Chapter 25: Problem 16
Define the term anomeric carbon. In glucose, which carbon is the anomeric carbon?
Chapter 25: Problem 16
Define the term anomeric carbon. In glucose, which carbon is the anomeric carbon?
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Get started for freeMannose exists in aqueous solution as a mixture of \(\alpha\)-D-mannopyranose and \(\beta\)-D-mannopyranose. Draw Haworth projections for these molecules.
Which carbon of an aldopentose determines whether the pentose has a D or L configuration?
An important technique for establishing relative configurations among isomeric aldoses and ketoses is to convert both terminal carbon atoms to the same functional group. This can be done either by selective oxidation or reduction. As a specific example, nitric acid oxidation of D-erythrose gives meso- tartaric acid (Section 3.4B). Similar oxidation of D-threose gives \((2 S, 3 S)\)-tartaric acid. Given this information and the fact that D-erythrose and D-threose are diastereomers, draw Fischer projections for D-erythrose and D-threose. Check your answers against Table 25.1.
Following is a chair conformation for the repeating disaccharide unit in chondroitin 6-sulfate. This biopolymer acts as the flexible connecting matrix between the tough protein filaments in cartilage. It is available as a dietary supplement, often combined with D-glucosamine sulfate. Some believe this combination can strengthen and improve joint flexibility. (a) From which two monosaccharide units is the repeating disaccharide unit of chondroitin 6-sulfate derived? (b) Describe the glycosidic bond between the two units.
Draw a structural formula for the \(\beta\) - \(N\)-glycoside formed between 2 -deoxyD-ribofuranose and adenine.
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