Exam 20: The Organic Chemistry of Carbohydrates

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Which of the following corresponds to the definition of an aldopentose? I.It is a monosaccharide. II)It contains a CHO group III)It is a disaccharide. IV)It is an oligosaccharide.

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Cell-surface carbohydrates play an important role in

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Provide the structure of the more stable chair conformer which results when β-D-galactose is treated with excess acetic anhydride/pyridine.

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Give the major product(s)for the following reaction.You may choose more than one answer. Give the major product(s)for the following reaction.You may choose more than one answer.

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Which of the following would give a positive Tollen's test?

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When D-sorbose (shown below)is treated with NaBH4,which of the following is produced? When D-sorbose (shown below)is treated with NaBH<sub>4</sub>,which of the following is produced?

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When pure α-D-glucopyranose is dissolved in water,the optical rotation of the resulting solution changes over a period of time.What is the name of this phenomenon and why does it occur?

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Given the structure of D-altrose below,provide the Haworth structure of β-D-altropyranose. Given the structure of D-altrose below,provide the Haworth structure of β-D-altropyranose.

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Which of the following statements best describes the meaning of a glycoside?

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Give the major product(s)for the following reaction. Give the major product(s)for the following reaction.

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When D-tagatose is added to a basic aqueous solution,an equilibrium mixture of three monosaccharides is obtained.Identify the monosaccharides. When D-tagatose is added to a basic aqueous solution,an equilibrium mixture of three monosaccharides is obtained.Identify the monosaccharides.

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Give the major product(s)for the following reaction. Give the major product(s)for the following reaction.

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Which monosaccharides are formed in the Kiliani-Fischer synthesis starting with D-xylose? Which monosaccharides are formed in the Kiliani-Fischer synthesis starting with D-xylose?

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How many chirality centers are there in an aldohexose?

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Epimers are essentially

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Give the product(s)for each step of the following reaction. Give the product(s)for each step of the following reaction.

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Which of the following compounds is a D-sugar?

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At which carbon are the following sugars epimers of each other? At which carbon are the following sugars epimers of each other?

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Two D-aldopentoses give the same D-aldotetrose upon Ruff degradation.The two aldopentoses are

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Provide the structure of the product which results when D-ribose is treated with bromine water.

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