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1 18.3Waxes, Fats, and Oils 18.4Chemical Properties of Triacylglycerols Chapter 18 Lipids.

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Presentation on theme: "1 18.3Waxes, Fats, and Oils 18.4Chemical Properties of Triacylglycerols Chapter 18 Lipids."— Presentation transcript:

1 1 18.3Waxes, Fats, and Oils 18.4Chemical Properties of Triacylglycerols Chapter 18 Lipids

2 2 Waxes Waxes are: Esters of saturated fatty acids and long- chain alcohols. Coatings that prevent loss of water by leaves of plants.

3 3 In a triacylglycerol, glycerol forms ester bonds with three fatty acids. Triacylglycerols

4 4 Olestra, A Fat Substitute Olestra is: Used in foods as an artificial fat. Sucrose linked by ester bonds to several long- chain fatty chains. Not broken down in the intestinal tract.

5 5 The chemical reactions of triacylglycerols are similar to those of alkenes and esters. In hydrogenation, double bonds in unsaturated fatty acids react with H 2 in the presences of Ni or Pt catalyst. In hydrolysis, ester bonds are split by water in the presence of an acid, a base, or an enzyme. Chemical Properties of Triacylglycerols

6 6 Hydrogenation of Oils Hydrogenation: Adds hydrogen to double bonds in oils to form single bonds. Produces solid shortening, margarine, and other products.

7 7 Hydrogenation Hydrogenation converts double bonds to single bonds.

8 8 In hydrolysis, triacylglycerols are split into glycerol and three fatty acids. An acid or enzyme catalyst is required. Hydrolysis

9 9 Soaps are: Salts of fatty acids. Formed by saponification, a reaction in which a triacylglycerol reacts with a strong base. Saponification and Soap


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