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Lecture on Alkanes
Jul 20, 2024
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Lecture on Alkanes
Introduction to Alkanes
Also called paraffins or harafins
Saturated hydrocarbons: Each carbon in alkanes is SP3 hybridized.
General molecular formula: $C_nH_{2n+2}$
Simplest member: Methane ($CH_4$)
Examples and Structural Formulas
Methane: $CH_4$
Ethane: $C_2H_6$
Propane, Butane, etc.
Structural representations: Using strokes for showing bonds.
Naming Compounds
Example 1: 9-carbon chain
Longest continuous chain: 9 carbons ($C_9$)
Named “nonane” (Single-bonded/n-alkane)
Substituents: Methyl and ethyl groups considered
Example name: 4-ethyl-5-methyl-nonane
Example 2: Compound with bromine ($Br$)
Preparation of Alkanes
1. Hydrogenation of Alkenes
Addition of hydrogen ($H_2$) to alkenes
Catalysts: Platinum (Pt), Palladium (Pd), Nickel (Ni)
Example: Propene ($C_3H_6$) + Hydrogen -> Propane ($C_3H_8$)
2. Reduction of Alkyl Halides
Halogen substituted with hydrogen
Methods:
Hydrolysis of Grignard Reagents ($RMgX$): Important for exams
Reduction by Metal and Acid (e.g., Zinc and Hydrochloric Acid)
Physical Properties of Alkanes
State of matter:
First four (C1 to C4) are gases.
Next thirteen (C5 to C17) are liquids.
18 carbons and above are solids.
Solubility:
Soluble in non-polar solvents like benzene.
Insoluble in water.
Reactions of Alkanes
1. Halogenation
Example: Methane ($CH_4$) + Chlorine ($Cl_2$) -> Chloromethane ($CH_3Cl$) + Hydrogen Chloride ($HCl$)
Further chlorination results in di-, tri-, and tetra-chloromethane.
Most reactive: Fluorine, Chlorine, Bromine.
Iodine does not react.
2. Combustion
Burning in the presence of oxygen.
General formula: $C_nH_{2n+2} + (3n+1)/2 O_2 -> n CO_2 + (n+1) H_2O$
Example: Methane combustion yields Carbon Dioxide ($CO_2$) and Water ($H_2O$).
3. Pyrolysis (Cracking)
Decomposition by heat (600°C)
Large alkanes break into smaller alkanes and alkenes.
Example: Pentane ($C_5H_{12}$) -> Smaller alkane ($C_2H_6$) + Alkene ($C_3H_6$)
Conclusion
Summary of alkanes and their reactions.
Future lectures will cover Alkenes and Alkynes.
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