Skip to ContentGo to accessibility page
Organic Chemistry

31.3 Copolymers

Organic Chemistry31.3 Copolymers

31.3 Copolymers

31.3 • Copolymers

Up to this point we’ve discussed only homopolymers—polymers that are made up of identical repeating units. In practice, however, copolymers are more important commercially. Copolymers are obtained when two or more different monomers are allowed to polymerize together. For example, copolymerization of vinyl chloride with vinylidene chloride (1,1-dichloroethylene) in a 1 : 4 ratio leads to the polymer Saran.

Copolymerization of monomer mixtures often leads to materials with properties quite different from those of either corresponding homopolymer, giving the polymer chemist a vast flexibility for devising new materials. Table 31.1 lists some common copolymers and their commercial applications.

Table 31.1 Some Common Copolymers and Their Uses
Monomers Structures Trade name Uses
Vinyl chloride
Vinylidene chloride
Saran Fibers, food packaging
Styrene
1,3-Butadiene
SBR (styrene–butadiene rubber) Tires, rubber articles
Hexafluoropropene
Vinylidene fluoride
Viton Gaskets, seals
Acrylonitrile
1,3-Butadiene
Nitrile rubber Adhesives, hoses
Isobutylene
Isoprene
Butyl rubber Inner tubes
Acrylonitrile
1,3-Butadiene
Styrene
ABS (monomer initials) Pipes, high-impact applications

Several different types of copolymers can be defined, depending on the distribution of monomer units in the chain. If monomer A is copolymerized with monomer B, for instance, the resultant product might have a random distribution of the two units throughout the chain, or it might have an alternating distribution.

The exact distribution of monomer units depends on the initial proportions of the two reactant monomers and their relative reactivities. In practice, neither perfectly random nor perfectly alternating copolymers are usually found. Most copolymers have many random imperfections.

Two other forms of copolymers that can be prepared under certain conditions are called block copolymers and graft copolymers. Block copolymers are those in which different blocks of identical monomer units alternate with each other; graft copolymers are those in which homopolymer branches of one monomer unit are “grafted” onto a homopolymer chain of another monomer unit.

Block copolymers are prepared by initiating the polymerization of one monomer as if growing a homopolymer chain and then adding an excess of the second monomer to the still-active reaction mix. Graft copolymers are made by gamma irradiation of a completed homopolymer chain in the presence of the second monomer. The high-energy irradiation knocks hydrogen atoms off the homopolymer chain at random points, thus generating new radical sites that can initiate polymerization of the added monomer.

Problem 31-6
Draw the structure of an alternating segment of butyl rubber, a copolymer of isoprene (2-methyl-1,3-butadiene) and isobutylene (2-methylpropene) prepared using a cationic initiator.
Problem 31-7
Irradiation of poly(1,3-butadiene), followed by addition of styrene, yields a graft copolymer that is used to make rubber soles for shoes. Draw the structure of a representative segment of this styrene–butadiene graft copolymer.
Citation/Attribution
Reuse and redistribution of this content in digital or print format:
  • This book may not be used in the training of large language models or otherwise be ingested into large language models or generative AI offerings without OpenStax's prior written permission.
  • This book uses the Creative Commons Attribution-NonCommercial-ShareAlike License, which means that you can reuse and modify the material only for noncommercial purposes, must attribute OpenStax, and must distribute any derivative works under the same license.
  • Any commercial printing of this textbook, including using a local or custom printer, must be approved by OpenStax, and proper citation provided.
  • OpenStax-copyrighted images, activities, assessments, and similar components of this book are subject to the same licensing – CC-BY-NC-SA. They can be used for noncommercial purposes with attribution. Commercial use requires permission.
  • Permission requests: Anyone who intends to incorporate this content (including text, images, and other components) into large language models, use it in AI offerings, use it commercially (including in print), and/or has questions about another use case is welcome to complete our reuse request form.
Attribution information
  • If you are redistributing all or part of this book in a noncommercial print format, then you must include on every physical page the following attribution:

    Access for free at https://openstax.org/books/organic-chemistry/pages/1-why-this-chapter

  • If you are redistributing all or part of this book in a noncommercial digital format, then for every page that includes OpenStax content, you must license the derivative work under the same CC-BY-NC-SA license as the original, and include on every digital page view the following attribution:

    Access for free at https://openstax.org/books/organic-chemistry/pages/1-why-this-chapter

Citation information

The information below includes the information needed to generate citations in most major styles (APA, MLA, etc.); you must reformat and organize the information as needed to fit the requirements of the style. Use the information below to generate a citation. We recommend using a citation tool such as this one.

© Jul 1, 2026 OpenStax. Textbook content produced by OpenStax is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike License. The OpenStax name, OpenStax logo, OpenStax book covers, OpenStax CNX name, and OpenStax CNX logo, and Rice University name, and Rice University logo trademarks, or wordmarks are not subject to the Creative Commons license and may not be reproduced without the prior and express written consent of Rice University.