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
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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
Transcribed Image Text: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:
H₂N
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
X. Poly(caprolactone) - starting monomer at right:
Y. Poly(methyl methacrylate), far right:
Z. Nylon-11 (it's a ring-opening polymerization)
H₂C
CH3
CH3
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