SPM Chemistry Form 5 ± Terminology and Concepts: Carbon Compounds 1.

Organic compounds ± carbon containing compounds with covalent bonds. 2. Inorganic compounds ± non-living things and usually do not contain carbon but few carbon containing inorganic compounds such as CO2, CaCO3 and KCN. 3. Hydrocarbons ± organic compounds that contain hydrogen and carbon atom only. 4. Non-hydrocarbons ± organic compounds that contain other elements (oxygen, nitrogen, iodine, phosphorus) 5. Saturated hydrocarbons ± only single bonded (Carbon-Carbon) hydrocarbons. 6. Unsaturated hydrocarbons ± at least one double / triple bonded (Carbon-Carbon) hydrocarbons. 7. Complete combustion ± organic compounds burn completely which form CO2 and H2O. Example: C2H5OH (l) + O2 (g) ±> 2CO2 (g) + 3H2O (l) 8. Incomplete combustion ± organic compounds burn with limited supply of O2 which form C (soot), CO, CO2 and H2O. Homologous Series Homologous series ± organic compounds with similar formulae and properties. It have thephysical properties that change gradually as the number of carbon atoms in a molecule increases. General Formula Carbon Compounds Alkane CnH2n+2 n = 1, 2, 3, « Functional group

Carbon-carbon single bond -C±CCarbon-carbon double bond -C=CCarbon-carbon triple bond -C=C-C=Cdelocalised / free to move around the ring

Alkene

CnH2n

n = 2, 3, 4, «

Alkynes

CnHn

n = 2, 3, 4, «

Arenes

CnH2n-6

n = 6, 7, 8, «

Alcohol

CnH2n+1OH

n = 1, 2, 3, «

Hydroxyl group - OH Carboxyl group - COOH Carboxylate group - COO -

Carboxylic Acids Esters

CnH2n+1COOH

n = 0, 1, 2

CnH2n+1COOCmH2m+1 n = 0, 1, 2, « m = 1, 2, 3, «

Sources of Hydrocarbon: 1. Coal ± from the lush vegetation that grew in warm shallow coastal swamps or dead plantsslowly become rock. Mainly contains of hydrocarbon and some sulphur and nitrogen. It is used to produce: fertiliser, nylon, explosives and plastics. 2. Natural gas ± from plants and animals and trapped between the layers of impervious rocks (on top of petroleum). Mainly contains of methane gas and other gas such as propane andbutane. It is used for: cooking, vehicle and generate electrical power. 3. Petroleum ± from plants and animals and trapped between the layers of impervious rocks. It is a complex mixture of alkanes, alkenes, aromatic hydrocarbons and sulphurcompound. These compounds can be separated by using fractional distillation. 
      

< 35°C ± petroleum gas 35°C ± 75°C ± Petrol (gasoline) 75°C ± 170°C ± Naphtha 170°C ± 230°C ± Kerosene 230°C ± 250°C ± Diesel 250°C ± 300°C ± Lubricating oil 300°C ± 350°C ± Fuel oil > 350°C ± Bitumen

More than one side chains are present. Two or more types of branches are present. . name them in alphabetical order. prefixes are used. « (n = number of carbon) Formula CH3 C2H5 C3H7 C4H9 C5H11 Branch or name of group methyl ethyl propyl butyl pentyl 2. Alkyl group signifies that it is not part of the main chain. 3. General formula: CnH2n+1 ±Where n = 1. 2. 1. Organic compound is divided into three portions which is Prefix + Root + Suffix. Prefix ± name of the branch or side chain. Number of side chain 2 3 4 5 6 Prefix DiTriTetraPentaHexa- 4.A) IUPAC (International Union of Pure and Applied Chemistry) ± is used to nameorganic compound. 3.

8. Identify the number of carbon. Example: 4-methylhept-2-ene.5. Homologous series Functional group Suffix Alkane Alkene Alcohol Carboxylic acid Ester -C±C-C=C± OH ± COOH ± COO ± -ane -ene -ol -oic -oate 7. 6. Prefix + Root + Suffix . Suffix ± functional group. Number of carbon atoms 1 2 3 4 5 6 7 8 9 10   Root name methethpropbutpenthexheptoctnandec- The longest continuous (straight chain) carbon chain is selected. Root ± the parent hydrocarbon (denotes the longest carbon chain).

