Chapter 27 Amines, Amides And Condensation Polymers Flashcards
What is addition polymerisation?
Reactions between monomers with multiple bonds (e.g. C=C double bonds) to form saturated polymers (without double bonds)
A small molecule is not eliminated
What is condensation polymerisation?
Monomers react to form a polymer with the elimination of a smaller molecule
What are secondary amines?
Amines with two alkyl / aryl groups attached
What are the different ways you can form polyamides?
Amino acid + amino acid
Diamine + decarboxylic acid
Diamine + diacyl chloride
What are the bonds between amino acids called?
Peptide linkages
What are the different ways you can form polyesters?
Diol + dicarboxylic acid
Diol + diacyl chloride
Hydroxycarboxylic acid + hydroxycarboxylic acid
What are the conditions and reagents needed to form a primary amine and WHY?
ETHANOL solvent to prevent haloalkane reacting with water to form alcohol
EXCESS AMMONIA to prevent further REDUCTION of primary amine to form secondary amine
+ NaOH later on to remove halogen group to leave primary amine behind
What is an example of the reactants needed to form a primary amine?
CH3Cl + NH3 -> CH3NH3+Cl-
CH3NH3+Cl- + NaOH -> CH3NH2 + NaCl + H2O
What is an example of the reactants needed to form a secondary amine?
CH3Cl + CH3NH2 -> (CH3)2NH2+Cl-
(CH3)2NH2+Cl- + NaOH -> (CH3)2NH2 + NaCl + H2O
What are zwitterions?
Ions containing both a negatively charged group and a positively charged group on the same atom
What is an example of a zwitterion?
a-amino acids
E.g. alanine
What is the isoelectric point?
pH at which a zwitterion contains both a negatively charged group and a negatively charged group
What is an optical isomer?
Non-superimposable mirror images of a compound
How do zwitterions work?
Placed in solution with HIGHER pH (alkaline) than isoelectric point = acts as ACID and DONATES proton
Placed in solution with LOWER pH (acidic) than isoelectric point = acts as BASE and ACCEPTS proton
What is a racemic mixture?
A mixture containing 50% left-hand optical isomers and 50% right-hand optical isomers