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Summary Alcohols and Haloalkanes

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Contains all parts of the Chemistry A OCR specification for alcohols and haloalkanes

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Topic 4.3 Alcohols and Haloalkanes Notes


Why do alcohols have higher boiling points than alkanes?

Alcohols have van der Waals’ forces and hydrogen bonding intermolecular forces. Hydroxyl groups in
alcohols allow hydrogen bonding to occur between alcohol molecules. Alkanes only have van der
Waals’ forces between molecules. This means that more energy is needed to overcome hydrogen
bonding in alcohols, so boiling point is higher in alcohols.



Why are alcohols soluble in water?

Alcohols form hydrogen bonds with water as the OH group is hydrophilic, and the OH group is
attracted to H2O molecules, enhancing solubility.



Classifying primary, secondary and tertiary alcohols

A primary alcohol is an alcohol whose OH group is attached to only one single alkyl group.

Eg.



A secondary alcohol is an alcohol whose OH group is attached to a saturated carbon atom which has
two other carbons attached to it.

Eg.



A tertiary alcohol is an alcohol whose OH group is attached to a saturated carbon which has three
other carbons attached to it.

Eg.




Equations for:

Complete combustion:

Methanol + oxygen  carbon dioxide + water

2CH3OH (l) + 3O2 (g)  2CO2 (g) + 4H2O (l)

Ethanol + oxygen  carbon dioxide + water

2C2H5OH (l) + 6O2 (g)  4CO2 (g) + 6H2O (l)

Propanol + oxygen  carbon dioxide + water

2C3H7OH (l) + 9O2 (g)  6CO2 (g) + 8H2O (l)

Butanol + oxygen  carbon dioxide + water

2C4H9OH (l) + 12O2 (g)  8CO2 (g) + 12H2O (l)

, Topic 4.3 Alcohols and Haloalkanes Notes


Incomplete combustion:

Methanol + oxygen  carbon monoxide + water

CH3OH + O2  CO + 2H2O

Ethanol + oxygen  carbon monoxide + water

C2H5OH + 2O2  2CO + 3H2O

Propanol + oxygen  carbon monoxide + water

C3H7OH + 3O2  3CO + 4H2O

Butanol + oxygen  carbon monoxide + water

C4H9OH + 4O2  4CO + 5H2O

Oxidation of alcohols:




Partial oxidation of primary alcohols:

Ethanol + oxygen  ethanal

C2H5OH + [O]  CH3CHO
Primary Aldehyde
alcohol

Complete oxidation of primary alcohols:

Ethanol + oxygen  ethanoic acid

C2H5OH + [O]  CH3COOH
Primary Carboxylic
alcohol acid

Partial oxidation of secondary alcohols:
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