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Ethylene (ethene) is a hydrocarbon. Give the names and structural formulas of two other hydrocarbons that, like ethylene, can serve as monomers.

Short Answer

Expert verified
Propylene \( C_3H_6 \) and Butadiene \( C_4H_6 \) are hydrocarbons that can serve as monomers like ethylene.

Step by step solution

01

Identify ethylene structure

Ethylene, also known as ethene, has the chemical formula \( C_2H_4 \) and consists of two carbon atoms double-bonded to each other, with each carbon atom also bonded to two hydrogen atoms.
02

Understand monomer characteristics

A monomer is a small molecule that can join together with other similar molecules to form a polymer through chemical reactions. Common monomers are typically unsaturated molecules, meaning they have double or triple bonds.
03

Find Propylene

Propylene (or propene) is the first example. It is similar to ethylene but contains three carbon atoms: one of the carbon atoms is double-bonded to another carbon, and this double-bonding allows it to act as a monomer. The chemical formula is \( C_3H_6 \) and its structure is: \( CH_3-CH=CH_2 \).
04

Find Butadiene

Butadiene is the second example. It has four carbon atoms with two double bonds, making it an unsaturated molecule capable of polymerization. The chemical formula is \( C_4H_6 \) and the structure is: \( CH_2=CH-CH=CH_2 \).

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Key Concepts

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

Ethylene
Ethylene, also referred to as ethene, is a basic yet fascinating molecule that sits at the core of many important processes in chemistry. Its simple formula is \( C_2H_4 \). This denotes a structure in which two carbon atoms are linked by a double bond. Each carbon atom is also attached to two hydrogen atoms. The presence of this double bond categorizes ethylene as an "unsaturated" molecule, permitting it to engage in a variety of reactions, including polymerization.
Because of its reactive double bond, ethylene acts as a building block in the creation of other molecules, like plastics and other synthetic materials, through polymerization. This reactivity makes it a versatile compound used widely in industrial chemistry and materials science.
Monomers
Monomers are the fundamental units that link together to form polymers, which are essentially large chains of repeated chemical structures. Think of monomers as the individual beads on a bracelet chain. Each monomer in a polymer is a small, repeating unit that holds the potential to connect with other monomers.
One defining trait of monomers is the presence of unsaturated bonds—either double or triple bonds—which enable them to chemically bind with each other. This binding through chemical reactions occurs in a process called polymerization, where these small entities join to form a long continuous chain, known as a polymer.
Unsaturated Molecules
Unsaturated molecules are characterized by the presence of one or more double or triple bonds between carbon atoms. These types of bonds are crucial because they create points of high reactivity within the molecule. This high reactivity is because these bonds can "open up" and allow other atoms or molecules to attach through various chemical reactions.
Given this attribute, unsaturated molecules can participate in a wide range of chemical reactions. This includes serving as monomers in polymerization processes, where they can connect with other unsaturated molecules to form larger structures. Their unsaturated nature is what makes them excellent candidates for constructing polymers.
Polymerization
Polymerization is the chemical process that transforms monomers into polymers. This fascinating process involves the linking together of individual monomer units to form a larger, more complex structure. It's similar to assembling Legos into an intricate model, where each small piece represents a monomer.
There are different forms of polymerization, including addition and condensation reactions. In the case of compounds like ethylene, addition polymerization is common. Here, the double bonds in unsaturated monomers "open up," allowing them to connect into long chains. The result is a highly durable and flexible polymer, an essential component in creating a myriad of everyday materials, from plastic bags to synthetic rubber.

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Most popular questions from this chapter

Consider Spectra, Allied-Signal Corporation’s HDPE fi ber, used as liners for surgical gloves. Although the Spectra liner has a very high resistance to being cut, the polymer allows a surgeon to maintain a delicate sense of touch. The interesting thing is that Spectra is linear HDPE, which is usually associated with being rigid and not very fl exible. a. Suggest a reason why branched LDPE cannot be used in this application. b. Offer a molecular level reason for why linear HDPE is successful in this application.

Glucose from corn is the source of some new bio-based polymer materials. Glucase also is the monomer in cellulose. Earlier in this text you encountered glucose in the chemical reaction of photosynthesis. What is photosynthesis and from what is glucose produced?

Isoprene is the monomer that forms natural rubber. Here is its structural formula, with the carbons numbered. CH2 C CH CH2 CH3 1 2 3 4 When isoprene monomers add to form polyisoprene (natural rubber), the polymer has a C5C double bond between carbon atoms 2 and 3. How does this double bond form? Hint: Each double bond has four electrons in it. When a new single bond is formed between two monomers, that single bond only needs two electrons in it, one from each of the monomers joined by that new bond.

Many monomers contain a \(\mathrm{C}=\mathrm{C}\) double bond. Select one and draw its structural formula together with the corresponding polymer. Describe the similarities and differences between the monomer and the polymer.

Kevlar is a type of nylon called an aramid. It contains rings similar to that of bennene. Because of its great mechanical strength, Kevlar is used in radial tires and in bulletproof vests. Your Turn \(9.17\) gives the structures for the two monomers, terephthalic acid and phenylenediamine. Name the functional groups in both the monomers and in the polymer.

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