Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

How does a condensation polymer differ from an addition polymer? Give an example of each.

Short Answer

Expert verified
Condensation polymers are formed from monomers reacting together with the elimination of a small molecule, usually water, and involve reactions between functional groups like alcohols, carboxylic acids, or amines. An example is polyester formed from the reaction between a dicarboxylic acid and a diol. Addition polymers are formed by the addition reaction of unsaturated monomers containing carbon-carbon double bonds, with no elimination of small molecules. An example of an addition polymer is polyethylene, formed by the polymerization of ethylene.

Step by step solution

01

Define condensation polymers and addition polymers

Condensation polymers are formed from monomers reacting together with the elimination of a small molecule, usually water. Addition polymers are formed by the addition reaction of unsaturated monomers without the elimination of any molecule.
02

Explain the formation mechanism of condensation polymers

The formation of condensation polymers involves reactions between functional groups present on the monomers, such as alcohol, carboxylic acid, or amine groups. During the polymerization process, a covalent bond is formed between the two monomers, and a small molecule, such as water or methanol, is eliminated. This process continues, linking the monomers together into a polymer chain. Example: Polyester is a type of condensation polymer formed by the reaction between a dicarboxylic acid (e.g., terephthalic acid) and a diol (e.g., ethylene glycol). The carboxylic acid and alcohol groups on the monomers react to form ester linkages, eliminating water molecules in the process. \[ HOOC-R_1-COOH + HO-R_2-OH \rightarrow [-OC-R_1-COO-R_2-O-]_n + (n-1)H_2O \]
03

Explain the formation mechanism of addition polymers

Addition polymers are formed by the polymerization of unsaturated monomers containing carbon-carbon double bonds. During the polymerization process, the double bond of the monomer is broken, and new carbon-carbon single bonds are formed with other monomers. In contrast to condensation polymerization, there is no elimination of any small molecules during the formation of addition polymers. Example: Polyethylene is an example of an addition polymer formed by the polymerization of ethylene (ethene), which is an unsaturated hydrocarbon with a carbon-carbon double bond. \[ nCH_2=CH_2 \rightarrow [-CH_2-CH_2-]_n \]
04

Summary

In summary, condensation polymers are formed by reactions between monomers with the elimination of a small molecule, usually water, while addition polymers are formed by the addition reaction of unsaturated monomers with no elimination of small molecules. Examples of a condensation polymer and an addition polymer are polyester and polyethylene, respectively.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Polymerization Process
Polymerization is a chemical process that connects small molecules known as monomers into long, repeating chains to form polymers. There are several methods by which polymers can be synthesized, but the two primary types are condensation polymerization and addition polymerization.

In condensation polymerization, monomers react and join together with the simultaneous loss of small molecules like water or methanol. This is well represented in the production of polyester, where the elimination of water is part of forming the ester linkage that gives the polyester its structure. A simple representation of this reaction is as such: \[ HOOC-R_1-COOH + HO-R_2-OH \rightarrow [-OC-R_1-COO-R_2-O-]_n + (n-1)H_2O \].

On the other hand, in addition polymerization, unsaturated monomers (typically containing double bonds) link up without the loss of any other atoms or molecules. The monomers simply add to one another in a chain-growth fashion, as seen in the polymerization of ethylene to form polyethylene, showcased by the equation: \[ nCH_2=CH_2 \rightarrow [-CH_2-CH_2-]_n \].

Both types of polymerization are crucial in the production of various synthetic materials that we use in everyday life.
Monomers and Polymers
Understanding the relationship between monomers and polymers is central to grasping the basics of polymer science. Monomers are small, simple molecules that serve as the building blocks of polymers. They can join with other monomers, often in repeated sequences, to form complex and larger molecules known as polymers.

Take for instance, the monomers of ethylene glycol and terephthalic acid in the production of polyester. These monomers react through their functional groups – an alcohol and a carboxylic acid respectively – to form polyester chains while releasing water.

Similarly, the monomer ethylene undergoes addition polymerization to become polyethylene. The carbon-carbon double bond in ethylene is key as it opens up to link with other ethylene molecules, forming the long chains characteristic of polymers.

Essentially, monomers are the alphabets that make up the words (polymers), and the polymerization process is like forming sentences from these words to create a meaningful narrative – in this case, materials with diverse properties and applications.
Chemical Structure of Polymers
The chemical structure of polymers determines their properties and functions. Polymers consist of long chains of atoms, primarily carbon, hydrogen, and sometimes other elements like oxygen, nitrogen, and sulfur. The arrangement of these atoms in the chain, the type of monomers involved, and the nature of the bonds connecting these monomers define the polymer’s characteristics.

Condensation polymers such as polyesters have a characteristic structure with ester linkages. The repeated unit in the chain often contains a part from both reacting monomers interlinked by an ester bond, as shown in the reaction for polyester synthesis. This arrangement imparts properties like strength and flexibility to the material.

For addition polymers like polyethylene, the chains consist of carbon atoms linked by single bonds, and the simplicity of the repeating -CH2- units imparts properties like toughness and plasticity. These polymers often exhibit high resistance to chemicals and electrical insulation properties due to their saturation and the absence of reactive double bonds.

A polymer's molecular weight, degree of branching, and cross-linking also play crucial roles in determining its mechanical strength, elasticity, and other physical properties.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

What commercial chemical reactions of terephthalic acid would be used to give a common polyester?

When formaldehyde is polymerized to a linear polymer in heptane solvent, with \(\left(\mathrm{C}_{6} \mathrm{H}_{5}\right){ }_{3} \mathrm{P}\) or a proton as a catalyst, it yields a thermally unstable material (A) that unzips readily to re-form formaldehyde. However, if the end of the polymer is 'capped", the product is a highly crystalline, tough polymer. The example below, \(\mathrm{B}\), is called Delrin and is already replacing nylon as a molding resin. Suggest a reason for the stability gained by capping the polymer.

High-pressure polyethylene differs from polyethylene, made with the aid of Ziegler catalysts, in having a lower density and lower \(\mathrm{T}_{\mathrm{m}} .\) It has been suggested that this is due to branches in the chains of the high-pressure material. Explain how such branches might arise in the polymerization process and how they would affect the density and \(\mathrm{T}_{\mathrm{m}}\).

A sample of styrene is polymerized with the help of a little azoisobutyronitrile as initiator. Hydrolysis of the resulting polymer releases \(6 \mathrm{~g}\) of ammonia from \(10 \mathrm{~kg}\) of polymer. If all the end groups are derived from the initiating radical ( \(\alpha\) cyanoisopropyl), what is the average number of styrene units in the chain?

Apparently the economically important chain reaction, wool \(+\) moths \(\rightarrow\) holes \(+\) more moths, has, as a key step, scission of the disulfide linkages of cystine in the polypeptide chains by the digestive enzymes of the moth larva. Devise a method of mothproofing wool which would involve chemically altering the disulfide linkages

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free