Chapter 28: Question 28.54 (page 1149)
What products are formed when each compound is subjected to a Kiliani–Fischer synthesis?
(a.)
(b.)
Short Answer
Answer
(a.)
(b.)
Chapter 28: Question 28.54 (page 1149)
What products are formed when each compound is subjected to a Kiliani–Fischer synthesis?
(a.)
(b.)
Answer
(a.)
(b.)
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Get started for freeClassify each compound as identical to A or its enantiomer.
(a.)
(b.)
(c.)
Consider the tetrasaccharide stachyose drawn below. Stachyose is found in white jasmine, soybeans, and lentils. Because humans cannot digest it, its consumption causes flatulence.
a. Label all glycoside bonds.
c. What products are formed when stachyose is hydrolyzed with H3O+?
d. Is stachyose a reducing sugar?
e. What product is formed when stachyose is treated with excess CH3I, Ag2O?
f. What products are formed when the product in (e) is treated with H3O+?
Treating chitin with hydrolyzes its amide linkages, forming a compound called chitosan. What is the structure of chitosan? Chitosan has been used in shampoos, fibers for sutures, and wound dressings.
Draw the structure of a disaccharide formed from two mannose units joined by a glycosidic linkage.
Convert each compound to a Fischer projection and label each stereogenic center as R or S.
(a.)
(b.)
(c.)
(d.)
(e.)
(f.)
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