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Chapter 13: Q. 13.26 (page 446)

Draw the Fischer projections for D-fructose and L-fructose.

Short Answer

Expert verified

D-Fructose and L-Fructose Fischer projections-

Step by step solution

01

Given Information

We have to draw the fisher projection of D-Fructose and L-Fructose

02

Explanation

In a D-isomer, the - OH bunch is available on the right half of the chiral carbon. In L-isomer, the -OH bunch is available towards the left of the chiral carbon in the Fischer projection. In the event that a compound has more than one chiral carbon, the isomer is assigned as L or D, contingent upon the place of the - OH bunch present chiral carbon farthest from the carbonyl carbon.

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Most popular questions from this chapter

For each of the following, give the monosaccharide units produced by hydrolysis, the type of glycosidic bond, and the name of the disaccharide including 伪or 尾:

Indicate whether each disaccharide in the following figure is a reducing sugar or not.

a.

b.

伪-Cellobiose is a disaccharide obtained from the hydrolysis of cellulose. It is quite similar to maltose except it has a 尾(1鈫�4)-glycosidic bond. Draw the Haworth structure for伪-cellobiose. (13.4, 13.6)

Identify the disaccharide that fits each of the following descriptions:

a. not a reducing sugar

b. composed of two glucose units

c. also called milk sugar

d. hydrolysis gives glucose and fructose

Raffinose, found in Australian manna and in cottonseed meal, has the following Haworth structure:

(13.4,13.5,13.6)

a. Is raffinose a mono-, di-, or trisaccharide?

b. What monosaccharides are present in raffinose?

c. Is raffinose a reducing sugar?
See all solutions

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