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Sources of Hydrocarbons
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Hydrocarbons Hydrocarbons are compounds consisting of hydrogen and carbon only, bonded together covalently.
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Sources Fossil Fuels Crude Oil Natural gas Coal
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Crude oil and natural gas were formed from the remains of marine plants and animals.
Coal was produced from dead wood
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Hydrocarbons CH4 Methane
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Methane Production Methane can be produced in: Coalmines Slurry pits
Waste dumps Digestive tracts of animals
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Hazards of Methane Production
Fires and explosions Death by suffocation Contributes to the greenhouse effect
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When the chain is between 5 and 9 carbons, the hydrocarbon is gasoline
When the chain is between 5 and 9 carbons, the hydrocarbon is gasoline. About a dozen carbons and it is diesel. Around 20 carbons is motor oil. A chain of hundreds to thousands of carbon and hydrogens make plastic. This particular plastic is polyethylene.
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Petroleum distillation
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Carbon groups Alkanes CnH2n+2 Methane CH4 GAS Ethane C2H6 GAS
Propane C3H GAS Butane C4H GAS Pentane C5H LIQUID Hexane C6H LIQUID
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Naming carbon groups Methyl CH3 Ethyl C2H5 Propyl C3H7 Butyl C4H9
Pentyl C5H11
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Alkanes Hydrocarbon chains where all the bonds between carbons are SINGLE bonds Name uses the ending –ane Examples: Methane, Propane, Butane, Octane, 2-methylpentane
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Step 1. Find the parent chain.
Where is the longest continuous chain of carbons?
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Step 2. Number the parent chain.
Number the parent chain so that the attached groups are on the lowest numbers Methyl is on carbon #2 of the parent chain Methyl is on carbon #4 of the parent chain GREEN is the right way for this one! 2 7 1 Groups on 2 and 5 Groups on 4, 6, and 7 Groups on 2, 3, and 5 Groups on 3 and 6
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Step 3. Name the attached groups.
Carbon (alkyl) groups Methyl CH3 - Ethyl CH3CH2- Propyl CH3CH2CH2 – Halogens Fluoro (F-) Chloro (Cl-) Bromo (Br-) Iodo (I-)
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Step 4. Designate where the group is attached to the parent chain.
Use the numbers of the parent chain from step 2 to designate the location of the attached groups to the parent chain. 2-methyl
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Step 5. Alphabetize the groups, combine like groups, and assemble.
The prefixes di, tri, tetra etc., used to designate several groups of the same kind Prefixes are not considered when alphabetizing (Example: dimethyl = m for alphabetizing) Parent chain goes LAST 1,1,1-trichloro-1-fluoromethane 1,1-dichloro-1,1-difluoromethane
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Draw Some Simple Alkanes
2-methylpentane 3-ethylhexane 2,2-dimethylbutane 2,3-dimethylbutane
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Alkenes CnH2n-2 Ethene Propene Butene Pentene Hexene
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Alkenes
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Preparation and properties of Ethene gas
Aluminium oxide(CATALYST) removes a water molecule from ethanol and produces ethene gas
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Preparation of ethene
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Practical precautions of ethene
Avoid suck back by removing heat before dismantling the equipment Discard first gas jar as it will have a mix of air and ethene
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Precautions Why is it desirable to push the glass wool into the tube after the ethanol has been added? To ensure that all of the ethanol is soaked up. Why should the ethanol not be heated strongly? Strong heating of the ethanol will cause it to evaporate too quickly and escape from the tube before it can be dehydrated.
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Combustion C₂h₄ + 3O₂ → 2CO₂ + 2H₂o Lime water test
PHYSICAL PROPERTIES: It is a colourless gas with a sweetish smell. It is insoluble in water so you can collect it over water. Combustion C₂h₄ + 3O₂ → 2CO₂ + 2H₂o Lime water test
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Ethyne preparation
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Preparation of ethyne The first test tube should be discarded.
Add small amounts of calcium carbide as it is very reactive with water
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TOLLENS REAGENT TEST FOR ALDEHYDES
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Aldehydes and ketones behave differently.
You will remember that the difference between an aldehyde and a ketone is the presence of a hydrogen atom attached to the carbon-oxygen double bond in the aldehyde. Ketones don't have that hydrogen. Fehlings test is used to distinguish the diffference in functional groups.
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