Deck 16: Organic Polymer Chemistry
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Deck 16: Organic Polymer Chemistry
1
Which polymers will be strongest?
A) PET 0% crystallinity
B) PET 20% crystallinity
C) PET 35% crystallinity
D) PET 55% crystallinity
A) PET 0% crystallinity
B) PET 20% crystallinity
C) PET 35% crystallinity
D) PET 55% crystallinity
PET 55% crystallinity
2
Which polymers will be brittle at 0° C?
I. PVC, Tg = 83° C
II. PVA, Tg = 200° C
III. teflon, Tg = -80° C
IV. polypropylene, Tg = -100° C
A) III, IV
B) II, III
C) I, II
D) II, IV
I. PVC, Tg = 83° C
II. PVA, Tg = 200° C
III. teflon, Tg = -80° C
IV. polypropylene, Tg = -100° C
A) III, IV
B) II, III
C) I, II
D) II, IV
I, II
3
What is characteristic of the process of Step-Growth Polymerization?
I. In the beginning of the polymerization process, there are many oligomers (an oligomer is made from a few monomers, its chain length is short).
II. High macromolecular weights are only reached at the very end of the polymerization process.
III. If two bifunctional monomers (e.g. diamine and dicarboxylic acid) are used, slight deviations from 1:1 stoichiometry will prevent high macromolecular weights at the end of the polymerization process.
IV. Polymer chains can grow individually to high macromolecular weight at any time during the polymerization process.
A) I and II
B) II and III
C) I, II and III
D) II and IV
I. In the beginning of the polymerization process, there are many oligomers (an oligomer is made from a few monomers, its chain length is short).
II. High macromolecular weights are only reached at the very end of the polymerization process.
III. If two bifunctional monomers (e.g. diamine and dicarboxylic acid) are used, slight deviations from 1:1 stoichiometry will prevent high macromolecular weights at the end of the polymerization process.
IV. Polymer chains can grow individually to high macromolecular weight at any time during the polymerization process.
A) I and II
B) II and III
C) I, II and III
D) II and IV
I, II and III
4
Which polymers are correctly classified? 
A) I, III
B) II, III
C) III, IV
D) II, IV

A) I, III
B) II, III
C) III, IV
D) II, IV
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5
Which characteristics are found in polymers with low degrees of crystallinity?
I. large molecular side groups
II. high Tm
III. strong intermolecular forces
IV. elasticity
A) I, III
B) II, III
C) III, IV
D) I, IV
I. large molecular side groups
II. high Tm
III. strong intermolecular forces
IV. elasticity
A) I, III
B) II, III
C) III, IV
D) I, IV
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6
What small molecules can be released during Step-Growth-Polymerization?
I. H2O
II. NH3
III. methanol
IV. none
A) I
B) II, III
C) I, III
D) IV
I. H2O
II. NH3
III. methanol
IV. none
A) I
B) II, III
C) I, III
D) IV
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7
Which of the following are typical polymer architectures?
I. linear
II. tetrahedral
III. star
IV. ladder
V. forked
A) II, III, IV
B) III, IV, V
C) I, III, IV
D) I, II, IV
I. linear
II. tetrahedral
III. star
IV. ladder
V. forked
A) II, III, IV
B) III, IV, V
C) I, III, IV
D) I, II, IV
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8
Which characteristics are found in polymers with high degrees of crystallinity?
I. regular, compact structures
II. high Tm
III. weak intermolecular forces
IV. elasticity
A) I, III
B) I, II
C) III, IV
D) II, IV
I. regular, compact structures
II. high Tm
III. weak intermolecular forces
IV. elasticity
A) I, III
B) I, II
C) III, IV
D) II, IV
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9
Which pair of compounds would react to form the polymer shown?