B) Family of Hydrocarbon ± Alkane 1. « (n = number of carbon) 2. 2. 3. Example: molecular formula of butane is C4H2´4+2 = C4H10 . Alkanes are saturated hydrocarbon. Name of alkane Methane Ethane Propane Butane Pentane Hexane Heptane Octane Nonane Decane Molecular formula of alkane CH4 C2H6 C3H8 C4H10 C5H12 C6H14 C7H16 C8H18 C9H20 C10H22 Molecular formula is a chemical formula that shows the actual number of atoms of each type of elements present in a molecule of the compound. Each carbon atom in alkanes is bonded to four other atoms by single covalent bonds. General formula: CnH2n+2 Where n = 1.

3.66 0.68 0. Physical properties of alkanes Name Molecularformula RMM Density(g Physical state at cm-3) 25°C 0.63 0.Name Methane Ethane Propane Butane Pentane Hexane Heptane Octane Nonane Decane Condensed structural formula of alkane CH4 CH3CH3 CH3CH2CH3 CH3CH2CH2CH3 CH3CH2CH2CH2CH3 CH3CH2CH2CH2CH2CH3 CH3CH2CH2CH2CH2CH2CH3 CH3CH2CH2CH2CH2CH2CH2CH3 CH3CH2CH2CH2CH2CH2CH2CH2CH3 CH3CH2CH2CH2CH2CH2CH2CH2CH2CH3 Structural formula is a chemical formula that shows the atoms of elements are bonded(arrangement of atoms) together in a molecule by what types of bond.70 Gas Gas Gas Gas Liquid Liquid Liquid Liquid Methane Ethane Propane Butane Pentane Hexane Heptane Octane CH4 C2H6 C3H8 C4H10 C5H12 C6H14 C7H16 C8H18 16 30 44 58 72 86 100 114 .

Example: Alkanes react with bromine vapour (or chlorine) in the presence of UV light. When going down the series.Nonane Decane C9H20 C10H22 128 142 0. Alkanes are covalent compounds and do not contain freely moving ions. Chemical properties of alkanes  Reactivity of alkanes Alkanes are less reactive (saturated hydrocarbon). Density of alkane ± the density of water is higher than density of alkane. Alkanes do not react with chemicals such as oxidizing agents.73 Liquid Liquid Alkanes with more than 17 carbon atoms are solid. Alkanes have strong carbon-carbon (C ± C) bonds and carbon-hydrogen (C ± H) bonds. reducing agents.72 0. Electrical conductivity ± all members in alkanes do not conduct electricity.   .    4. Combustion of alkanes Complete combustion of hydrocarbons CxHy + (x + y/4) O2 ±> xCO2 + y/2 H2O CH4 + 2O2 ±> CO2 + 2H2OIncomplete combustion occurs when insufficient supply of oxygen CH4 + O2 ±> C + H2O 2CH4 + 3O2 ±> 2CO + 4H2O Substitution reaction of alkanes (Halogenation) Substitution reaction is one atom (or a group of atoms) in a molecule is replaced by another atom (or a group of atoms). relative molecular mass of alkanes is higher due to the higher force of attraction between molecules and alkane molecules are packed closer together. Alkanes are held together by weak intermolecular forces. Boiling and melting points ± all alkanes in general have low boiling points and melting points. Substitution reaction of alkanes take place in ultraviolet light. All are single bonds which require a lot of energy to break. acids and alkalis.  Solubility in water ± all members in alkanes are insoluble in water but soluble in many organic solvent (benzene and ether).

