the number in the middle of the symbol,the more easily the compound can be recycled.
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25
Propose a synthesis of poly(vinyl alcohol)from H2C
CHO2CCH3.

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26
Which of the following is more likely to form non-terminated polymeric chains called living polymers?
A)cationic polymerization
B)free radical polymerization
C)anionic polymerization
D)A and B
E)A and C
A)cationic polymerization
B)free radical polymerization
C)anionic polymerization
D)A and B
E)A and C
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27
When 2,2-dimethyloxirane (see figure below)undergoes anionic polymerization,the nucleophile attacks the least substituted carbon of the epoxide,but when it undergoes cationic polymerization,the nucleophile attacks the most substituted carbon of the epoxide.Explain why this is so. 

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28
When 3-methyl-1-butene
CH2
CHCH(CH3)2
undergoes cationic polymerization,the following expected carbocation is formed.
⊕
X-CH2-CH-CH(CH3)2
However,the following carbocation is also found in the reaction.
⊕
X-CH2-CH2-C(CH3)2
Explain.
CH2

undergoes cationic polymerization,the following expected carbocation is formed.
⊕
X-CH2-CH-CH(CH3)2
However,the following carbocation is also found in the reaction.
⊕
X-CH2-CH2-C(CH3)2
Explain.
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29
What structural characteristic is shared by compounds used as radical initiators?
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30
Show how branching could occur during the free-radical polymerization of styrene.
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31
What are common factors that enter into the choice of radical initiators for chain-growth polymerization?
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32
Provide a mechanism to show how H2C
CHCO2CH3 is polymerized using butyllithium as the initiator.

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33
Which of the following monomers is least likely to undergo cationic polymerization?
A)propylene
B)isobutylene
C)styrene
D)methyl acrylate
E)vinyl acetate
A)propylene
B)isobutylene
C)styrene
D)methyl acrylate
E)vinyl acetate
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34
Explain why some monomers are better able to undergo chain-growth polymerization by a radical mechanism.
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35
Provide a mechanism to show how H2C
C(CH3)2 is polymerized using BF3 as the initiator.

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36
Show the mechanism for the formation of a segment of polystyrene containing two molecules of styrene and initiated by hydrogen peroxide.
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37
Which of the following can result in chain termination in cationic polymerization?
A)loss of H+
B)addition of a nucleophile that reacts with the propagating site
C)a chain transfer reaction with the solvent
D)a 1,2-hydride shift.
E)A,B,and C
A)loss of H+
B)addition of a nucleophile that reacts with the propagating site
C)a chain transfer reaction with the solvent
D)a 1,2-hydride shift.
E)A,B,and C
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38
Show the three methods by which the following radical can be terminated. 

