FLOW CHART OF REACTIONS BETWEEN ALKANE, ALKENE, ALCOHOL, CARBOXYLIC ACID AND ESTER
Naming of Carbon compound (Prefix)
No. of carbon Prefix Example Formula 1C Meth Methane CH 4 2C Eth Ethanol C 2 H 5 OH 3C Prop Propene C 3 H 6 4C But Butanoic acid C 3 H 7 COOH 5C Pent Pentane C 5 H 12 6C Hex Hexene C 6 H 12 7C Hept Heptanol C 7 H 15 OH 8C Oct Octanoic acid C 7 H 15 COOH 9C Non Nonane C 9 H 20 10C Dec Decene C 10 H 20
6 characteristics of Homologous series (1) Members can be represented by a same general formula. (2) Members can be prepared using similar methods. (3) Members show a gradual change in their physical properties. (4) Members have similar chemical properties. (5) Members have same functional group. (6) Successive member differ by CH2 group and RMM of 14.
Definition 1. Hydrocarbons are organic compounds that contain the elements carbon and hydrogen only. 2. Saturated hydrocarbon is hydrocarbon that have only single covalent bonds between all the carbon atoms in the molecules. 3. Unsaturated hydrocarbon is hydrocarbon that have at least one carbon-carbon multiple bond in the molecule. 4. The molecular formula is a chemical formula that shows the actual numbers of atoms of each element present in one molecule of the substance. 5. The structural formula of an organic compound is the chemical formula that shows the arrangement of atoms and covalent bonds between atoms in a molecule of the compound. 6. A homologous is a family of organic compounds with the same functional group and with similar chemical properties. 7. A functional group is an atom or a group of atoms that determines the characteristic properties of an organic compound. 8. Isomerism is the existence of two or more compounds that have the same molecular formula but different structural formulae. 9. Isomers are compounds which have the same molecular formula but different structural formulae. Each isomer has a different arrangement of atoms in space. ETHANE C 2 H 6 Chloroethane CH 3 CH 2 Cl + HCl Cl 2
Sunlight /uv Substitution reaction ETHENE C 2 H 4 H 2
Nickel / platinum 200 o C Hydrogenation reaction HCl gas r.t.p
ETHANOL C 2 H 5 OH Steam, Phosphoric acid, H 3 PO 4
300 o C / 60 atm Hydration reaction Br 2 in tetrachloromethane 1, 2-dibromoethane CH 2 BrCH 2 Br Halogenation reaction 200 o C, 1500 atm Addition polymerisatio i) Aluminium oxide/hot porcelain ii) Concentrated H 2 SO 4 , 180 o C iii) Concentrated H 3 PO 4 , 80 o C Ethane-1,2-diol CH 2 OHCH 2 OH Acidified KMnO 4 Dehydration reaction Oxidation reaction i) Acidified potassium dichromate(VI), K 2 Cr 2 O 7 ii) Acidified potassium manganate(VII), KMnO 4 Ethanoic acid CH 3 COOH Ethyl ethanoate CH 3 COOC 2 H 5 Concentrated H 2 SO 4
Hot Alumina Cracking Reaction ALKANE C n H 2n + 2 ALKENE C n H 2n ALCOHOL C n H 2n + 1 ESTER C n H 2n + 1 COOC m H 2m + 1 1. Neutralisation reaction salt and water CH 3 COOH + NaOH CH 3 COONa + H 2 O 2. With active metals (Mg, Zn, Al) salt + H 2 gas 2 CH 3 COOH + Mg (CH 3 COO) 2 Mg + H 2 3. With metallic carbonate salt + CO 2 + H 2 O 2 CH 3 COOH + CaCO 3
(CH 3 COO) 2 Ca + CO 2 + H 2 O
Addition reaction poly(ethene) ( CH 2 CH 2 ) n Number of Isomer Isomers have different physical properties because they have different molecular structural. However, isomers have the same chemical properties because they belong to the same homologous series. Homologo us Series No. of carbon No. of isomer Structural formula 4 Butane 2
;
Alkane 5 Pentane 3
; ;
4 Butene 3
; ;
Alkene 5 Pentene 5 ; ;
3 Propanol 2 ; Alcohol 4 Butanol 4 ; ; ;
C-C-C-C C-C-C-C-C C=C-C-C C-C=C-C C=C-C-C-C C-C=C-C-C C-C-C C C-C-C-C C C C-C-C C C=C-C C C=C-C-C C C=C-C-C C C-C-C OH C-C-C OH C-C-C-C OH C-C-C-C OH C C-C-C OH C C-C-C OH All carbon compound combust in excess oxygen to CO2 and H2O Alkene burns with more sooty flame than corresponding alkane due to higher % of carbon by mass. To differentiate alkane and alkene: Method Observation Add bromine water, Br 2 Alkene decolourise the brown colour of bromine water. Alkane no visible change. Add acidified potassium manganate(VII), KMnO 4
Alkene decolourise the purple colour of KMnO 4 . Alkane no visible change.
position of alkyl parent position of suffix of alkyl group group chain functional group homologous series Name of carbon compounds C 2 H 4 + H 2 O C 2 H 5 OH C 2 H 5 OH + 2[O] CH 3 COOH + H 2 O C 2 H 4 + HCl C 2 H 5 Cl C 2 H 4 + H 2 O + [O] CH 2 OHCH 2 OH C 2 H 4 + Cl 2 CH 2 ClCH 2 Cl C 2 H 5 OH C 2 H 4 + H 2 O C 2 H 4 + H 2 C 2 H 6
C 2 H 6 + Cl 2 C 2 H 5 Cl + HCl C 6 H 12 O 6 2C 2 H 5 OH + 2 CO 2
C 2 H 5 OH + CH 3 COOH CH 3 COOC 2 H 5 + H 2 O n C 2 H 4 (CH 2 CH 2 ) n