Example: molecular formula of butene is C4H2x4 = C4H8 . Name of alkene Ethene Propene Butene Pentene Hexene Heptene Octene Nonene Decene  Molecular formula of alkene C2H4 C3H6 C4H8 C5H10 C6H12 C7H14 C8H16 C9H18 C10H20 Molecular formula is a chemical formula that shows the actual number of atoms of eachtype of elements present in a molecule of the compound. 3. General formula: CnH2n Where n = 2.CH4 + Cl2 ±> HCl + CH3Cl (Chloromethane) CH3Cl + Cl2 ±> HCl + CH2Cl2 (Dichloromethane) CH2Cl2 + Cl2 ±> HCl + CHCl3 (Trichloromethane) CHCl3 + Cl2 ±> HCl + CCl4 (Tetrachloromethane) The rate of reaction between bromine and alkanes is slower than the rate of reaction between chlorine and alkanes. Family of Hydrocarbon ± Alkene 1. 4 « (n = number of carbon) 2. The functional group in alkenes is carbon-carbon double (C = C) bond. Alkenes are unsaturated hydrocarbons which contain one or more carbon-carbon (C = C) double bonds in molecules. 3.

0011 0.6750 0. Hence.0023 0. Alkenes are held together by weak attractive forces between molecules (intermolecular forces) van der Waals¶ force. more energy is required to overcome the attraction. Density of alkene ± the density of water is higher than density of alkene. When going down the series.7430 Gas Gas Gas Liquid Liquid Liquid Liquid Liquid Liquid Ethene Propene Butene Pentene Hexene Heptene Octene Nonene Decene  C2H4 C3H6 C4H8 C5H10 C6H12 C7H14 C8H16 C9H18 C10H20 28 42 56 70 84 98 112 126 140 Solubility in water ± all members in alkenes are insoluble in water but soluble in many organic solvent (benzene and ether). relative molecular mass of alkenes is higher due to the higher force of attraction between molecules and alkene molecules are packed closer together.6980 0. the boiling and melting points increases.    . When going down the series. Boiling and melting points ± all alkenes in general have low boiling points and melting points. Alkenes are covalent compounds and do not contain freely moving ions.4.0018 0. Electrical conductivity ± all members in alkenes do not conduct electricity.7160 0. Physical properties of alkenes Name Molecularformula RMM Density(g Physical state at cm-3) 25°C 0.7310 0.6430 0.

Addition of halogen (Halogenation) Halogenation is the addition of halogens to alkenes (no catalyst of ultraviolet light is needed). Chemical properties of alkenes  Reactivity of alkenes Alkenes are more reactive (unsaturated hydrocarbon). Polymerisation is small alkene molecules (monomers) are joined together to form a long chain (polymer).CH2 ± CH2 -)-n ethene (monomer)(unsaturated compound) ±> polyethene polymer (saturated compound) It must be carry out in high temperature and pressure. Alkenes have carbon-carbon (C = C) double bonds which is more reactive than carboncarbon (C-C) single bonds. It is because the percentage of carbon in alkene molecules is higher than alkane molecules and alkenes burn plenty of oxygen to produce carbon dioxide and water)  Incomplete combustion occurs when insufficient supply of oxygen C2H4 + O2 ±> 2C + 2H2O C2H4 + 2O2 ±> 2CO + 2H2O (The flame in the incomplete combustion of alkenes is more smoky than alkanes)  Polymerisation reaction of alkenes Polymers are substances that many monomers are bonded together in a repeating sequence. nCH2 = CH2 ±> -(. Combustion of alkenes Complete combustion of hydrocarbons (alkenes) CxHy + (x + y/4) O2 ±> xCO2 + y/2 H2O C2H4 + 3O2 ±> 2CO2 + 2H2O (Alkenes burn with sootier flames than alkanes. Addition of hydrogen (Hydrogenation) Addition reaction is atoms (or a group of atoms) are added to each carbon atom of a carbon-carbon multiple bond to a single bond.5.   . Alkene + Halogen ±> Dihaloalkane C2H4 + Br2 ±> C2H4Br2 In this reaction the brown colour of bromine decolourised (immediately) to produce acolourless organic liquid. All the reaction occur at the double bonds. C2H4 + H2 ±> C2H6 (catalyst: nickel and condition: 200°C) Example: margarine (produce from hydrogenation of vegetable oils).

