The structures of three monomers are shown. In each case, show the structure of the polymer that would result from polymerization of the monomer. Vinyl chloride is polymerized to ‘’vinyl’’ plastics and PVC pipe. Tetrafluoroethylene polymerizes to Teflon, used as non-stick coatings and PTFE valves and gaskets. Acrylonitrile is polymerized to Orlon, used in sweaters and carpets.

Vinyl chloride tetrafluoroethylene acrylonitrile

Short Answer

Expert verified

Polyvinyl chloride, PVC


Polytetrafluoroethylene, PTFE, Teflon

Polyacrylonitrile, Orlon

Step by step solution

01

Addition polymerization

Addition polymerisation is a reaction in which the reaction of monomers leads to formation of polymer without any by-product formation. In free-radical polymerization, addition of a monomer occurs to an active chain-end and gets regenerated. Initiation, propagation, and termination are the basic three steps of the free-radical polymerisation reaction.

02

Polymerization of Polyvinyl chloride, PVC

Vinyl chloride undergoes addition polymerisation reaction to produce polyvinylchloride polymer. PVC is used in drainage pipes, cable and wire insulations etc.

03

Polymerization of Polytetrafluoroethylene, PTFE, Teflon

Tetrafluoroethylene undergoes free radical vinyl polymerisation reaction to produce polytetrafluoroethylene polymer or Teflon. PTFE is used to make gaskets because of its heat resistance and strength.

04

Polymerization of acrylonitrile

Polyacrylonitrile or Orlon is a synthetic resin prepared by free radical vinyl polymerisation of acrylonitrile monomer. PAN is used to make carbon fibre and fibres of PAN have also been used in sails of yachts.

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!

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

Predictthe major products of the following reactions.

a. E- 3-methyloct-3-ene+ ozone, then Me3S

b. Z- 3-methyloct-3-ene+ ozone, then Me3S

e. 1-ethylcycloheptene + ozone, then Me2S

f. 1-ethylcycloheptene + warm, then KMnO4

g. 1-ethylcycloheptene + cold,, dil.KMnO4

Limonene is one of the compounds that give lemons their tangy odour.Show the structures of the products expected when limonene reacts with an excess of each of these reagents.

(a) Borane in tetrahydrofuran, followed by basic hydrogen peroxide

(b) m-chloroperoxybenzoic acid

(c) ozone, then dimethyl sulfide

(d) a mixture of osmic acid and hydrogen peroxide

(e) hot, concentrated potassium permanganate

(f) peroxyacetic acid in acidic water

(g) hydrogen and a platinum catalyst

(h) hydrogen bromide gas

(i) hydrogen bromide gas in a solution containing dimethyl peroxide

(j) bromine water

(k) chlorine gas

(l) mercuric acetate in methanol, followed by sodium borohydride

(m) CHBr3 and 50% aq. NaOH

Predict the major products of the following reactions.

(a) Propene + BH3 .THF (b) the product from part (a) + H2O2/OH-

(c) 2-methylpent-2-ene + BH3.THF (d) the product from part (c) + H2O2/OH-

(e) methylcyclohexane+ BH3 .THF (f) the product from (e) + H2O2/OH-

Propose a mechanism for the addition of bromine water to cyclopentene, being carefulto show why the trans product results and how both enantiomers are formed.

Unknown X, C5 H9 Br, does not react with bromine or with dilute KMnO4. Upon treatment with potassium tert-butoxide, X gives only one product, Y, C5 H8. Unlike X, Y decolorizes bromine and changes KMnO4 from purple to brown. Catalytic hydrogenation of Y gives methylcyclobutane. Ozonolysis–reduction of Y gives dialdehyde Z, C5 H8 O2. Propose consistent structures for X, Y, and Z. Is there any aspect of the structure of X that is still unknown?

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