Organic Chemistry (6th Edition)
Organic Chemistry (6th Edition)
6th Edition
ISBN: 9781260119107
Author: Janice Gorzynski Smith
Publisher: McGraw Hill Education
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Chapter 28.6, Problem 19P
Interpretation Introduction

(a)

Interpretation: The structure of prepolymer A formed from 1,4-dihydroxybenzene and excess epichlorohydrin is to be stated.

Concept introduction: Epoxides are strained three-membered rings. They undergo anionic polymerization to afford the ring opening, by following the SN2 pathway. The ring opening in an unsymmetrical epoxide takes place at the less substituted or the more accessible carbon atom.

Interpretation Introduction

(b)

Interpretation: The structure of cross-linked polymer B formed from the treatment of A with H2NCH2CH2CH2NH2 is to be stated.

Concept introduction: Epoxides are strained three-membered rings. They undergo anionic polymerization to afford the ring opening, by following the SN2 pathway. The ring opening in an unsymmetrical epoxide takes place at the less substituted or the more accessible carbon atom.

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(a) Draw the structure of polystyrene, the chapter-opening molecule, which is formed by polymerizing the monomer styrene, C6H5CH = CH2. (b) What monomer is used to form poly(vinyl acetate), a polymer used in paints and adhesives?
(a) Draw the structure of polystyrene, which is formed by polymerizing the monomer styrene, C6H5CH=CH2. (b) What monomer is used to form poly(vinyl acetate), a polymer used in paints and adhesives?
3. 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.
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