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

Compare the molecular structures of cotton and polypropylene, the two major components of thermal underwear. One of these gets wet easily and holds the water in contact with the skin. The other one does not get wet, but wicks the water away from the skin and feels relatively dry to the touch. Explain the difference in how these two fabrics respond to moisture.

Short Answer

Expert verified

Cotton is made up of cellulose molecules while polypropylene is made up of large number of isopropanes. Cotton becomes wet easily since it has a large number of hydroxide groups. However, polypropylene is practically a hydrocarbon and is considered to be hydrophobic. Hence, it feels relatively dry to touch.

Step by step solution

01

Cellulose (cotton)

It is a polymer of beta glucose. It is the chief structural material of the plants and is obtained from wood and cotton. About 50 % of wood is cellulose. Cellulose contains about 90-95% cellulose. Cellulose is an example of natural polymer.

02

Polypropylene

This type of polymer is formed by the successive addition of monomer units to the growing chain carrying a reactive intermediate such as a free-radical. The most commonly used radical initiator is benzoyl peroxide. Polypropylene is a type of chain-growth polymers (addition polymers).

03

Explanation

Cotton is made up of cellulose molecules while polypropylene is made up of large number of isopropanes. Cotton becomes wet easily since it has a large number of hydroxide groups. However, polypropylene is practically a hydrocarbon and is considered to be hydrophobic. Hence, it feels relatively dry to touch.

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

Show the intermediate that would result if the growing chain added to the other end of the styrene double bond. Explain why the final polymer has phenyl groups substituted on alternate carbon atoms rather than randomly distributed.

Propose a mechanism for the reaction of phenyl isocyanate with methanol.

Chain branching is not as common with anionic polymerization as it is with free-radical polymerization and cationic polymerization.

  1. Propose a mechanism for chain branching in the polymerization of acrylonitrile.
  2. Compare the relative stabilities of the intermediates in this mechanism with those you drew for chain branching in the cationic polymerization of styrene (Problem 26-6). Explain why chain branching is less common in this anionic polymerization.

Olestraยฎis a fat-based fat substitute that became available in snack foods such as potato chips in 1998. Previous fat substitutes were carbohydrate-based or protein-based mixtures that did not give as good a sensation in the mouth and are not suitable for frying. With Olestraยฎ, the glycerol molecule of a fat is replaced by sucrose (p. 1237). In Olestraยฎ, the sucrose molecule has six, seven, or (most commonly) eight fatty acids esterified to its hydroxy groups. The fatty acids come from hydrolysis of vegetable oils such as soybean, corn, palm, coconut, and cottonseed oils. This unnaturally bulky, fat-like molecule does not pass through the intestinal walls, and digestive enzymes cannot get close to the sucrose center to bind it to their active sites. Olestraยฎ passes through the digestive system unchanged, and it provides zero calories.Draw a typical Olestraยฎ molecule, using any fatty acids that are commonly found in vegetable oils.

Kodelยฎ polyester is formed by transesterification of dimethyl terephthalate with 1,4-di(hydroxymethyl)cyclohexane. Draw the structure of Kodel.

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