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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

What functional groups are found in all monosaccharides?

Sophorose, a carbohydrate found in certain types of beans, has the following Haworth structure:

a. Is sophorose a mono-, di-, or polysaccharide?

b. What are the monosaccharides in sophorose?

c. What is the glycosidic link in sophorose?

d. Is this the 伪or 尾isomer of sophorose?

e. Is sophorose a reducing sugar?

Draw the Fischer projection for the other enantiomer of a to d in problem 13.21.

Identify the chiral carbon if any in each of the following compounds

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)
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