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

Suppose that you start with a diisocyanate and a diol. Show how their reaction can lead to a polymer called a polyurethane (Section 29.5D).

Short Answer

Expert verified
Answer: The reaction between a diisocyanate and a diol results in the formation of urethane linkages. As the reaction continues, multiple urethane linkages form long chains, connecting the R1 and R2 chains in the diisocyanate and diol molecules. This leads to the formation of a polyurethane polymer with the general structure ...-O=C=N-R1-O-R2-O-...

Step by step solution

01

Define diisocyanates and diols

Diisocyanates are compounds with two functional isocyanate groups (-N=C=O) in their structure, while diols are compounds with two hydroxyl groups (-OH) in their structure.
02

Display the general structure of a diisocyanate and a diol

Let's represent the diisocyanate and diol with general structures. A general diisocyanate can be represented by the following structure: O=C=N-R1-N=C=O and a general diol can be represented by the following structure: HO-R2-OH where R1 and R2 are the carbon chains or other groups connecting the functional groups in each molecule.
03

Show the reaction between the diisocyanate and the diol

When the diisocyanate and diol react, the hydroxyl group of the diol (-OH) reacts with the isocyanate group of the diisocyanate (-N=C=O), forming a urethane linkage. The reaction can be represented as follows: O=C=N-R1-N=C=O + HO-R2-OH -> O=C=N-R1-O-R2-OH + O=C=N-R1-N=C=O Here, one urethane linkage is formed, and the other isocyanate group is still available to react with another diol molecule.
04

Obtain the structure of the resulting polyurethane

As the reaction continues, the isocyanate groups keep reacting with more diol molecules, creating long chains of urethane linkages and connecting the R1 and R2 chains, which forms the polyurethane polymer. In general, the structure of the polyurethane polymer would look like this: ...-O=C=N-R1-O-R2-O-... This is the result of the reaction between a diisocyanate and a diol, leading to a polyurethane polymer.

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

Following is a retrosynthetic analysis for the synthesis of the herbicide (S)-Metolachlor from 2-ethyl-6-methylaniline, chloroacetic acid, acetone, and methanol. Show reagents and experimental conditions for the synthesis of Metolachlor from these four organic starting materials. Your synthesis will most likely give a racemic mixture. The chiral catalyst used by Novartis for reduction in Step 2 gives \(80 \%\) enantiomeric excess of the \(S\) enantiomer.

Draw a structural formula for each compound. (a) Dimethyl carbonate (b) Benzonitrile (c) Isopropyl 3-methylhexanoate (d) Diethyl oxalate (e) Ethyl (Z)-2-pentenoate (f) Butanoic anhydride (g) Dodecanamide (h) Ethyl 3-hydroxybutanoate (i) Octanoyl chloride (j) Diethyl cis-1,2-cyclohexanedicarboxylate (k) Methanesulfonyl chloride (l) \(p\)-Toluenesulfonyl chloride

Nicotinic acid, more commonly named niacin, is one of the B vitamins. Show how nicotinic acid can be converted to (a) ethyl nicotinate and then to (b) nicotinamide. Nicotinic acid Ethyl nicotinate Nicotinamide (Niacin)

Using your roadmaps as a guide, show how to convert 1-bromopentane and sodium cyanide into \(N\)-hexylhexanamide. You must use 1-bromopentane and sodium cyanide as the source of all carbon atoms in the target molecule. Show all reagents and all molecules synthesized along the way.

Using your roadmaps as a guide, show how to convert 1-bromopropane and carbon dioxide into 4-propyl-4-heptanol. You must use 1-bromopropane and carbon dioxide as the source of all carbon atoms in the target molecule. Show all reagents and all molecules synthesized along the way.

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