ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5
ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5
2nd Edition
ISBN: 9780393664034
Author: KARTY
Publisher: NORTON
Question
Book Icon
Chapter 11, Problem 11.55P
Interpretation Introduction

Interpretation:

The detailed mechanism that illustrates the initiation and addition of the first two monomers in the given polymerization reaction is to be drawn.

Concept introduction:

Polymerization reactions start with the generation of a reactive species from a monomer molecule. The reactive species may be a radical or a carbocation. This reactive species then adds to another molecule of the monomer to form a dimer. At the same time, a radical or a carbocation is generated on the added molecule, which can continue the addition reaction.

In the case of acid-catalyzed alkene polymerization, a proton transfer from the acid to a molecule of alkene generates a carbocation reactive species. This in turn acts as an electrophile and adds to the double bond from another monomer molecule, generating a second, dimeric carbocation. This carbocation will then propagate the polymerization reaction.

Blurred answer
Students have asked these similar questions
Macromolecules can also be formed from cyclic monomers such as cyclic hydrocarbons, ethers, esters, amides, siloxanes, and sulfur (eight-membered ring). Thus, ring-opening polymerization is of particular interest, since macromolecules of almost any chemical structure can be prepared. Choose two of the above type polymers to explain the mechanism and chemical reaction of polymerization process.
One common type of cation exchange resin is prepared by polymerization of a mixture containing styrene and 1,4-divinylbenzene  . The polymer is then treated with concentrated sulfuric acid to sulfonate a majority of the aromatic rings in the polymer. Q.) Explain how this sulfonated polymer can act as a cation exchange resin
Can you explain condensation polymerization and give an example with structure of one with 2 carboxylic acid groups and 2 OH groups.

Chapter 11 Solutions

ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5

Knowledge Booster
Background pattern image
Recommended textbooks for you
  • Text book image
    Chemistry: The Molecular Science
    Chemistry
    ISBN:9781285199047
    Author:John W. Moore, Conrad L. Stanitski
    Publisher:Cengage Learning
    Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305580350
    Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
    Publisher:Cengage Learning
    Text book image
    Principles of Modern Chemistry
    Chemistry
    ISBN:9781305079113
    Author:David W. Oxtoby, H. Pat Gillis, Laurie J. Butler
    Publisher:Cengage Learning
  • Text book image
    Chemistry: Principles and Reactions
    Chemistry
    ISBN:9781305079373
    Author:William L. Masterton, Cecile N. Hurley
    Publisher:Cengage Learning
    Text book image
    World of Chemistry, 3rd edition
    Chemistry
    ISBN:9781133109655
    Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
    Publisher:Brooks / Cole / Cengage Learning
    Text book image
    Chemistry
    Chemistry
    ISBN:9781133611097
    Author:Steven S. Zumdahl
    Publisher:Cengage Learning
Text book image
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Text book image
Principles of Modern Chemistry
Chemistry
ISBN:9781305079113
Author:David W. Oxtoby, H. Pat Gillis, Laurie J. Butler
Publisher:Cengage Learning
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781133611097
Author:Steven S. Zumdahl
Publisher:Cengage Learning