The structure on right side is of D-Idose. The enantiomer of D-Idose is L-Idose. This L-Idose is an epimer of D-Glucose at carbon no. 5. Another structure on left side is of Galactose which is an epimer of Glucose with difference on carbon number 4. So , these structures can be best described as epimers.
Why the answer is D? (I think the two epimers have opposite configuration at only "one"...
1) SHOW WORK STEP By STEP below is Figure 7-3 Recognizing Epimers Using Figure 7-3, identify the epimers of (a) D-allose, (b) D-gulose, and (c) D-ribose at C-2, C-3, and C-4. Answer Epimers differ by the configuration about only one carbon. (a) D-altrose (C-2), D-glucose (C-3), D-gulose (C-4) (b) D-idose (C-2), D-galactose (C-3), D-allose (C-4) (c) D-arabinose (C-2), D-xylose (C-3) (a) D-Aldoses Three carbons Four carbons Five carbons но не HO -OH н-с-он CH, OH D-Glyceraldehyde но-с-н H-C-OH снион D-Threose...
anyone know how to do this? please help if so:) 29. Statements: (1) Cellulose and amylose are glucose polymers which differ in the type of glycosidic linkage present (2) All monosaccharides are either aldoses and ketoses. (3) Enantiomers can never be epimers. a) all three statements are true b) two of the three statements are true c) only one of the statements is true d) none of the statements is true For each of the stereochemical descriptions select from the...
8. For the simplified representation of an enzyme-catalyzed reaction shown below, the statement "ES is in steady-state" means that: ki E+S ES – E+P kit2 a. kz is very slow. b. k1 = k. c. k1 = k-1. d. ki[E][S] = k-1[ES] + ka[ES]. e. ki[E][S] = k-1[ES]. 9. . You are examining the effects of a mutation in the proximal histidine of a heme-containing protein. This mutation has changed the histidine into an alanine. Based on your knowledge of...
1. Which of the following is an aldohexose? 2. Which of the following is a cetopentose? 3. Which of the following best describes the relationship between D-glucose and D-fructose? 4. Which of the following is (are) L-alfohexose(s)? 5. Which of the following aldohexose(s) is (are) dextrorotatory? 6. How many stereoisomers are possible for L-galactose? Draw or look for its structure. 7. Which of the following conpounds is a pair of enantiomers? 8. Draw the fisher projection for L-sedoheptulose and also...