2.3 Review Example 4 in Chapter 2 as a way to reinforce your knowledge of free radical and condensation polymerizations and the types of monomers and polymers used/synthesized in each. Then add 7 new structures to this list by drawing the repeat unit for each of the polymers below: CH CH₂ T. Polyacrylamide - starting monomer: acrylamide, shown at right U. Polyurea - starting monomers: diamine (see part E) and diisocyanate (part Q) V. Polyarylate - starting monomers: terephthalic acid (part C) and bisphenol-A (part N) W. Poly(phenylene sulfide) (PPS) (Ryton", Supec") - starting monomers: para- dichlorobenzene and Na₂S H₂N X. Poly(caprolactone) - starting monomer at right: Y. Poly(methyl methacrylate), far right: Z. Nylon-11 (it's a ring-opening polymerization) H₂C CH3 ge CH3

2.3 Review Example 4 in Chapter 2 as a way to reinforce your knowledge of free radical and condensation polymerizations and the types of monomers and polymers used/synthesized in each. Then add 7 new structures to this list by drawing the repeat unit for each of the polymers below: CH CH₂ T. Polyacrylamide - starting monomer: acrylamide, shown at right U. Polyurea - starting monomers: diamine (see part E) and diisocyanate (part Q) V. Polyarylate - starting monomers: terephthalic acid (part C) and bisphenol-A (part N) W. Poly(phenylene sulfide) (PPS) (Ryton", Supec") - starting monomers: para- dichlorobenzene and Na₂S H₂N X. Poly(caprolactone) - starting monomer at right: Y. Poly(methyl methacrylate), far right: Z. Nylon-11 (it's a ring-opening polymerization) H₂C CH3 ge CH3

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter8: Haloalkanes, Halogenation, And Radical Reactions

Section: Chapter Questions

Problem 8.34P

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