A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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10
Which polymers are step-growth polymers?
I. Polyamides (e.g.Kevlar)
II. Polyesters (e.g.Mylar)
III. PVC
IV. PMMA (e.g. Lucite)
A) I, II
B) II, III
C) I, IV
D) III, IV
I. Polyamides (e.g.Kevlar)
II. Polyesters (e.g.Mylar)
III. PVC
IV. PMMA (e.g. Lucite)
A) I, II
B) II, III
C) I, IV
D) III, IV
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11
Which terms are matched correctly with their definitions?
I. Crystalline domain - order regions in the solid state of a polymer.
II. Amorphous domain - disordered regions in the solid state of a polymer.
III. Melt transition temperature - temperature at which a polymer undergoes the transition from
Hard to rubbery state.
IV. Glass transition temperature - temperature at which glass polymers melt.
A) II, III
B) III, IV
C) I, IV
D) I, II
I. Crystalline domain - order regions in the solid state of a polymer.
II. Amorphous domain - disordered regions in the solid state of a polymer.
III. Melt transition temperature - temperature at which a polymer undergoes the transition from
Hard to rubbery state.
IV. Glass transition temperature - temperature at which glass polymers melt.
A) II, III
B) III, IV
C) I, IV
D) I, II
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12
Which pair of compounds would react to form the polymer shown?

A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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13
Which classification best describes the mechanism of the synthesis of polyamides via step growth polymerization?
A) nucleophilic acyl addition
B) nucleophilic acyl substitution
C) electrophilic addition
D) radical substitution
A) nucleophilic acyl addition
B) nucleophilic acyl substitution
C) electrophilic addition
D) radical substitution
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14
Which pair of compounds would react to form the polymer shown under appropriate reaction conditions?

A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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15
Which polymers are correctly classified? 
A) II, III
B) III, IV
C) I, IV
D) I, II

A) II, III
B) III, IV
C) I, IV
D) I, II
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16
Which terms are correctly matched to their definitions?
I. Plastic - a long chain molecule synthesized by linking together many single parts.
II. Polymer - can be molded when hot and retains its shape when cooled.
III. Thermoplastic - can be molded when hot and retains its shape when cooled.
IV. Thermosetting plastic - can be molded when first prepared, but hardens irreversibly when
Cooled.
A) III, IV
B) II, III
C) I, II
D) I, IV
I. Plastic - a long chain molecule synthesized by linking together many single parts.
II. Polymer - can be molded when hot and retains its shape when cooled.
III. Thermoplastic - can be molded when hot and retains its shape when cooled.
IV. Thermosetting plastic - can be molded when first prepared, but hardens irreversibly when
Cooled.
A) III, IV
B) II, III
C) I, II
D) I, IV
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17
Why can any nylon-polymer not be used as an insulator in lead/sulfuric acid batteries?
A) PbO2 would oxidize the polymer.
B) Aqueous H2SO4 would hydrolyze the amide-bonds.
C) Aqueous H2SO4 would dissolve the polymer.
D) Pb would reduce nylon to a polyamine.
A) PbO2 would oxidize the polymer.
B) Aqueous H2SO4 would hydrolyze the amide-bonds.
C) Aqueous H2SO4 would dissolve the polymer.
D) Pb would reduce nylon to a polyamine.
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18
Which polymers will be the most elastic?
A) PET 0% crystallinity
B) PET 20% crystallinity
C) PET 35% crystallinity
D) PET 55% crystallinity
A) PET 0% crystallinity
B) PET 20% crystallinity
C) PET 35% crystallinity
D) PET 55% crystallinity
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19
Which polymers will be elastic at 0° C?
I. PVC, Tg = 83° C
II. PVA, Tg = 200° C
III. teflon, Tg = -80° C
IV. polypropylene, Tg = -100° C
A) III, IV
B) II, III
C) I, II
D) II, IV
I. PVC, Tg = 83° C
II. PVA, Tg = 200° C
III. teflon, Tg = -80° C
IV. polypropylene, Tg = -100° C
A) III, IV
B) II, III
C) I, II
D) II, IV
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20
Which polymers are step-growth polymers?
I. nylon
II. HDPE
III. Teflon
IV. PET
A) I, II
B) II, III
C) I, IV
D) III, IV
I. nylon
II. HDPE
III. Teflon
IV. PET
A) I, II
B) II, III
C) I, IV
D) III, IV
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21
Which polymers are correctly matched to their primary use?
I. Kevlar and containers
II. Polymethylmethacrylate and Plexiglas
III. Polytetrafluoroethylene and nonstick coatings
IV. PET and bulletproof vests
A) I, III
B) II, III
C) II, IV
D) III, IV
I. Kevlar and containers
II. Polymethylmethacrylate and Plexiglas
III. Polytetrafluoroethylene and nonstick coatings
IV. PET and bulletproof vests
A) I, III
B) II, III
C) II, IV
D) III, IV
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22
Before recycling, plastics are sorted according to their resin identification code, which was developed by the Society of the Plastics Industry in 1988. Presorting is necessary, because of the following physical and chemical characteristics of polymers:
I. Polymers have a tendency to phase-separate when molten.
II. Different polymers have very different decomposition temperatures.
III. Polymers featuring very high melting temperatures decompose into smaller molecules at high temperatures rather than melt.
IV. Molten polymers mix easily.
A) I, II, IV
B) II, III
C) I, II, III
D) all of the above
I. Polymers have a tendency to phase-separate when molten.
II. Different polymers have very different decomposition temperatures.
III. Polymers featuring very high melting temperatures decompose into smaller molecules at high temperatures rather than melt.
IV. Molten polymers mix easily.
A) I, II, IV
B) II, III
C) I, II, III
D) all of the above
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23
Keratins are a family of tough and insoluble proteins that are able to form fibers. They form the hard but unmineralized (not bony) structures in amphibians, mammals and reptiles/birds. Keratin, a byproduct from the poultry industry, has recently sparked interest. Keratins are made from a high proportion of the amino acid glycine (R=H), followed by the amino acid alanine (R=-CH3). Two neighboring strands of keratin are shown below.
To what class of polymers is Keratin quite similar?
A) polyesters, such as PET
B) polyamides, such as nylon
C) polyalkenes, such as polyacrylate
D) polyurethanes
To what class of polymers is Keratin quite similar?

