Exam 28: Carbohydrates

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Which of the following sugars can be classified as a ketohexose? Which of the following sugars can be classified as a ketohexose?

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Upon hydrolysis of cellulose, what sugar is formed?

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What are the products of the following reaction? What are the products of the following reaction?

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Which of the following pairs of carbohydrates will afford the same product from a Wohl degradation?

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What is the correct chair form for the banomer of D-glucose? What is the correct chair form for the banomer of D-glucose?

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Which of the following sugars can be classified as a ketotetrose? Which of the following sugars can be classified as a ketotetrose?

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Which is the correct Haworth projection for the aanomer of allose? Which is the correct Haworth projection for the aanomer of allose?

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How many possible stereoisomers are there of the following heptose? How many possible stereoisomers are there of the following heptose?

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Upon hydrolysis of amylopectin, what sugar is formed?

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Upon hydrolysis of amylose, what sugar is formed?

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What is the composition of lactose?

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What is the composition of sucrose?

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Does a monosaccharide prefer to exist in the open-chain or closed-ring form?

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Which of the following sugars can be classified as an aldohexose? Which of the following sugars can be classified as an aldohexose?

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What is the composition of maltose?

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After a series of Kiliani-Fischer syntheses on D-glyceraldehyde, an unknown sugar was isolated from the reaction mixture.The following experimental data was obtained.What is the structure of this unknown sugar? Data: - Molecular formula: C6H12O6 - Reacts with phenylhydrazine to give an osazone, mp 178°C.- Reacts with HNO3 to give an optically active aldaric acid.- Wohl degradation followed by HNO3 oxidation gives an optically inactive Aldaric acid.- Two Wohl degradations followed by HNO3 oxidation give a meso-tartaric acid. <sup> </sup>After a series of Kiliani-Fischer syntheses on D-glyceraldehyde, an unknown sugar was isolated from the reaction mixture.The following experimental data was obtained.What is the structure of this unknown sugar? Data: - Molecular formula: C<sub>6</sub>H<sub>12</sub>O<sub>6</sub> - Reacts with phenylhydrazine to give an osazone, mp 178°C.- Reacts with HNO<sub>3</sub> to give an optically active aldaric acid.- Wohl degradation followed by HNO<sub>3</sub> oxidation gives an optically inactive Aldaric acid.- Two Wohl degradations followed by HNO<sub>3</sub> oxidation give a meso-tartaric acid.

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The following reaction is an example of a base-catalyzed epimerization reaction in which a ketose is converted to a pair of aldoses.What are the products from this reaction? <sup> </sup>The following reaction is an example of a base-catalyzed epimerization reaction in which a ketose is converted to a pair of aldoses.What are the products from this reaction?

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From the sugars shown below, which one is a non-reducing sugar? From the sugars shown below, which one is a non-reducing sugar?

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