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

Polystyrene can be made more rigid by copolymerizing styrene with divinylbenzene: How does the divinylbenzene make the copolymer more rigid?

Short Answer

Expert verified
The divinylbenzene makes the copolymer more rigid by forming cross-links between the polymer chains due to the presence of its two vinyl groups. This creates a more interconnected and rigid network structure in the copolymer, resulting in increased rigidity and durability compared to polystyrene alone.

Step by step solution

01

Understand copolymerization

Copolymerization is a process where two or more different monomers (small molecules) are chemically combined to form a polymer (a large molecule composed of repeating units). In this case, we want to understand the copolymerization of styrene and divinylbenzene, and how this process makes the resultant copolymer more rigid.
02

Analyze the structure of styrene and divinylbenzene

Styrene is a monomer with the chemical formula C8H8. Its structure consists of a benzene ring with a vinyl group (CH=CH2) attached to it. Divinylbenzene, on the other hand, is similar to styrene but has two vinyl groups attached to the benzene ring, with the formula C10H10.
03

Understand the impact of divinylbenzene on the copolymer

When styrene and divinylbenzene are copolymerized, the resultant copolymer has a more complex structure than that of polystyrene alone. The presence of two vinyl groups in the divinylbenzene molecule allows it to form cross-links between the polymer chains, creating a more interconnected and rigid network structure in the copolymer.
04

Conclusion

The addition of divinylbenzene to styrene during the copolymerization process results in the formation of a more rigid copolymer. This is because the divinylbenzene molecules can form cross-links between the polymer chains, allowing for a more interconnected and rigid network structure in the copolymer. This increased rigidity can be beneficial in various applications, such as in the production of more rigid and durable plastic materials.

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

Draw a structural formula for each of the following compounds. a. 2 -methylpropane b. 2 -methylbutane c. 2 -methylpentane d. 2 -methylhexane

Choose one of the following terms to match the description given in statements (1)-(17). All of the following pertain to proteins or carbohydrates. a. aldohexose g. disaccharides \(\mathbf{m}\). ketohexoses b. saliva h. disulfide n. oxytocin c. cellulose i. globular o. pleated sheet d. \(\mathrm{CH}_{2} \mathrm{O}\) j. glycogen p. polypeptide e. cysteine \(\mathbf{k}\). glycoside linkage q. primary structure f. denaturation 1\. hydrophobic (1) polymer consisting of many amino acids (2) linkage that forms between two cysteine species (3) peptide hormone that triggers milk secretion (4) proteins with roughly spherical shape (5) sequence of amino acids in a protein (6) silk protein secondary structure (7) water-repelling amino acid side chain (8) amino acid responsible for permanent wave in hair (9) breakdown of a protein's tertiary and/or secondary structure (10) animal polymer of glucose (11) \(-\mathrm{C}-\mathrm{O}-\mathrm{C}-\) bond betwecn rings in disaccharide sugars (12) empirical formula leading to the name carbohydrate (13) where enzymes catalyzing the breakdown of glycoside linkages are found (14) six-carbon ketone sugars (15) structural component of plants, polymer of glucose (16) sugars consisting of two monomer units (17) six-carbon aldehyde sugars

The base sequences in mRNA that code for certain amino acids are Glu: \(\quad\) GAA, GAG Val: GUU, GUC, GUA, GUG Met: \(\quad\) AUG Trp: \(\quad\) UGG Phe: UUU, UUC Asp: \(\quad\) GAU, GAC These sequences are complementary to the sequences in DNA. a. Give the corresponding sequences in DNA for the amino acids listed above. b. Give a DNA sequence that would code for the peptide trp-glu-phe-met. c. How many different DNA sequences can code for the tetrapeptide in part \(\mathrm{b}\) ? d. What is the peptide that is produced from the DNA sequence \(\mathrm{T}-\mathrm{A}-\mathrm{C}-\mathrm{C}-\mathrm{T}-\mathrm{G}-\mathrm{A}-\mathrm{A}-\mathrm{G} ?\) e. What other DNA sequences would yield the same tripeptide as in part \(\mathrm{d}\) ?

Draw a structural formula for each of the following. a. 3-methylpentanoic acid b. ethyl methanoate c. methyl benzoate d. 3 -chloro- 2,4 -dimethylhexanoic acid

Give two examples of saturated hydrocarbons. How many other atoms are bonded to each carbon in a saturated hydrocarbon?

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