A) polyesters, such as PET
B) polyamides, such as nylon
C) polyalkenes, such as polyacrylate
D) polyurethanes
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24
The polymer (PEN) synthesized from the following monomers
is
is

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25
A carbonate, which forms the backbone of polycarbonates, has the following structure, 

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26
What small molecules can be released during Chain-Growth-Polymerization?
A) H2O
B) NH3
C) methanol
D) none
A) H2O
B) NH3
C) methanol
D) none
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27
Determine the repeat unit for the following polymer.

A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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28
What is characteristic of the process of Chain-Growth Polymerization
I. In the beginning of the polymerization process, there are many oligomers (an oligomer is made from a few monomers, its chain length is short).
II. High macromolecular weights are only reached at the very end of the polymerization process.
III. The macromolecular weight of the polymer chains grows approximately linear during the time required for the polymerization process.
IV. Polymer chains grow by addition of monomers to the polymer.
A) I, II
B) II, III
C) III, IV
D) II, IV
I. In the beginning of the polymerization process, there are many oligomers (an oligomer is made from a few monomers, its chain length is short).
II. High macromolecular weights are only reached at the very end of the polymerization process.
III. The macromolecular weight of the polymer chains grows approximately linear during the time required for the polymerization process.
IV. Polymer chains grow by addition of monomers to the polymer.
A) I, II
B) II, III
C) III, IV
D) II, IV
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29
The structure of the polymer (Nylon 6,12), synthesized from the following monomers,
is
is

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30
Which polymers are chain-growth polymers?
I. Polyamides (e.g. Kevlar)
II. Polyesters (e.g.Mylar)
III. PVC
IV. PMMA(e.g. Lucite)
A) I, II
B) II, III
C) I, IV
D) III, IV
I. Polyamides (e.g. Kevlar)
II. Polyesters (e.g.Mylar)
III. PVC
IV. PMMA(e.g. Lucite)
A) I, II
B) II, III
C) I, IV
D) III, IV
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31
A diepoxide, which forms the backbone of epoxy resins, has the following structure, 

