Structure of Fats and Oils Simplified Revision Notes for Scottish Highers Chemistry
Revision notes with simplified explanations to understand Structure of Fats and Oils quickly and effectively.
Learn about Fats and Oils for your Scottish Highers Chemistry Exam. This Revision Note includes a summary of Fats and Oils for easy recall in your Chemistry exam
253+ students studying
Fats and Oils Quizzes
Test your knowledge with quizzes.
Fats and Oils Flashcards
Practice with bite-sized questions.
Fats and Oils Questions by Topic
Prepare with real exam question.
Structure of Fats and Oils
Formation of Fats and Oils
Fats and oils are esters formed when glycerol (propane-1,2,3-triol), a trihydric alcohol with three hydroxyl groups, condenses with carboxylic acids, known as fatty acids.
The reaction between glycerol and three fatty acids results in the formation of fats and oils.
Composition of Fats and Oils
Each molecule of glycerol condenses with three molecules of fatty acid.
Hydrolysis of fats and oils yields fatty acids and glycerol in the ratio of three moles of fatty acid to one mole of glycerol.
Nature of Fats and Oils
All fats and oils are naturally occurring esters produced through condensation reactions between glycerol and various long-chain carboxylic acids known as fatty acids.
Glycerol is also referred to as propane-1,2,3-triol and has three hydroxyl functional groups.
Fatty acids are long-chain carboxylic acids with carbon chain lengths ranging from C₄ to C₂₆.
Common fatty acids like stearic acid and oleic acid typically have eighteen carbon atoms in their chains.
Fats and oils formed through these reactions are known as triglycerides.
Structural Formula of Triglycerides
The structural formula of a fat or oil (a triglyceride) consists of three fatty acid chains joined to a glycerol molecule.
The fatty acid chains are attached to glycerol through ester linkages.
Fats and oils are esters like other ester compounds.
Distinguishing Fats from Oils
Oils are liquids at room temperature, while fats are solids at room temperature.
Oils contain a higher number of carbon-to-carbon double bonds (unsaturated bonds) compared to fats.
Structure of Fats and Oils
Melting Points of Fats and Oils
Oils have lower melting points due to their higher degree of unsaturation and the resulting distortion in their molecular shape.
The weaker London dispersion forces between oil molecules result from their poorer packing.
Fats, on the other hand, have less distortion and can pack closely together, leading to higher melting points.
Hardening of Oils
To increase the melting point of an oil, additional reactions can occur between the double bonds and hydrogen, reducing unsaturation and causing hardening.
This process involves converting unsaturated fats into saturated fats.
Testing for Unsaturation: Bromine Test
The bromine test can be used to determine the level of unsaturation in a fat or oil.
Bromine solution decolorises quickly when it reacts with unsaturated compounds.
The more double bonds present in the fat or oil, the more bromine solution can be decolourised.
Conclusion:
Fats and oils are esters formed by condensation reactions between glycerol and fatty acids.
Their properties, such as melting points, are influenced by the degree of saturation (presence of double bonds) in the fatty acid chains.
Unsaturated oils have lower melting points due to weaker intermolecular forces, while saturated fats have higher melting points.
The bromine test is a useful method for assessing the level of unsaturation in fats and oils.
Only available for registered users.
Sign up now to view the full note, or log in if you already have an account!
500K+ Students Use These Powerful Tools to Master Structure of Fats and Oils For their Scottish Highers Exams.
Enhance your understanding with flashcards, quizzes, and exams—designed to help you grasp key concepts, reinforce learning, and master any topic with confidence!