1) Correctly name the following organic compounds. Identify each compound above as an ether, ester, 1o, 2o or 3o amine or 1o, 2o or 3o amide.
a) 2-methoxymethylpropane b) ethoxycyclohexane c) isopropylbutanoate d) phenylethanoate e) N-ethyl-methyl-1-propanamine f) N,N-dimethylethanamine
g) 3-propoxypentane h) 3-methylpentanamide i) N-ethylbenzamide j) butylbenzoate k) N-ethyl-N,3-dimethyl-2-pentanamine l) 2-methyl-1,3-cyclopentanediamine
m) N,3-diethyl-N-propylpentanamide n) N-isopropylethanamide o) N-phenylethanamide
2) Reactants required: ethanol + benzoic acid, using sulfuric acid catalyst for dehydration synthesis:
3) Reactants required: ethanol using sulfuric acid catalyst for dehydration synthesis:
4) Orlon:
5) Polyvinyl alcohol (PVA):
6) Saran Wrap:
7) Lexan:
8) Dacron:
9) Polypeptide chain:
10)
|
|
|
|
|
|
|
methane |
CH4 |
alkanes |
LDF |
-164 |
|
methanoic acid |
HCOOH |
carboxylic acids |
H-bonding |
100.7 |
|
methanol |
CH3OH |
alcohols |
H-bonding |
65 |
|
methylmethanoate |
HCOOCH3 |
esters |
dipole-dipole |
31.5 |
|
methanamine |
CH3NH2 |
amines |
H-bonding |
-6 |
|
methoxymethane |
CH3OCH3 |
ethers |
dipole-dipole |
-25 |
11) Draw the structural formula for the following compounds: org_review_formulae.JPG
12) Complete the following reactions and name the organic reactants and products:
Rxns (a) to (g): org_rxns_a_to_g.JPG
Rxns (h) to (l): org_rxns_h_to_l.JPG