Asparagusic Acid vs Allyl isothiocyanate Simplified Revision Notes for Scottish Highers Chemistry
Revision notes with simplified explanations to understand Asparagusic Acid vs Allyl isothiocyanate quickly and effectively.
Learn about Chemistry of Cooking for your Scottish Highers Chemistry Exam. This Revision Note includes a summary of Chemistry of Cooking for easy recall in your Chemistry exam
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Asparagusic Acid vs Allyl isothiocyanate
Asparagusic Acid vs Allyl isothiocyanate
Asparagusic Acid:
Contains a carboxyl group (COOH) with an O-H bond.
This functional group allows it to form hydrogen bonds with water molecules.
Allyl Isothiocyanate:
Contains non-polar bonds.
As a result, it cannot form hydrogen bonds with water molecules.
Cooking Methods:
Asparagus (Containing Asparagusic Acid):
Since asparagusic acid can form hydrogen bonds with water, it is better suited for cooking in water.
When asparagus is cooked in water, the polar asparagusic acid molecules dissolve in the water and are lost when the water is drained away.
Broccoli (Containing Allyl Isothiocyanate):
Allyl isothiocyanate, being non-polar, does not interact well with water.
Therefore, broccoli, which contains allyl isothiocyanate, should be cooked in a nonpolar cooking medium like oil.
When broccoli is cooked in oil, the non-polar allyl isothiocyanate molecules dissolve in the oil and are lost from the broccoli.
Considerations:
The choice of cooking method for these vegetables ensures that the flavour compounds are retained within the food.
However, there may be some trade-offs. For example, cooking asparagus in water may cause the loss of polar molecules like Vitamin C, which dissolve in water.
Summary:
Asparagusic acid (found in asparagus) is better preserved when cooked in water due to its ability to form hydrogen bonds with water molecules.
Allyl isothiocyanate (found in broccoli) is better retained when cooked in oil because it cannot form hydrogen bonds with water molecules.
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