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39
Show the reaction which occurs when benzoyl peroxide is heated.
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40
Provide the structure of the monomer from which Orlon [poly(acrylonitrile)] is prepared.
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41
Draw the monomer for poly(vinyl acetate).
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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42
Provide the structure of poly(propylene).
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43
What is the main structural difference between high-density and low-density polyethylene,and how does this structural difference affect the properties and uses of these polymers?
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44
Draw the structure of the polymer that results when methyl α-cyanoacrylate undergoes polymerization.By what name is this polymer commonly known?
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45
Identify the monomer(s)that undergo anionic polymerization.You may choose more than one answer.
A)styrene
B)methyl methacrylate
C)vinyl chloride
D)methyl vinyl ether
E)acrylamide
A)styrene
B)methyl methacrylate
C)vinyl chloride
D)methyl vinyl ether
E)acrylamide
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46
Provide the structure of poly(vinyl chloride).
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47
Give the monomer for the polymer teflon.
A)propylene
B)acrylonitrile
C)tetrafluoroethylene
D)poly(vinyl acetate)
E)styrene
A)propylene
B)acrylonitrile
C)tetrafluoroethylene
D)poly(vinyl acetate)
E)styrene
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48
Identify the initiator in a radical polymerization.
A)KOH
B)BuLi
C)CH3OOCH3
D)BF3,H2O
E)HCl
A)KOH
B)BuLi
C)CH3OOCH3
D)BF3,H2O
E)HCl
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49
Identify the monomer for superglue.
A)acrylamide
B)methyl a-cyanoacrylate
C)acrolein
D)methyl vinyl ether
E)styrene
A)acrylamide
B)methyl a-cyanoacrylate
C)acrolein
D)methyl vinyl ether
E)styrene
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50
Draw a short segment of neoprene,using four monomers.
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51
Is acrylonitrile more likely to undergo anionic or cationic polymerization? Explain your answer.
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52
Identify the monomer(s)that undergo cationic polymerization.You may choose more than one answer.
A)styrene
B)methyl methacrylate
C)vinyl chloride
D)methyl vinyl ether
E)acrylamide
A)styrene
B)methyl methacrylate
C)vinyl chloride
D)methyl vinyl ether
E)acrylamide
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53
What advantage does a Lewis acid like BF3 have over a proton-donating acid like HCl as a initiator in cationic polymerization?
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54
Why is chain branching less common in anionic polymerization than in cationic polymerization?
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55
Provide the structure of poly(acrylonitrile).
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56
Draw a short segment of plexiglass,using five monomers.
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57
Identify the initiator in a cationic polymerization.
A)KOH
B)BuLi
C)CH3OOCH3
D)BF3,H2O
E)HCl
A)KOH
B)BuLi
C)CH3OOCH3
D)BF3,H2O
E)HCl
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58
Identify the initiator in an anionic polymerization.
A)KOH
B)BuLi
C)CH3OOCH3
D)BF3,H2O
E)HCl
A)KOH
B)BuLi
C)CH3OOCH3
D)BF3,H2O
E)HCl
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59
What is the mass of each repeating unit in poly(ethylene)?
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60
Identify the monomer(s)that undergo radical polymerization.You may choose more than one answer.
A)styrene
B)methyl methacrylate
C)vinyl chloride
D)methyl vinyl ether
E)acrylamide
A)styrene
B)methyl methacrylate
C)vinyl chloride
D)methyl vinyl ether
E)acrylamide
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61
The pattern below is found in what type of polymer? AABBBABAABABBAAB
A)an alternating copolymer
B)a block copolymer
C)a random copolymer
D)a graft copolymer
E)a homopolymer
A)an alternating copolymer
B)a block copolymer
C)a random copolymer
D)a graft copolymer
E)a homopolymer
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62
Draw the structure of the polymer produced in the following reaction. 

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63
ABS is a copolymer of what three monomers?
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64
Identify the type of polymer for nylon 66.
A)homopolymer
B)graft copolymer
C)random copolymer
D)block copolymer
E)alternating copolymer
A)homopolymer
B)graft copolymer
C)random copolymer
D)block copolymer
E)alternating copolymer
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65
The pattern below is found in what type of polymer? AAAABBBBAAAABBBB
A)an alternating copolymer
B)a block copolymer
C)a random copolymer
D)a graft copolymer
E)a homopolymer
A)an alternating copolymer
B)a block copolymer
C)a random copolymer
D)a graft copolymer
E)a homopolymer
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66
Provide the structure of Saran,an alternating copolymer of H2C
CHCl and H2C
CCl2.


