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In referring to the molecular mass of a polymer, we can speak only of the average molecular mass. Explain why the molecular mass of a polymer is not a unique quantity, as it is for a substance like benzene.

Short Answer

Expert verified
The molecular mass of polymers is not unique because they are made up of many repeating units, or monomers, which can vary in number. In contrast, benzene has a fixed formula and structure, resulting in a unique molecular mass.

Step by step solution

01

Understanding Polymers

Polymers are large molecules that are formed by joining together many small molecules called monomers. Due to this process known as polymerization, the molecular mass of a polymer is not fixed because the number of monomer units can vary.
02

Understanding Benzene

On the other hand, benzene (C6H6) is a compound with a fixed formula and structure. It contains 6 carbon and 6 hydrogen atoms, making its molecular mass unique and constant.
03

Contrasting Polymers And Benzene

While the molecular mass of benzene is dependent on its unique molecular formula, the molecular mass of polymers can range from thousands to millions of atomic mass units (amu) because the number of repeating units (monomers) is not constant. This is why we speak of an 'average' molecular mass for polymers.

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Key Concepts

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

Polymers and Monomers
Imagine a train. Each carriage of the train can be seen as a small building block, similar to how monomers are the basic building blocks of polymers. Monomers are small, reactive molecules that have the ability to bond with other monomers to form long chains or networks. These chains, known as polymers, are like trains with varying numbers of carriages.

In nature, polymers occur in many forms such as proteins, which are made of amino acid monomers, and DNA, composed of nucleotide monomers. Synthetic polymers include plastics like polyethylene, which comprises repeated ethylene monomers. Because monomers can be joined together in different numbers and sequences, the resulting polymers vary greatly in size, structure, and properties.
Polymerization Process
Polymerization is akin to building a pearl necklace where each pearl represents a monomer. The process of polymerization involves the chemical linking of these 'pearls' to form a 'necklace,' which in chemistry terms, is the polymer. This can occur in various ways, but the two primary methods are addition polymerization and condensation polymerization.

Addition Polymerization

In this process, monomers add together without the loss of any small molecules. An example of this is the formation of polyethylene.

Condensation Polymerization

This method involves the joining of monomers with the simultaneous elimination of small molecules like water. An instance of this process is the synthesis of nylon. Each method dictates the molecular structure and mass of the resulting polymer.
Average Molecular Mass
When we talk about the size of a polymer, we are usually referring to its molecular mass. However, unlike small, well-defined molecules, polymers consist of a distribution of chains with different lengths, which means they have a range of molecular masses. To address this, scientists use the term 'average molecular mass.'

There are different ways to measure this average, which include the number-average molecular mass, \(M_n\), and the weight-average molecular mass, \(M_w\). \(M_n\) takes into account the total mass of the polymer divided by the total number of molecules, while \(M_w\) is weighted by the mass fraction of each molecular species. Often, these averages are not the same because they signify different aspects of the size distribution within a sample of polymer.
Molecular Formula of Benzene
Diving into organic chemistry, benzene is a fundamental structure with the molecular formula \(C_6H_6\). The molecule is comprised of six carbon atoms arranged in a ring, with one hydrogen atom attached to each carbon.

This arrangement is described as an aromatic ring, a concept essential in understanding many organic compounds. Benzene serves as a building block for a vast range of chemicals, from simple molecules such as phenol to complex pharmaceuticals. The substance's consistent structure means that its molecular mass is always the same, a stark contrast to the variability in the molecular mass of polymers.

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Most popular questions from this chapter

Predict the main product(s) of (a) the mononitration of chlorobenzene; (b) the monosulfonation of nitrobenzene; (c) the monochlorination of 1-methyl-2-nitrobenzene

Indicate the principal product(s) you would expect in (a) treating \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}=\mathrm{CH}_{2}\) with dilute \(\mathrm{H}_{2} \mathrm{SO}_{4}(\mathrm{aq})\) (b) exposing a mixture of chlorine and propane gases to ultraviolet light; (c) heating a mixture of isopropyl alcohol and benzoic acid; (d) oxidizing sec-butyl alcohol with \(\mathrm{Cr}_{2} \mathrm{O}_{7}^{2-}\) in acidic solution.

The reduction of aldehydes and ketones with a suitable hydride-containing reducing agent is a good way of synthesizing alcohols. This approach would be even more effective if, instead of a hydride, we could use a source of nucleophilic carbon. Attack by a carbon atom on a carbonyl group would give an alcohol and simultaneously form a carbon-to-carbon bond. How can we make a C atom in an alkane nucleophilic? This was achieved by Victor Grignard, who created the organometallic reagent \(\mathrm{R}-\mathrm{MgBr},\) with the following reaction in diethyl ether: $$\mathrm{R}-\mathrm{Br}+\mathrm{Mg} \longrightarrow \mathrm{R}-\mathrm{MgBr}$$ The Grignard reagent is rarely isolated. It is formed in solution and used immediately in the desired reaction. The alkylmetal bond is highly polar, with the partial negative charge on the \(\mathrm{C}\) atom, which makes the C atom highly nucleophilic. The Grignard reagent \((\mathrm{R}-\mathrm{MgBr})\) can attack a carbonyl group in an aldehyde or ketone as follows: Addition of dilute aqueous acid solution to the metal alkoxide furnishes the alcohol. The important synthetic consequence of this procedure is that we have prepared a product with more carbon atoms than present in the starting material. A simple starting material can be transformed into a more complex molecule. (a) What is the product of the reaction between methanal and the Grignard reagent formed from 1-bromobutane after the addition of dilute acid? (b) By using a Grignard reagent, devise a synthesis for 2-hexanol. (c) By using a Grignard reagent, devise a synthesis for 2 -methyl- 2 -hexanol. (d) Grignard reagents can also be formed with aryl halides, such as chlorobenzene. What would be the product of the reaction between the Grignard reagent of chlorobenzene and propanone? Can you think of an alternative synthesis of this product, again using a Grignard reagent? (e) The basicity of the \(C\) atom bound to the magnesium in the Grignard reagent can be used to make Grignard reagents of terminal alkynes. Write the equation of the reaction between ethylmagnesium bromide and 1-hexyne. [Hint: Ethane is evolved.] (f) By using a Grignard reagent, suggest a synthesis for 2 -heptyn-1-ol.

How would you synthesize ( \(R\) )-2-butanamine from (S)-2-butanol?

Starting with the compounds chloromethane, chloroethane, sodium azide, sodium cyanide, and a reducing agent, suggest how the following compounds could be synthesized. (a) \(N\) -methylpropanamide (b) ethylethanoate (c) methylethylamine (d) tetramethylammonium chloride

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