Sigma Percentile
JEE Advanced 2019
LEVELJEE Main

Animated Solution for Chemistry - Polymers: Choose the correct option(s) from the following

Select Answer:

* Multiple Correct

Visualized Solution

Analyzing the Options

  • We need to evaluate four statements regarding the structure and synthesis of common polymers: Natural Rubber, Nylon-6, Cellulose, and Teflon.

Option A: Natural Rubber

  • Natural rubber is a polymer of isoprene (2-methyl-1,3-butadiene).
  • The double bonds in the polymer chain have a cis configuration.
  • Therefore, it is cis-1,4-polyisoprene.

Option B: Nylon-6

  • Nylon-6 is synthesized from the monomer caprolactam.
  • It is a polyamide, meaning its polymer chain contains amide linkages ().

Option C: Cellulose

  • Cellulose is a straight-chain polysaccharide composed entirely of -D-glucose units.
  • These units are joined by -1,4-glycosidic linkages.
  • Starch, on the other hand, contains -D-glucose units.

Option D: Teflon

  • Teflon (Polytetrafluoroethylene) is prepared by heating tetrafluoroethene ().
  • The reaction requires high pressure and a free radical catalyst like persulphate.

Final Conclusion

  • Correct Statements:
  • (B) Nylon-6 has amide linkages.
  • (D) Teflon is prepared by heating tetrafluoroethene with a persulphate catalyst at high pressure.

The Sigma Insight: Classification of Polymers

Solution Diagram

Demystifying Polymer Structures

A Deep Dive into Natural Rubber, Nylon-6, Cellulose, and Teflon
When tackling questions on polymers in competitive exams like JEE, success often hinges on your ability to recall specific structural details, monomers, and the types of linkages that hold the polymer chains together. Let's break down the four statements provided in this question to understand exactly why each is either correct or incorrect.

Analyzing Natural Rubber

The first statement claims that natural rubber is polyisoprene containing trans alkene units. While it is true that natural rubber is a polymer of isoprene (2-methyl-1,3-butadiene), the geometric configuration of the double bonds in the polymer chain is strictly cis.
This cis-1,4-polyisoprene structure prevents the polymer chains from packing closely together, which is precisely what gives natural rubber its characteristic elasticity. If the double bonds were in the trans configuration, the chains would pack tightly, forming a hard, non-elastic material known as gutta-percha. Therefore, statement (A) is incorrect.

Analyzing Nylon-6

The second statement asserts that Nylon-6 has amide linkages. Nylon-6 is synthesized by heating caprolactam with water at high temperatures. Caprolactam is a cyclic amide containing six carbon atoms.
During polymerization, the ring opens up, and the molecules link together to form a long chain. Because the monomer itself contains an amide group, the resulting polymer chain is held together by repeating amide linkages (). This makes Nylon-6 a polyamide, confirming that statement (B) is absolutely correct.

Analyzing Cellulose

The third statement suggests that cellulose consists of -D-glucose units. Cellulose is indeed a straight-chain polysaccharide and a major structural component of plant cell walls. However, it is composed exclusively of -D-glucose units joined by -1,4-glycosidic linkages.
It is starch (specifically amylose and amylopectin) that is made up of -D-glucose units. The difference between the and anomers might seem small, but it drastically changes the physical properties of the polymer. The linkages allow cellulose to form strong, rigid fibers, whereas linkages cause starch to coil. Thus, statement (C) is incorrect.

Analyzing Teflon

The final statement describes the preparation of Teflon. Teflon, chemically known as polytetrafluoroethylene (PTFE), is manufactured by the addition polymerization of tetrafluoroethene gas ().
This reaction is carried out under high pressure and requires a free radical initiator to kickstart the polymerization process. A commonly used initiator for this reaction is a persulphate catalyst, which decomposes to provide the necessary free radicals. This perfectly aligns with the description given, making statement (D) correct.

Conclusion

By carefully evaluating the structural chemistry and synthesis conditions of these common polymers, we can confidently conclude that the correct options are (B) and (D).

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