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A chain growth copolymer is (a) terylene (b) neoprene (c) nylon-6 (d) SBR

Short Answer

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a) Terylene b) Neoprene c) Nylon-6 d) SBR (styrene-butadiene rubber) Answer: b) Neoprene and d) SBR (styrene-butadiene rubber)

Step by step solution

01

Review the definition of a chain growth copolymer

A chain growth copolymer is a type of copolymer that forms through a step-growth polymerization mechanism. In this process, monomers with reactive functional groups react with one another to form longer chains. The polymer chains grow in a sequential manner, with one monomer unit reacting with another until the polymer reaches its desired length.
02

Compare the given options with the definition of a chain growth copolymer

Now, let's analyze each option and determine if it is a chain growth copolymer. (a) Terylene is a polyester formed through a condensation polymerization mechanism between ethylene glycol and terephthalic acid. This reaction is not a chain growth polymerization process, so Terylene is not a chain growth copolymer. (b) Neoprene is a type of synthetic rubber that forms through a free radical polymerization of chloroprene. This is a chain growth process, making Neoprene a chain growth copolymer. (c) Nylon-6 is a type of polyamide that forms through a polycondensation reaction between amino acids or lactams. This process does not involve a chain growth polymerization mechanism, so Nylon-6 is not a chain growth copolymer. (d) SBR (styrene-butadiene rubber) is formed through a free radical polymerization mechanism of the monomers styrene and butadiene. This is a chain growth process, making SBR a chain growth copolymer as well.
03

Identify the chain growth copolymers among the given options

Based on our analysis, both Neoprene (option b) and SBR (option d) are examples of chain growth copolymers.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Polymerization Mechanism
Polymerization is a chemical process where small molecules, known as monomers, join together to form larger chains or networks called polymers. There are two primary mechanisms for polymerization: chain growth and step growth. In chain growth polymerization, individual monomer units add to a growing chain one at a time. This type of polymerization is characterized by three distinct stages: initiation, propagation, and termination. The process begins with the formation of reactive intermediates that help add monomers in a sequential manner.
Step growth polymerization, on the other hand, involves the bonding of monomers that contain complementary functional groups, leading to the formation of small oligomers that gradually combine to form larger polymer structures. Understanding the differences between these mechanisms is crucial, as they influence the properties and applications of the resulting polymers.
Free Radical Polymerization
Free radical polymerization is a common chain growth polymerization method where free radicals, which are atoms or molecules with unpaired electrons, initiate the polymerization process. These free radicals are often generated through the thermal decomposition or chemical reaction of certain initiator compounds.
This mechanism works in three main steps: initiation, where the free radical is formed; propagation, where the radical adds to a monomer to create a new radical site, continuing the chain reaction; and termination, where two radicals combine or a radical reaction is stopped, thus ending chain growth.
  • Suitability: It's particularly useful for polymerizing vinyl and styrene-based monomers.
  • Sensitivity: The reaction is sensitive to oxygen as it can quench the free radicals, stopping the polymerization process prematurely.
This method is employed in the production of common polymers like polyvinyl chloride (PVC) and polystyrene.
Synthetic Rubber
Synthetic rubber refers to artificial elastomers produced through polymerization techniques. Unlike natural rubber, which is derived from latex found in plants, synthetic rubber is manufactured using various chemical processes.
It is predominantly created through free radical polymerization, often yielding materials like neoprene and styrene-butadiene rubber (SBR). These materials offer excellent resistance to temperature variations and mechanical stress, making them suitable for a range of applications, including automotive tires and industrial gaskets. Consider the following when looking at synthetic rubber:
  • Versatility: Can be engineered to have particular qualities required for specific uses.
  • Durability: Generally more durable against environmental factors compared to natural rubber.
This adaptability and resilience make it a crucial material in countless industries, upgrading the performance of various products.
Polycondensation Reaction
Polycondensation is an essential polymerization process where monomers react by eliminating small molecules like water or methanol to form a polymer. Unlike chain growth polymerization, polycondensation involves a slow step-wise bonding of monomers, forming bolomers and eventually long chains.
Products of polycondensation reactions include polyamides, polyesters, and other materials that have high strength and thermal resistance. This process is significant in producing everyday materials such as Nylon-6 and Terylene, which are used in textiles and plastics.
Key aspects to understand about polycondensation include:
  • Byproducts: Each bonding step releases a small molecule, which needs to be removed effectively.
  • Temperature and Pressure: Conditions are crucial to ensure the successful removal of byproducts and to achieve the desired molecular weight.
Thus, this reaction is foundational in producing high-performance materials utilized across a broad spectrum of industries.

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Most popular questions from this chapter

Synthetic polymers are classified by their sequence of synthesis as chain growth or step growth polymers. Chain growth polymers are produced by chain reaction polymerization in which an initiator adds to a carbon-carbon double bond of a vinyl monomer to yield a reactive intermediate. The intermediate reacts with a second monomer to yield a new intermediate which reacts with a third unit and so on. The initiator may be a radical or an acid or an anion. Acid catalysed polymerization is effective in case of vinyl monomers having electron donating groups. Anionic polymerization requires the presence of electron withdrawing groups. One of the important catalysts used in polymerization is Ziegler-Natta catalyst (triethyl aluminium and titanium tetrachloride). One of the important aspects of Zeiglar-Natta catalysed polymers is that they are stereo-chemically controllable. Three forms (i) isotactic (ii) syndiotactic and (iii) atactic can be produced Vinylidene chloride \(\mathrm{H}_{2} \mathrm{C}=\mathrm{CCl}_{2}\) does not polymerize in isotactic, syndiotactic or atactic forms because (a) it contains electronegative chlorine atoms. (b) it has sp \(^{2}\) hybridized carbon. (c) it is a planar molecule. (d) the polymer formed has no chiral centre

State whether the following statements are true or false? (i) Glucose is the only aldose that shows mutarotation. (ii) The smallest aldose to form a hemiacetal is a tetrose. (iii) a-D-glucose \(\rightleftharpoons\) aldehyde form \(\rightleftharpoons\) b-D- glucose. This conversion is known as mutarotation. (iv) The anomers of D-glucose have specific rotations of same magnititude but opposite sign. (v) Sucrose is a 1,4 '-glycoside. (vi) In alkaline medium, fructose is a reducing sugar. (vii) Cellobiose is a polysaccharide. (viii) Natural sugar has D-configuration.

Give the sequence of reactions when D-glucose reacts with excess of \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{NHNH}_{2}\) in the presence of acetic acid?

This section contains multiple choice questions. Each question has 4 choices (a), (b), (c) and (d), out of which ONLY ONE is correct. Percentage of \(\alpha\) -D-glucose in the equilibrium mixture with its anomer in aqueous solution is (a) 64 (b) \(52.5\) (c) 36 (d) 32

This section contains multiple choice questions. Each question has 4 choices (a), (b), (c) and (d), out of which ONLY ONE is correct. . Which of the following have \(\alpha\) -glycosidic linkages? (i) starch (ii) cellobiose (iii) lactose (iv) maltose (v) cellulose (a) (i), (ii) and (iv) (b) (ii), (iii) and (v) (c) (i) and (iv) (d) (i), (iv) and (v)

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