diff --git a/src/routes/igcse/chemistry/organic_chemistry/+page.svelte b/src/routes/igcse/chemistry/organic_chemistry/+page.svelte
index 017c53a..b38dc70 100644
--- a/src/routes/igcse/chemistry/organic_chemistry/+page.svelte
+++ b/src/routes/igcse/chemistry/organic_chemistry/+page.svelte
@@ -203,46 +203,77 @@
> while addition polymerisation only produces a polymer.
- Nylon is made from a dicarboxylic acid (a carboxylic acid with two carboxyl -COOH groups) and a
- diamine (an amine with two amine -NH2 groups).
+ Nylon is made from a dicarboxylic acid (a carboxylic acid with two carboxyl -COOH
+ groups) and a diamine (an amine with two amine -NH2 groups).
- - the dicarboxylic acid loses a hydroxyl group (-OH) from each carboxyl group (-C(=O)OH)
- - the diamine loses one hydrogen (-H) from each amine group (-NH2)
+ -
+ the dicarboxylic acid loses a hydroxyl group (-OH) from each carboxyl
+ group (-C(=O)OH)
+
+ -
+ the diamine loses one hydrogen (-H) from each amine group
+ (-NH2)
+
- the hydrogen and hydroxyl combine to form water
-
- the remainder of the dicarboxylic acid, now -(O=)C-R-C(=O)- and the remainder
- of the diamine, now -(H)N-R-N(H)- combine to form a condensation polymer
- [-(O=)C-R-C(=O)N(H)-R-N(H)-]n
+ the remainder of the dicarboxylic acid, now -(O=)C-R-C(=O)-
+ and the remainder of the diamine, now -(H)N-R'-N(H)-
+ combine to form a condensation polymer
+ [-(O=)C-R-C(=O)N(H)-R'-N(H)-]n
Nylon is a polyamide, whereas PET, a polyester, is made from a dicarboxylic acid and a diol (an alcohol
- with two hydroxyl -OH groups).
+ with two hydroxyl-OH groups).
- - the dicarboxylic acid loses a hydroxyl group (-OH) from each carboxyl group (-C(=O)OH)
- - the diol loses one hydrogen (-H) from each hydroxyl group (-OH)
+ -
+ the dicarboxylic acid loses a hydroxyl group (-OH) from each carboxyl
+ group (-C(=O)OH)
+
+ -
+ the diol loses one hydrogen (-H) from each hydroxyl group
+ (-OH)
+
- the hydrogen and hydroxyl combine to form water
-
- the remainder of the dicarboxylic acid, now -(O=)C-R-C(=O)- and the remainder
- of the diol, now -O-R-O- combine to form a condensation polymer [-(O=)C-R-C(=O)O-R-O-]n
+ the remainder of the dicarboxylic acid, now -(O=)C-R-C(=O)-
+ and the remainder of the diol, now -O-R'-O- combine
+ to form a condensation polymer
+
+ [-(O=)C-R-C(=O)O-R'-O-]n
+
Proteins are natural polyamides. These are formed by the condensation polymerisation of amino
- acids, H2N-CHR-COOH (where
+ acids, H2N-CHR-COOH (where
R is any side chain), rather than dicarboxylic acids and diamines.
- While the structure of a synthetic polyamide like nylon looks like this: [-(O=)C-R-C(=O)N(H)-R-N(H)-]n
+ While the structure of a synthetic polyamide like nylon looks like this:
+ [-(O=)C-R-C(=O)N(H)-R'-N(H)-]n
+
- The structure of a polypeptide (protein) looks like this: [-(H)N-R-C(=O)N(H)-R-C(=O)-]n
+ The structure of a polypeptide (protein) looks like this:
+
+ [-(H)N-R-C(=O)N(H)-R'-C(=O)-]n
+
Notice how each monomer unit in a protein has the remanence of an amine group
and of a carboxyl group.
+
+