(a)
Interpretation: The structure of prepolymer A formed from
Concept introduction:
(b)
Interpretation: The structure of
Concept introduction: Epoxides are strained three-membered rings. They undergo anionic polymerization to afford the ring opening, by following the
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- (a) Hard contact lenses, which first became popular in the 1960s, were made by polymerizing methyl methacrylate [CH2=C(CH3)CO2CH3] to form poly(methyl methacrylate) (PMMA). Draw the structure of PMMA. (b) More-comfortable softer contact lenses introduced in the 1970s were made by polymerizing hydroxyethyl methacrylate [CH2=C(CH3)CO2CH2CH2OH] to form poly(hydroxyethyl methacrylate) (poly-HEMA). Draw the structure of poly-HEMA. Because neither polymer allows oxygen from the air to pass through to the retina, newer contact lenses that are both comfortable and oxygen-permeable have now been developed.arrow_forward(a) Draw the structure of polystyrene, which is formed by polymerizing the monomer styrene, C6H5CH=CH2.arrow_forward3. Dacron is the brand name for the polymer that is made from ethane-1,2-diol and benzene-1,4-dicarboxylic acid. (a) What type of polymer is Dacron? (b) When the two monomers combine, what type of reaction do they undergo and what molecule is eliminated? (c) What is the name for the linkages that join the monomers together?(d) Draw the monomers and the polymer of the reaction to create Dacron. (Use a condensed structural formula in your answer.) HC-C styrene H-O-C- ethane-1,2-diol I H OH НО. 206 H -C-0-H H benzene-1.4-dicarboxylic acid.arrow_forward
- A polymer closely related to PET is PBT, which is made from terephthalic acid and butane-1,4-diol.(a) Propose a structure for PBT and write the condensed formula for the structure.(b) What does PBT stand for? That is, what do you expect the trivial name of PBT to be?(c) Would you expect PBT to have a higher or lower melting point than PET? Justify your answer.(d) PBT, rather than PET, is used in molding because it crystallizes faster. Explain why PBT crystallizes more quickly than PET.arrow_forward(b) Draw the structures of the polymers obtained from the followng monomers and name the polymerisation process in each case. H H H CH3 4 1 3 NH2 H2N 5arrow_forward(4) Describe the synthesis of plastic especially polyethylene, 1,1- dichloroethane, and polyvinyl chloridearrow_forward
- (a) Describe the polymerization of a blend of maleic anhydride and 2-methyl-1,3- propanediol in the presence of an acid catalyst. Draw a chemical reaction scheme showing the intermediate and final products that are formed. Describe the reaction conditions that you would use to maximize the yield of polymer. (b) Draw the structure of the polymer, showing the repeat unit and end groups, that is obtained when the mole ratio of maleic anhydride to diol is 0.95 (c) What is the number average molecular weight of the polymer of Part (b) when the extent of reaction of maleic anhydride is (i) 90% and (ii) 100%. (d) Describe how the structure of the polymer is altered when it is further reacted with styrene in the presence of peroxide.arrow_forwardCan you explain condensation polymerization and give an example with structure of one with 2 carboxylic acid groups and 2 OH groups.arrow_forward(a) What is the empirical formula of cellulose? (b) Whatis the monomer that forms the basis of the cellulose polymer?(c) What bond connects the monomer units in cellulose:amide, acid, ether, ester, or alcohol?arrow_forward
- (a) Hard contact lenses, which first became popular in the 1960s, were made by polymerizing methyl methacrylate [CH; =C(CH,)CO,CH3] to form poly(methyl methacrylate) (PMMA). Draw the structure of PMMA. (b) More comfortable softer contact lenses introduced in the 1970s were made by polymerizing hydroxyethyl methacrylate [CH2=C{CH)CO,CH,CH2OH] to form poly(hydroxyethyl methacrylate) (poly-HEMA). Draw the structure of poly-HEMA. Since neither polymer allows oxygen from the air to pass through to the retina, newer contact lenses that are both comfortable and oxygen-permeable have now been developed.arrow_forwardConsider monomers A–C. (a) Rank the monomers in order of increasing reactivity in cationic polymerization. (b) Rank the monomers in order of increasing reactivity in anionic polymerization.arrow_forwardNeed help with part b,c,darrow_forward
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