 Addition of hydrogen halides Hydrogen halides (HX) are hydrogen chlorine. The products are 1bromopropane and 2-bromopropane). Also used to identify the presence of a carbon-carbon double bond in a chemical test. It can react with a mixture ofalkene and steam pass over a catalyst (Phosphoric acid. H3PO4).   . CnH2n + HX ±> CnH2n+1X C2H4 + HBr ±> C2H5Br (Bromoethane) (There are two products for additional of hydrogen halide to propene. Addition of water (Hydration) Alkenes do not react with water under ordinary condition. The product is an alcohol. hydrogen bromide.Bromination is also used to identify an unsaturated (presence of a carbon-carbon double bond) organic compound in a chemical test. This reaction takes place rapidly in room temperature and without catalyst. KMnO4 CnH2n + [O] + H2O ±> CnH2n(OH)2 C2H4 + [O] + H2O ±> C2H5(OH)2 The purple colour of KMnO4 solution decolourised immediately to produce colourlessorganic liquid. hydrogen iodide and etc. CnH2n + H2O ±> CnH2n+1OH C2H4 + H2O ±> C2H5OH Additional of acidified potassium manganate(VII).

Same with alkanes. Reaction with bromine solution No reaction. Electrical conductivity. Boiling points and melting points Do not conduct electricity Same with alkanes.Comparing (Similarities and Differences) Properties of Alkanes and Alkenes Physical Properties Physical state Alkanes Alkenes Physical state changes from gas to liquid when going down the series. Insoluble in water (soluble Same with alkanes. Alkenes (Addition reaction) Reactive Burn in air and produce yellow and sootier flame compare to alkanes. in organic solvent) Alkanes (Substitution reaction) Unreactive Burn in air and produce yellow sooty flame. Decolourise purple acidified potassium manganate(VII) solution. carbon atom per molecule increases). at any state. Reaction with acidified potassium manganate(VII) solution . Low densities (number of Same with alkanes. Decolourise brown bromine solution. Low boiling points and melting points (number of carbon atoms per molecule increases). Same with alkanes. Density Solubility in water Chemical Properties Reactivity Combustion No reaction.

Isomerism Isomerism ± phenomenon that two or more molecules are found to have the same molecular formula but different structural formulae.2.(no isomer) .(no isomer) 2 Structure name Methane Ethane Propane Butane2methylpropane Pentane2methylbutane2.(no isomer) .2dimethylpropane C5H12 3 Isomerism in alkenes Molecular formula C2H4 C3H6 C4H8 Number of isomers .(no isomer) 3 Structure name Ethene Propene But-1-eneBut-2-ene2methylpropene Pent-1-enePent-2-ene2methylbut-1-ene 3-methylbut-1-ene 2-methylbut-2-ene C5H10 5 .(no isomer) . Isomerism in alkanes Molecular formula CH4 C2H6 C3H8 C4H10 Number of isomers .

Name of alcohol Molecular formula of alcohol CH3OH C2H5OH C3H7OH C4H9OH C5H11OH C6H13OH Methanol Ethanol Propanol / Propan-1-ol Butanol / Butan-1-ol Pentanol / Pentan-1-ol Hexanol / Hexan-1-ol Heptanol / Heptan-1-ol C7H15OH Octanol / Octan-1-ol Nonanol / Nonan-1-ol Decanol / Decan-1-ol C8H17OH C9H19OH C10H21OH 4. The functional group in alcohols is hydroxyl group. Alcohols are non-hydrocarbons which contain carbon. ± OH. 2.Non-Hydrocarbon ± Alcohol 1. 3 « (n = number of carbon) 2. General formula: CnH2n + 1OH  Where n = 1. hydrogen and oxygen atoms. Physical properties of alcohol Name Molecular formula CH3OH C2H3OH C3H5OH C4H7OH C5H9OH Melting Boiling Physical state at point (°C) point (°C) 25°C -97 -117 -127 -90 -79 65 78 97 118 138 Liquid Liquid Liquid Liquid Liquid Methanol Ethanol Propanol Butanol Pentanol . 3.

