Draw the skeletal structure of the products formed when the given triacylglycerol is hydrolyzed with water in the presence of sulfuric acid. You may draw the structures in any arrangement that you like, so long as they aren't touching. Im +

Indicate which of the terms monosaccharide, disaccharide, reducing sugar, anomers, enantiomers, and aldohexose applies to both members of each of the following pairs of substances. More than one term may apply to a given pair of substances. a-D-Glucose and a-D-galactose- Sucrose and cellobiose- Glyceraldehyde and dihydroxyacetone- D-Ribose and L-ribose-

Mild hydrolysis of a glycolipid produces an L-glucose molecule and the salt of tetra-decanoate fatty acid. Draw the structure of the glycolipid.

An unknown trisaccharide was treated with dimethyl sulfate which adds a methyl group to every free OH group. It was then subjected to acid hydrolysis (to break glycoside bonds). The products were 23, 4, 6-tetra-O-methylgalactosc, 23,4-ui-O methyl glucose, and 2,3.6-tri-O methylglucose. Treatment of the intact trisaccharide with 0(1 6)-gaiactosidase yielded galactose and a saccharide. Treatment of this disaccharide with a(l 4)-glucosidase yielded D glucose. Draw the structure of this trisaccharide and give its systematic name.