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Chapter 28: Question 28.39 (page 1147)

Classify each compound as identical to A or its enantiomer.

(a.)

(b.)

(c.)

Short Answer

Expert verified

Answer

  1. Identical.
  2. Identical.
  3. Enantiomer.

Step by step solution

01

Enantiomers and Identical isomers.

Enantiomers are the mirror image compounds which are having opposite configuration to the given compound; this means they are non-superimposable.

Identical isomers are those which have same arrangements and have same configuration.

02

Compounds which are identical to A.

The a and b parts are having same R configuration as that of A. So, these compounds are identical.

Compounds those are identical to A.

03

Compounds which are enantiomer of A.

The c part is having S configuration whereas A has R configuration. So, this compound is enantiomer of A.

Compounds that are enantiomer of A

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Most popular questions from this chapter

Draw the products formed when α-D-glucoseis treated with each reagent.

a.CH3I,Ag2O

b.CH3OH,HCl

c. Ac2O, pyridine

d. The product in (a), thenH3O+

e. The product in (b), then Ac2O, pyridine

f. The product in (d), then C6H5CH2Cl,Ag2O

Which aldoses are oxidized to optically inactive aldaric acids: (a) D-erythrose; (b) D-lyxose; (c) D-galactose?

Convert each compound to a Fischer projection and label each stereogenic center as R or S.

(a.)

(b.)

(c.)

(d.)

(e.)

(f.)

a. Identify the glycosidic linkage in disaccharide C, classify the glycosidic bond as αorβ, and use numbers to designate its location.

b. Identify the lettered compounds in the following reaction.

As we have seen in Chapter 28, monosaccharides can be drawn in a variety of ways, and in truth, often a mixture of cyclic compounds is present in a solution. Identify each monosaccharide, including its proper D, L designation, draw in a less-than-typical fashion.

(a.)

(b.)

(c.)

(d.)
See all solutions

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