A polypeptide is also called a polyamide. Nylon is also an example of a polyamide. What is a polyamide? Consider a polyhydrocarbon, a polyester, and a polyamide. Assuming average chain lengths are equal, which polymer would you expect to make the strongest fibers and which polymer would you expect to make the weakest fibers? Explain.

Short Answer

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A polyamide is a polymer containing amide functional groups formed by the reaction of an amine group and a carboxylic acid group. The strengths of polyamide, polyhydrocarbon, and polyester fibers depend on their intermolecular forces. Polyamides have the strongest fibers due to their stronger hydrogen bonding interactions, polyhydrocarbons have the weakest fibers since they rely on weak Van der Waals forces, and polyesters fall in between with stronger fibers than polyhydrocarbons but weaker than polyamides.

Step by step solution

01

Define Polyamide

A polyamide is a type of polymer containing amide functional groups, which are formed by the reaction of an amine group (NH2) and a carboxylic acid group (COOH). These polymers consist of repeating monomers linked by amide bonds. Polypeptides and nylon are common examples of polyamides.
02

Define Polyhydrocarbon

A polyhydrocarbon is a type of polymer consisting of only hydrogen and carbon atoms. These polymers are formed by the reaction of carbon-carbon double bonds in the monomers. Polyethylene and polypropylene are examples of polyhydrocarbons.
03

Define Polyester

A polyester is a type of polymer containing ester functional groups (COO), formed by the reaction of an alcohol group (OH) with a carboxylic acid group (COOH). These polymers consist of repeating monomers linked by ester bonds. Polyethylene terephthalate (PET) is a well-known example of a polyester.
04

Strengths Comparison

To determine the strengths of these fibers, we need to consider the intermolecular forces acting between their polymer chains. Stronger intermolecular forces would lead to stronger fibers. The main types of intermolecular forces are Van der Waals forces, hydrogen bonding, and dipole-dipole interactions. Polyhydrocarbons rely on Van der Waals forces, which are relatively weak. This result in weaker fibers compared to polyamides and polyesters. Polyesters have ester linkages, but the presence of oxygen in the ester groups may lead to some dipole-dipole and/or hydrogen bonding interactions. These interactions are stronger than Van der Waals forces, resulting in stronger fibers than polyhydrocarbons. Polyamides have amide linkages that allow for stronger hydrogen bonding due to the presence of nitrogen atoms with lone pairs of electrons. This leads to stronger intermolecular forces and stronger fibers compared to both polyhydrocarbons and polyesters.
05

Conclusion

Considering the average chain lengths are equal, polyamides would be expected to make the strongest fibers, due to their stronger hydrogen bonding interactions. Polyhydrocarbons would be expected to make the weakest fibers, as they only rely on relatively weak Van der Waals forces. Polyesters would be in the middle, with stronger fibers than polyhydrocarbons but weaker fibers than polyamides.

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Most popular questions from this chapter

Marathon Problems. These problems are designed to incorporate several concepts and techniques into one situation. For each of the following, fill in the blank with the correct response. All of these fill-in-the-blank problems pertain to material covered in the sections on alkanes, alkenes and alkynes, aromatic hydrocarbons, and hydrocarbon derivatives. a. The first "organic" compound to be synthesized in the laboratory, rather than being isolated from nature, was _____________which was prepared from____________. b. An organic compound whose carbon-carbon bonds are all single bonds is said to be______. c. The general orientation of the four pairs of electrons around the carbon atoms in alkanes is_______. d. Alkanes in which the carbon atoms form a single unbranched chain are said to be_______alkanes. e. Structural isomerism occurs when two molecules have the same number of each type of atom but exhibit different arrangements of the_______between those atoms. f. The systematic names of all saturated hydrocarbons have the ending_______ added to a root name that indicates the number of carbon atoms in the molecule. g. For a branched hydrocarbon, the root name for the hydrocarbon comes from the number of carbon atoms in the _________continuous chain in the molecule. h. The positions of substituents along the hydrocarbon framework of a molecule are indicated by the ________of the carbon atom to which the substituents are attached. i. The major use of alkanes has been in_______reactions,as a source of heat and light. J. With very reactive agents, such as the halogen elements, alkanes undergo _______reactions, whereby a new atom replaces one or more hydrogen atoms of the alkane. k. Alkenes and alkynes are characterized by their ability to undergo rapid, complete ______ reactions, by which other atoms attach themselves to the carbon atoms of the double or triple bond. 1\. Unsaturated fats may be converted to saturated fats by the process of ________ m. Benzene is the parent member of the group of hydrocarbons called ________ hydrocarbons. n. An atom or group of atoms that imparts new and characteristic properties to an organic molecule is called a ___________ group. 0.4 _________alcohol is one in which there is only one hydrocarbon group attached to the carbon atom holding the hydroxyl group. p. The simplest alcohol, methanol, is prepared industrially by the hydrogenation of ________ q. Ethanol is commonly prepared by the __________of certain sugars by yeast. r. Both aldehydes and ketones contain the _______group but they differ in where this group occurs along the hydrocarbon chain. s. Aldehydes and ketones can be prepared by _______ of the corresponding alcohol. t. Organic acids, which contain the __________ group, are typically weak acids. u. The typically sweet-smelling compounds called ____________ result from the condensation reaction of an organic acid with an___________.

Integrative Problems. These problems require the integration of multiple concepts to find the solutions. Helicenes are extended fused polyaromatic hydrocarbons that have a helical or screw-shaped structure. a. \(A 0.1450\) -g sample of solid helicene is combusted in air to give \(0.5063 \mathrm{g} \mathrm{CO}_{2}\). What is the empirical formula of this helicene? b. If a \(0.0938-g\) sample of this helicene is dissolved in \(12.5 \mathrm{g}\) of solvent to give a 0.0175 \(M\) solution, what is the molecular formula of this helicene? c. What is the balanced reaction for the combustion of this helicene?

Give the structure for each of the following. a. 3 -hexene b. \(2,4-\) heptadiene c. 2 -methyl- 3 -octene

Draw structural formulas for each of the following alcohols. Indicate whether the alcohol is primary, secondary, or tertiary. a. \(1-\) butanol c. 2 -methyl- 1 -butanol b. 2-butanol d. 2 -methyl- 2 -butanol

Why is it preferable to produce chloroethane by the reaction of HCI(g) with ethene than by the reaction of \(\mathrm{Cl}_{2}(g)\) with ethane? (See Exercise 62.)

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