Other example: C3H7OH ±> C3H6 + H2O   6. C2H5OH + 3O2 ±> 2CO2 + 3H2O (Alcohol burns with clean blue flames. toiletries. Boiling and melting points ± all alcohols in general have low boiling points (78°C). CnH2n+1OH ±> CnH2n + H2O C2H5OH ±> C2H4 + H2O Two methods are being used to carry out a dehydration in the laboratory. Therefore. explosives. Chemical properties of alcohol  Combustion of alcohol Complete combustion of alcohol. 7. fiber). Alcohol as a fuel (fuel for racing car. varnishes. b) Ethanol is heated under reflux at 180°C with excess concentrated sulphuric acid. This reaction releases a lot of heat. Colour and Smell ± alcohols are colourless liquid and have sharp smell. Alcohol burns plenty of oxygen to produce carbon dioxide and water.    5. rubbing alcohol). it is a clean fuel as it does not pollute the air. alternative fuel). two common oxidising agents are used for the oxidation of ethanol which are acidified potassium dichromate(VI) solution (orange to green) and acidified potassium manganate(VII) solution (purple to colourless). Alcohol as a source of medical product (antiseptics for skin disinfection. Uses of Alcohol     Alcohol as a solvent (cosmetics. Other example: C3H7OH + 2[O] ±> C2H5COOH + H2O Removal of water (Dehydration) Alcohol can change to alkene by removal of water molecules (dehydration). unglazed porcelain chips. Alcohol as a source of chemicals (polymer. clean fuel. a) Ethanol vapour is passed over a heated catalyst such asaluminium oxide. C2H5OH + 2[O] ±> CH3COOH + H2O Ethanol oxidised to ethanoic acid (a member of the homologous series of carboxylic acids ± will be discussed in Part 6). H2SO4. Solubility in water ± all members in alcohol are very soluble in water (miscible with water). Misuse and Abuse   Depressant drug Alcoholic drinks. thinners. Volatility ± all alcohols are highly volatile. perfumes).) Other example: 2C3H7OH + 9O2 ±> 6CO2 + 8H2O Oxidation of ethanol In the laboratory. vinegar. pumice stone or porous pot. Addictive drugs . It results in the formation of a C=C double bond.

3. Density of carboxylic acid ± density of carboxylic acid increases due to the increases in the number of carbon atoms in a molecule. Boiling points ± all carboxylic acid in general have relatively high boiling points than the corresponding alkanes. 2. hydrogen and oxygen atoms. Carboxylic acid (>10 carbons) are wax-like solids. This is due to the presence of carboxyl group in carboxylic acid. 1. The functional group in alcohols is carboxyl group. 3 « (n = number of carbon) 2. Physical properties of carboxylic acid Name Molecularformula Boiling point (°C) 101 118 141 164 Methanoic HCOOH acid(Formic acid) Ethanoic CH3COOH acid(Acetic acid) Propanoic acid Butanoic acid  C2H5COOH C3H7COH Solubility in water ± generally in carboxylic acid (the less than four carbon atoms) arevery soluble in water and ionise partially to form weak . Name of carboxylic acids Molecular formula of alcohol Methanoic acid(Formic HCOOH acid) Ethanoic acid(Acetic acid) Propanoic acid Butanoic acid CH3COOH C2H5COOH C3H7COH 4. General formula: CnH2n+1COOH  Where n = 0.    . ± COOH. Smell ± carboxylic acid (< 10 carbon) are colourless and pungent smell.Non-Hydrocarbon ± Carboxylic Acids 1. Carboxylic acids are non-hydrocarbons which contain carbon.