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32
Which polymers are chain-growth polymers?
I. nylon
II. HDPE
III. Teflon
IV. PET
A) I, II
B) II, III
C) I, IV
D) III, IV
I. nylon
II. HDPE
III. Teflon
IV. PET
A) I, II
B) II, III
C) I, IV
D) III, IV
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33
Principally, the anhydrous depolymerization of Chain-Growth polymers into their monomers would/will have the following advantages, compared to hydrous pyrolysis of plastics?
I. The yield of alkene-monomers, that can be repolymerized, would be higher.
II. If several monomers are formed, they can be separated by distillation.
III. The use of polymerization/depolymerization catalysts permits lower process temperatures than during the hydrous pyrolysis, in which the heat is supplied by superheated water.
IV. A greater variety of small organic compounds will be formed.
A) I, II
B) I, II, III
C) II, III, IV
D) I, III, IV
I. The yield of alkene-monomers, that can be repolymerized, would be higher.
II. If several monomers are formed, they can be separated by distillation.
III. The use of polymerization/depolymerization catalysts permits lower process temperatures than during the hydrous pyrolysis, in which the heat is supplied by superheated water.
IV. A greater variety of small organic compounds will be formed.
A) I, II
B) I, II, III
C) II, III, IV
D) I, III, IV
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34
Kapton is a polyimide developed by DuPont which has an excellent stability in the temperature range of 0K to 673K). Therefore, it is widely used in the aircraft and space industry although its resistance to mechanical wear is inferior to that of other polymers, such as Mylar (polyethylene terephthalate). Which of the following molecules can be either starting materials or intermediates in the synthesis of Kapton? 
A) I, II
B) II, III
C) I, III
D) III, IV

A) I, II
B) II, III
C) I, III
D) III, IV
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35
Which is not a step in the mechanism of a chain growth polymerization?
A) initiation
B) propagation
C) proliferation
D) termination
A) initiation
B) propagation
C) proliferation
D) termination
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36
Which statements are true describing the Ziegler-Natta process?
I. the process yields low density polyethylene
II. the process involves radicals
III. the original process used an alkytitanium catalyst
IV. the process yields polyethylene 3 to 10 times stronger than other methods
A) I, II
B) II, IV
C) II, III
D) III, IV
I. the process yields low density polyethylene
II. the process involves radicals
III. the original process used an alkytitanium catalyst
IV. the process yields polyethylene 3 to 10 times stronger than other methods
A) I, II
B) II, IV
C) II, III
D) III, IV
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37
Determine the repeat unit for the following polymer.

A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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38
The monomers used to synthesize Nomex are


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39
How can one distinguish between polyethylene-terephthalate and polystyrene during the process of recycling?
I. the IR-spectra are different
II. different glass temperatures
III. different crystallinity
IV. different polymer density
A) I, II
B) II, III
C) III, IV
D) I, IV
I. the IR-spectra are different
II. different glass temperatures
III. different crystallinity
IV. different polymer density
A) I, II
B) II, III
C) III, IV
D) I, IV
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40
Which compound would react to form the polymer shown?

A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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41
The opacity of a crystalline polymer correlates to the Tm.
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42
The repeat unit of polyacrylonitrile is


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43
The label of the following step of radical chain polymerization is __________________________. 

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44
An elastomer with a glass transition temperature (Tg) of 25° C will lose its elasticity below 25° C.
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45
The monomers used to synthesize the following polyurethane are,


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46
Branching of polyethylene, due to a chain transfer reaction, produces low-density polyethylene (LDPE).
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47
Poly-3- hydroxybutanoic acid is a biodegradable polymer. Complete the reaction scheme shown below, which leads to the synthesis of poly-3-hydroxybutanoic acid. 

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48
Complete the mechanism of the ring-opening and subsequent polymerization of caprolactam. This reaction proceeds at higher temperatures (> 150oC). 

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49
A polymer synthesized from the following monomers could have the form


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50
A polymer with a melt transition temperature (Tm) of 200° C is stronger than a polymer with a Tm of 150° C.
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51
A polymer synthesized from the following monomers could have the form


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52
The glass transition temperature (Tg) must be low for an elastomer to maintain its properties.
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53
The Zeigler-Natta process yields low-density polyethylene (LDPE).
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54
Radical chain growth polymers tend to form head to head bonds between carbon one of one monomer and carbon one of another monomer.
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55
The polymer synthesized from the following monomer is 

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56
The repeat unit of polymethylacrylate is,


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57
Complete the mechanism for radical chain propagation begun below. 

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58
Poly-amino-levulinic acid is a biodegradable polymer. Complete the reaction scheme shown below, which leads to the synthesis of poly-amino-levulinic acid: 

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