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67
Which of the following polymers is arranged in an isotactic configuration? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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68
Natural rubber is a
A)polyamide.
B)polyester.
C)polycarbonate.
D)polyurethane.
E)none of the above.
A)polyamide.
B)polyester.
C)polycarbonate.
D)polyurethane.
E)none of the above.
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69
From which of the following monomers is neoprene synthesized?
A)(Z)-2-chloro-2-butene
B)(E)-2-chloro-2-butene
C)(E)-1-chloro-1,3-butadiene
D)2-chloro-1,3-butadiene
E)2,3-dichloro-1,3-butadiene
A)(Z)-2-chloro-2-butene
B)(E)-2-chloro-2-butene
C)(E)-1-chloro-1,3-butadiene
D)2-chloro-1,3-butadiene
E)2,3-dichloro-1,3-butadiene
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70
What are aramides?
A)aromatic polyester polymers
B)aromatic amine polymers
C)alkyl halide polymers
D)aromatic polyamide polymers
E)aliphatic polyamide polymers
A)aromatic polyester polymers
B)aromatic amine polymers
C)alkyl halide polymers
D)aromatic polyamide polymers
E)aliphatic polyamide polymers
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71
Identify the type of polymer for poly(vinyl chloride).
A)homopolymer
B)graft copolymer
C)random copolymer
D)block copolymer
E)alternating copolymer
A)homopolymer
B)graft copolymer
C)random copolymer
D)block copolymer
E)alternating copolymer
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72
What is the difference between natural rubber and Gutta-percha rubber?
A)Natural rubber is hard and brittle while gutta-percha is soft and rubbery.
B)Natural rubber is natural while gutta-percha is synthetic rubber.
C)Natural rubber has a cis configuration while gutta-percha has a trans configuration.
D)Natural rubber and gutta-percha rubber are enantiomers.
E)The monomer for natural rubber is isoprene while the monomer for gutta-percha is 1,3-butadiene.
A)Natural rubber is hard and brittle while gutta-percha is soft and rubbery.
B)Natural rubber is natural while gutta-percha is synthetic rubber.
C)Natural rubber has a cis configuration while gutta-percha has a trans configuration.
D)Natural rubber and gutta-percha rubber are enantiomers.
E)The monomer for natural rubber is isoprene while the monomer for gutta-percha is 1,3-butadiene.
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73
Kevlar is an example of
A)a polyester.
B)an aramide.
C)a polyurethane.
D)a epoxy resin.
E)a plasticizer.
A)a polyester.
B)an aramide.
C)a polyurethane.
D)a epoxy resin.
E)a plasticizer.
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74
Which of the following statements best describes what vulcanization means?
A)a process by which rigid and non-sticky rubber can be made soft and sticky
B)a chemical process discovered by Charles Schultz in 1944
C)the heating of rubber with sulfur
D)a chemical process that destroys cross-linking in rubber
E)all of the above
A)a process by which rigid and non-sticky rubber can be made soft and sticky
B)a chemical process discovered by Charles Schultz in 1944
C)the heating of rubber with sulfur
D)a chemical process that destroys cross-linking in rubber
E)all of the above
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75
Provide the structure of poly(tetrafluoroethylene).
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76
Which of the following statements concerning the stereochemistry of polymerization is correct?
A)Polymers in the atactic configuration are more likely to be crystalline solids because regular packing of the polymer chains is easier.
B)Polymers in the isotactic configuration tend to be softer and more flexible than atactic polymers.
C)In general,radical polymerization leads primarily to branched polymers in the syndiotactic configuration.
D)The percentage of chains in the isotactic or syndiotactic configuration decreases as the polymerization temperature decreases.
E)none of the above
A)Polymers in the atactic configuration are more likely to be crystalline solids because regular packing of the polymer chains is easier.
B)Polymers in the isotactic configuration tend to be softer and more flexible than atactic polymers.
C)In general,radical polymerization leads primarily to branched polymers in the syndiotactic configuration.
D)The percentage of chains in the isotactic or syndiotactic configuration decreases as the polymerization temperature decreases.
E)none of the above
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77
Which of the following is a step-growth polymer?
A)polyethylene
B)polyester
C)polypropylene
D)polystyrene
E)Plexiglass
A)polyethylene
B)polyester
C)polypropylene
D)polystyrene
E)Plexiglass
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78
A substituted ethylene polymer in which the substituents are randomly oriented is called
A)a ditactic polymer.
B)an eutatic polymer.
C)an isotactic polymer.
D)a syndiotatic polymer.
E)an atactic polymer.
A)a ditactic polymer.
B)an eutatic polymer.
C)an isotactic polymer.
D)a syndiotatic polymer.
E)an atactic polymer.
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79
Name the monomer used in the production of neoprene.
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80
Which of the following initiators are known as Ziegler-Natta catalysts,which were discovered in 1953 in order to control the stereochemistry of polymers?
A)Al/Ti initiators
B)Ni/Cd initiators
C)Zn/Hg initiators
D)Pb/C initiators
E)Pb/PbO2 initiators
A)Al/Ti initiators
B)Ni/Cd initiators
C)Zn/Hg initiators
D)Pb/C initiators
E)Pb/PbO2 initiators
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