describe the formation of polyesters: (a) the reaction between a diol and a dicarboxylic acid or dioyl chloride (b) the reaction of a hydroxycarboxylic acid
describe the formation of polyamides: (a) the reaction between a diamine and a dicarboxylic acid or dioyl chloride (b) the reaction of an aminocarboxylic acid (c) the reaction between amino acids
deduce the repeat unit of a condensation polymer obtained from a given monomer or pair of monomers
identify the monomer(s) present in a given section of a condensation polymer molecule
Source: Cambridge International syllabus · แหล่งที่มา: หลักสูตร Cambridge International
English
In condensation polymerisation 缩合聚合, monomers join into a long chain and a small molecule (such as water or $\text{HCl}$) is lost each time a new bond forms. Each monomer needs two reactive groups, so the chain can grow at both ends.
Polyesters
A polyester 聚酯 has many ester links along its chain. You can make one from:
a diol 二醇 (two $\text{–OH}$ groups) and a dicarboxylic acid 二羧酸 (two $\text{–COOH}$ groups), or a dioyl chloride.
a single hydroxycarboxylic acid, which has both an $\text{–OH}$ and a $\text{–COOH}$.
Polyamides
A polyamide 聚酰胺 has many amide links. You can make one from:
a diamine 二胺 (two $\text{–NH}_2$ groups) and a dicarboxylic acid or a dioyl chloride.
a single aminocarboxylic acid, or from amino acids 氨基酸 joining together (proteins are natural polyamides).
Repeat units and monomers
The repeat unit 重复单元 of a condensation polymer contains parts of both monomers, minus the atoms lost as the small molecule. To find the monomers 单体 from a section of polymer, break the chain at each ester or amide link, then add back $\text{–OH}$ and $\text{–H}$ (or $\text{–Cl}$).
Worked example. A polymer chain contains repeating $\text{–CONH–}$ links. Name the type of polymer, identify the monomers, and give the small molecule lost. A $\text{–CONH–}$ link is an amide, so this is a polyamide made by condensation polymerisation. To find the monomers, break the chain at each amide link and give the cut ends their atoms back: the carbon side takes $\text{–OH}$, making a dicarboxylic acid, and the nitrogen side takes $\text{–H}$, making a diamine. The small molecule lost at each link is water (or $\text{HCl}$, if an acyl dichloride was used in place of the acid). Each monomer must have two functional groups, or the chain could never keep growing - if the monomer you propose has only one, you have broken the chain in the wrong place.
Source: Cambridge International syllabus · แหล่งที่มา: หลักสูตร Cambridge International
English
poly(alkene)s 聚烯烃 are chemically inert — they have only strong, non-polar C–C and C–H bonds, so they are hard to biodegrade 可生物降解 and last a long time.
some polymers are made so that light can break them down (they are photodegradable).
polyesters and polyamides are biodegradable, because their ester and amide links can be broken by acidic or alkaline hydrolysis 水解.
Condensation polymers (polyesters, polyamides) form with loss of a small molecule ($\text{H}_2\text{O}$ or HCl) — draw the repeat unit and the lost molecule.
Identify the monomers from the polymer by breaking the ester or amide link — a common question.
Predict the type from the monomers: a $\text{C}=\text{C}$ gives addition; two functional groups give condensation.
Polyesters and polyamides are hydrolysable (more degradable); addition polymers are not.
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