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

. Poly (trimethylene carbamate) is used in high-quality synthetic leather. It has the structure shown.

(a) What type of polymer is poly (trimethylene carbamate)?

(b) Is this a chain-growth polymer or a step-growth polymer?

(c) Draw the products that would be formed if the polymer were completely hydrolyzed under acidic or basic conditions.

Short Answer

Expert verified

(a)It is a polyurethane.

(b) As with all polyurethanes, it is a step-growth polymer.


Step by step solution

01

Step-1. Explanation of part (a) and (b):

Poly (trimethylene carbamate) is a polyurethane. Polyurethanes refers to class of polymers which are composed of organic units joined by carbamate links. These are family of plastics, and they are durable, flexible and adaptable.

Poly (trimethylene carbamate) is a step-growth polymer and undergoes step-growth polymerisation in which formation of polymer occurs from bi-functional or multifunctional monomers.

02

Step-2. Explanation of part (c):

Poly (trimethylene carbamate) if completely hydrolysed under acidic or basic conditions, then it would result in the formation of amino alcohol and also carbon-dioxide will get released in this process. Cleavage of nitrogen-carbon bond occurs which gives rise to intermediates and these intermediates rearrange to form amino alcohol and carbon dioxide gas as release of gas increases entropy of the system, thus this process is favourable.

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

Bisphenol A is made on a large scale by a condensation of phenol with acetone. Suggest an appropriate catalyst, and propose a mechanism for this reaction. (Hint: This is a condensation because three molecules are joined with loss of water. The mechanism belongs to another class of reactions though.)

(a) Isobutylene and isoprene coplymerize to give โ€œbutyl rubberโ€. Draw the structure of the repeating unit in butyl rubber, assuming that the two monomers alternate.

(b) Styrene and butadiene copolymerize to form styrene-butadiene rubber (SBR) for automobile tires. Draw the structure of the repeating unit in SBR, assuming that the two monomers alternate.

Poly (vinyl alcohol), a hydrophilic polymer used in aqueous adhesives, is made by polymerizing vinyl acetate and then hydrolyzing the ester linkages.

(a) Give the structures of poly (vinyl acetate) and poly (vinyl alcohol).

(b) Vinyl acetate is an ester. Is poly (vinyl acetate) therefore a polyester? Explain.

(c) We have seen that basic hydrolysis destroys the Dacron polymer. Poly (vinyl acetate) is converted to poly (vinyl alcohol) by a basic hydrolysis of the ester groups. Why doesnโ€™t the hydrolysis destroy the poly (vinyl alcohol) polymer?

(d) Why is poly (vinyl alcohol) made by this circuitous route? Why not just polymerize vinyl alcohol?

Polyoxymethylene (polyformaldehyde) is the tough, self-lubricating DelrinR plastic used in gear wheels.

(a) Give the structure of polyformaldehyde.

(b) Formaldehyde is polymerized using an acidic catalyst. Using H+ as a catalyst, propose a mechanism for the polymerization as far as the trimer.

(c) Is Delrin an addition polymer or a condensation polymer?

The mechanism given for cationic polymerization of isobutylene (Mechanism 26-2) shows that all the monomer molecules add with the same orientation, giving a polymer with methyl groups on alternate carbon atoms of the chain. Explain why no isobutylene molecules add with the opposite orientation.

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