Fischer projection.
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- Consider the following blood group A, B, AB and O.What are the sugar(carbohydrate ) content of their glycolipid?what are the formal chemical names for sucrose,lactose and maltose? ex. celllubiose is B-D-Glucopyranosyl1-(1->4)-B-D-glucopyranose. how do you get the answer?Which of an alpha-D-2,3-di-O-methylglucopyranose or alpha-D-2,3, 6-tri-O-methylglucopyranose represents a glucose unit in glycogen which was originally carrying an (alpha 1-->6) glycosidic bond?
- Indicate whether the following pairs of monosaccharides are aldoses or ketoses. a. D-altrose & D-xylose b. D-arabinose & D-glyceraldehyde c. D-erythrulose & D-psicose d. D-talose & D-gulose e. dihydroxyacetone & D-tagatose f. D-idose & D-threoseMatch the following structural composition with the corresponding polysaccharide Linear homoglycan of glucose connected by α1-4 linkages Branched glycan formed by alternating units of D-galactose and L-galactose Linear sulfated chains of alternating β-D-galactopyranose and 3,6-anhydro- α-galactopyranosyl units Poly-β-Dmannopyranosyluronic acid and/or Poly-α-L-gulopyranosyluronic acid Repeating Poly-D-galacturonic acid residues…Indicate whether each of the following pairs of sugars consists of anomers , epimers , or an aldose–ketose pair: (a) D - glyceraldehyde and dihydroxyacetone (b) D -glucose and D -mannose (c) D -glucose and D -fructose (d) α - D -glucose and β - D -glucose (e) D -ribose and D - ribulose (f) D - galactose and D -glucose
- What is the correct systematic name for the disaccharide below? Question 6 options: a O-β-D-glucopyranosyl-(1-->2)-α-D-glucopyranose b O-β-D-glucopyranosyl-(1-->4)-β-D-glucopyranose c O-α-D-glucopyranosyl-(1--> 2)-α-D-glucopyranose d O-β-D-glucofuranosyl-(1--> 4)-β-D-glucofuranoseAn 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.The following structure is sorbose Answer the following questions and briefly explain Draw β-D-sorbufuranose Draw β-D-sorbufuranosyl(2->1) β-D-glucopyranoside. Is this reducing sugar? What would be the probable function of this disaccharide, structural or storage?
- Complete the following table by providing the Fischer and Haworth Projections of the given sugars. (Please be careful with the alpha and beta, and the complete and abbreviated) (not a graded question) Sugar Fischer Projection Haworth Projection (Complete) alpha-anomer Haworth Projection (Abbreviated) beta-anomer L-Galactose L-FructoseRaffinose, the most abundant trisaccharide found in nature, occurs in whole grains and numerous vegetables (e.g., asparagus, cabbage, and beans). Hydrolysis of raffinose yields galactose and sucrose. Provide the systematic name for this trisaccharide. Is raffinose a reducing or nonreducing sugar? Is raffinose capable of mutarotation?In order to metabolize lactose, most infants express the enzyme lactase in their intestines. What kind of glycosidic linkage does lactose have? Please draw the individual monosaccharides to explain your answer. Please explain how the monosaccharides in lactose will be used in glycolysis. Be specific.