Reaction with metals Ethanoic acid reacts with reactive metals (copper and metals below it in the reactivity series cannot react with ethanoic acid).+ H+ Ethanoic acid turns moist blue litmus paper red. a colourless solution (magnesium ethanoate) is formed. butanol) CH3CO-OH + H-OC4H9 ±> CH3COOC4H9 + H2O (Concentrated H2SO4 is a catalyst) In this reaction. an ester (colourless sweet-smelling liquid) (butyl ethanoate) and water are formed. Na. a colourless solution (zinc ethanoate) is formed. a salt (sodium ethanoate) and water are formed. carbon dioxide and water are formed. Fe. Preparation of carboxylic acid  Oxidation of an alcohol The oxidation of ethanol is used to prepare ethanoic acid. Cu. Al. Pb. Reaction with carbonates Ethanoic acid reacts with metal carbonates (calcium carbonate. (K. propanol. 2CH3COOH + Mg ±> Mg(CH3COO)2 + H2 In this reaction. Zn. zinc carbonate). CH3COOH + NaOH ±> CH3COONa + H2O In this reaction. Reaction with bases acid neutralises alkalis (sodium hydroxide). Reaction with alcohols (Esterification) Ethanoic acid reacts with alcohol (ethanol. Mg. Hg. magnesium carbonate. 6. 2CH3COOH + CaCO3 ±> Ca(CH3COO)2 + CO2 + H2O In this reaction. CH3COOH <±> CH3COO. a salt (calcium ethanoate).5. Au) 2CH3COOH + Zn ±> Zn(CH3COO)2 + H2 In this reaction.     . Sn. Chemical properties of carboxylic acid  Acid properties Ethanoic acid is a weak monoprotic acid that ionises partially in water (produce a low concentration of hydrogen ions). C2H5OH + 2[O] ±> CH3COOH + H2O Carried out by refluxing* ethanol with an oxidising agent [acidified potassium dichromate(VI) solution ± orange colour turns to green / acidified potassium manganate(VII) solution ± purple colour turns to colourless] * reflux = upright Liebig condense to prevent the loss of a volatile liquid by vaporisation.

CnH2n+1COOH + CmH2m+1OH ±> CnH2n+1COOCmH2m+1 + H2O   First part: taken from the alcohol (alkyl group) Second part: taken from the carboxylic acid (-oic to -oate) Molecular formula of ester HCOOC2H5 CH3COOCH3 CH3COOC3H7 C2H5COOC2H5 Prepared from Name of ester Ethyl methanoate Methyl ethanoate Propyl ethanoate Ethyl propanoate Ethanol + Methanoic acid Methanol + Ethanoic acid Propanol + Ethanoic acid Ethanol + Propanoic acid . 2. Benzoic acid is used as food preservative. 3 « and m = 1. Esters are non-hydrocarbons which contain carbon. 2.7. The functional group in ester is carboxylate group. Butanoic acid is used to produce ester (artificial flavouring). 1.   Non-Hydrocarbon ± Esters 1. 2. General formula: CnH2n+1COOCmH2m+1 Where n = 0. 3 « (n and m = number of carbon) RCOORµ where R and Rµ represented the same or different alkyl groups. 3. Vinegar (dilute 4% of ethanoic acid) is used as preservative and flavouring. ± COO -. Uses of Carboxylic Acid    Carboxylic acid (methanoic acid and ethanoic acid) is used to coagulate latex. Ethanoic acid is used to make polyvinvyl acetate which is used to make plastics and emulsion paints. hydrogen and oxygen atoms.

Physical properties of ester Name 3-metylbutyl acetate Ethyl butanoate Octyl ethanoate Isoamyl isovalerate        Odour Banana Pineapple Orange Apple Simple esters are colourless liquid and are found in fruits and flowers. Waxes (beewax) are solid ester derived from long-chain fatty acids and long-chain alcohols. Esters have sweet pleasant smell.4. Esters are covalent compounds. Esters used as solvents for glue and varnishes. Natural sources:  Vegetable oils (palm oil) and liquids esters can be found in plants derived from glycerol and fatty acids. Esters are insoluble in water but soluble in organic solvent.   5. Esters are less dense than water. In plant. Esters are neutral and cannot conduct electricity. . Fats are solid esters (milk fat) derived from glycerol and fatty acids. Uses of Esters         Preparation of cosmetics and perfumes (esters are volatile and have sweet smell). Natural esters serves as storage reserve of energy in living things. Esters used to make plastics softer. wax (esters) helps to prevent dehydration and attack of microorganisms. The higher and more complex esters have higher boiling points and less volatile. Esters used to produce polyester (threads and synthetics fabrics) Esters used to produce soap and detergents. Synthetic esters used as food additives (artificial flavour).

