Alcohols and Hydrogen bonding Simplified Revision Notes for Scottish Highers Chemistry
Revision notes with simplified explanations to understand Alcohols and Hydrogen bonding quickly and effectively.
Learn about alcohols for your Scottish Highers Chemistry Exam. This Revision Note includes a summary of alcohols for easy recall in your Chemistry exam
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Alcohols and Hydrogen bonding
Alcohol Polarity and Hydrogen Bonding
Alcohols, represented as R-OH, have a hydroxyl (-OH) group, making them polar molecules.
The electronegative oxygen atom in the hydroxyl group (O-H) contributes to their polarity.
Hydrogen Bonding and Boiling Points
Hydrogen bonding occurs between alcohol molecules due to the presence of the -OH group.
This bonding leads to higher boiling points for alcohols compared to alkane molecules with similar molecular masses.
Example: Boiling Points
Methanol (CH3OH, mass = 32) has a boiling point of 64.7 °C.
Ethane (C2H6, mass = 30) has a significantly lower boiling point of -88.6 °C.
Alcohol's Compatibility with Water:
Alcohols can mix with water because their hydroxyl (-OH) groups can form hydrogen bonds with water molecules.
Conclusion
Alcohols, with their hydroxyl groups, exhibit polarity and the ability to engage in hydrogen bonding.
Hydrogen bonding contributes to the higher boiling points of alcohols compared to non-polar compounds.
This ability to form hydrogen bonds allows alcohol to mix readily with water.
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