Non-Hydrocarbon ± Fats 1. 6. 2. Physical properties of fats Saturated Types of fatty acids Bonding Melting point Sources Cholesterol State at room temperature C-C single bonds single higher animals high solid Unsaturated C=C double bonds double lower plants low liquid . Name of fat Molecular formula of ester Types of fatty acids Lauric acid* Palmitic acid* Stearic acid* Oleic oxide ** CH3(CH2)10COOH CH3(CH2)14COOH CH3(CH2)16COOH CH3(CH2)7CH=CH(CH2)7COOH Saturated Saturated Saturated Unsaturated Unsaturated Linoleic acid*** CH3(CH2)4CH=CHCH2CH=CH(CH2)7COOH Linolenic acid*** CH3CH2CH=CHCH2CH=CHCH2CH=CH(CH2)7COOH Unsaturated * Saturated: C-C single bonds ** Unsaturated (monounsaturated): C=C double bonds *** Unsaturated (polyunsaturated): C=C double bonds 4. Plant oils have higher percentage of unsaturated fatty acids than saturated fatty acids. Natural esters are formed from glycerol and fatty acids. Animal fats have higher percentage of saturated fatty acids than unsaturated fatty acids. hydrogen and oxygen atoms. Fatrs are non-hydrocarbons which contain carbon. 5. 3. Fats (lipids / triglycerides) are belonging to the group in ester.

Effect of fats Fatty food produce high energy but high consumption of fatty food will results:    obesity raise the level of cholesterol deposition will cause block the flow of blood which lead to stroke and heart attack. Chemical properties of fats  Unsaturated fats can be converted into saturated fats by hydrogenation (additional reaction) in 200°C and 4 atm in the presence of nickel catalyst. purification the oil (palm oil is treated with phosphoric acid and then steam is passed through to separate the acid) 7. palm oil and bran oil 7. peanut oil. vacuum . Example: olive oil.  8. digestion (crushing the husk and fruit and separate the oil by heating) 4. D.Fats (animal) in general are solids at room temperature and acted as:        thermal insulator protective cushion to protect the vital organ provide energy and stored in body carry Vitamin A. sterilising (oil palm fruit) 2. squeezed out the oil 5. K (insoluble in water) Example: butter. Example: production of margarine from sunflower oil of palm oil. fish oil (liquid in room temperature) Fats (plant) are called oils. Palm oil   It is extracted from fresh oil palm fruits. extraction (separate the oil from water) 6. 9. Palm oil ± extracted from the pulp of the fruits. Steps in extraction of palm oil: 1. E. Oils are liquids at room temperature. stripping 3.

rich in vitamin A (carotenoid) rich in vitamin E (tocophenols and tocotrienols) resist oxidation in high temperature. crushing the husk and fruit 4. Monomer: glucose (C6H12H6) Reaction to form polymer: condensation reaction (. cellulose. Polymer can be classified into two groups:  synthetic polymers / man-made polymers (polythene. easy to digest and absorb. Polymers 1. 2. artificial silk. starch. Natural polymer: Carbohydrates (polysaccharides) (starch.Palm kernel oil ± extracted from the kernel or seed. PVC ± polyvinyl chloride. extracting kernel oil 5. stripping 3. Steps in extraction of palm oil: 1. glycogen and cellulose)     General formula: Cx(H2O)y with the ratio of H:O = 2:1 Carbohydrates have cyclic structure. sterilising (oil palm fruit) 2. and proteins)  3. and polypropene) natural polymers (natural rubber. Polymer ± many small units (monomers) joining together to formed large molecule.H2O) . purification (purify the oil from kernel) Goodness in palm oil:      higher proportion of unsaturated fats.

Natural coagulation process of latex For the natural coagulation of latex: 1.H2O)    5. Monomer: isoprene.4. This prevent rubber from coagulate. A molecule of rubber contains 5000 isoprene units. The rubber molecules will collide after the protein membrane is broken. Coagulation process occurs in slower pace due to the bacteria (microorganism) action which produce acid) . 3. Natural polymer: Protein (polypeptide)  Protein consists of carbon. C3H8 or 2-methylbuta-1. suphuric acid and hydrochloric acid. Reaction to form polymer: additional polymerisation (one of the double bond in isoprene becomes single bond) 6. Structure of rubber molecule   Latex is colloid (35% rubber particles and 65% water). Rubber molecules (polymers) are set free 4. methanoic acid. phosphorus and other elements) Monomer: amino acids Amino acids have two functional group which are carboxyl group (-COOH) and amino group(NH2) Reaction to form polymer: condensation reaction (. Coagulation process of latex The process for the coagulation of latex is summarised as: 1.3-diene. 7. 2. 2. Example of acid: formic acid. Acid (H+) can neutralise the negatively-charged protein membrane. Latex is exposed to air without adding acid (duration ± overnight). oxygen and nitrogen (some have sulphur. hydrogen. Rubber molecules combine with one another (coagulation). Natural polymer: Natural rubber     Extracted from the latex of rubber tree (Hevea brasiliensis) which the tree originates from Brazil. Same charge of rubber molecules repels each other. Rubber particle contains rubber molecules which are wrapped by a layer of negatively-charged protein membrane. 8.

This also reduces the number of carbon-carbon double bonds in rubber molecules. sunlight and other chemicals. Positively-charged hydrogen ion / H+ produced by bacteria can be neutralised by negativelycharged hydroxide ion / OH. 10. hard and brittle ± cooled) easily oxidised (present of C=C) insoluble in water (due to the long hydrocarbon chains) soluble in organic solvent (propanone. decompose ± above 200°C.9. ozone. This increases the molecular size and the intermolecular forces of attraction between rubber molecules. 12. vulcanised rubber is more resistant to heat (does not become soft and sticky when hot). vulcanised rubber is more elastics and stronger. Prevent coagulation process of latex The following are latex coagulation prevention method: 1. Vulcanisation of rubber Vulcanisation ± process of hardening rubber and increases rubber elasticity by heating it withsulphur or sulphur compounds.)    11. Methods:   heating natural rubber with sulphur at 140°C using zinc oxide as catalyst or dipping natural rubber in a solution of disulphur dichloride (S2Cl2) in methylbenzene. Therefore.   . benzene. Therefore. 2. Properties of vulcanisation of rubber  The sulphur atoms are added to double bonds in the natural rubber molecules to formdisulphide linkages (-C-S-S-C-) / sulphur cross-links between the long polymer chains. vulcanised rubber is more resistant to oxygen. Therefore.from ammonia solution. petrol etc. Properties of natural rubber   elastic cannot withstand heat (become sticky and soft ± above 50°C. Example: ammonia (NH3). Alkaline / Basic solution is added to the latex.

13. Strong and hard (depends on degree of vulcanisation) Low Less elastics Strength and hardness Weak and soft (polymer chain of rubber will break when rubber is over stretched. Comparison between the properties of vulcanised rubber and unvulcanised rubber Properties Double bonds Melting point Elasticity Vulcanised rubber Unvulcanised rubber Decreases (formation of sulphur More number of double cross-links) bonds High (presence of sulphur) More elastic (sulphur crosslinks prevents the polymer chain or rubber from slipping past. R & D of rubber     RRIM ± Rubber Research Institute of Malaysia MRB ± Malaysian Rubber Board Rubber Technology Centre Various local higher institutions of learning . Poor resistant to heat Resistant to heat Resistant to heat Oxidation Resistant to oxidation Easily oxidised by oxygen. . (reduction of number of double UV light (presence of many bonds per rubber molecule) double bonds per rubber molecules) 14.

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