Sol:
To indicate the given following sugars belong to anomer, epimers, enantiomers or none of these, we need to know the definition of all these.
D-glyceraldehyde and Dihydroxyketone posses none of the given relationship as they are Aldo-ketose.
CH401 Biochemistry I Homework Assignment #6, Carbohydrates 1. Indicate whether each of the following pairs of...
4 and 5 .320dit-C to arriol 92006Tyq bris 92001Tt- od ws7C. obitedoobeib gniwollot dt hot (mot toda bas gftol) smise pitbra1912y2 9dt svið .a но,НО HO,HO HO HO CH401 Biochemistry I Homework Assignment #6, Carbohydrates 1. Indicate whether each of the following pairs of sugars consists of anomers, cpimers, enantiomers, or none of these relationships. a. D-glyceraldehyde and dihydroxyacetone - anomos b. D-glucose and D-mannose - epimers c. D-erythrose and L-erythrose - er hurts d. a-D-glucose and B-D-glucose - ena...
2. What does the enzyme mutarotase catalyze? Show by an equation using the glucose isomers. 3. Draw the Haworth structures of the following monosaccharides: D-glucopyranose, L- glucopyranose, D-glucofuranose, D-mannopyranose, D-galactopyranose, D-deoxy- ribofuranose, D-fructofuranose, D-fructopyranose. For the purposes of this problem, ignore the distinction betweena and B.
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...
21. Which of the following is not a function of carbohydrates? A) They are catalytic components of enzymes B) They play key roles in processes that take place on the surface of cells C) They are major energy sources D) They are used in structural roles Section: 11.1 22. Carbohydrates are A) aldehydes with two or more hydroxyl groups C) acids with two or more hydroxyl groups E) A and B B) ketones with two or more hydroxyl groups D)...
Please choose the correct answer: Question 1 1 pts CH-оH -о он ОН, ОН ОН The molecular above is? alpha glucopyranose beta glucofuranose alpha fructofuranose alpha galactopyranose beta fructopyranose beta galactopyranose alpha glucofuranose beta glucopyranose Question 2 1 pts CHO Он Н OH н. н -ОН CH,он The molecule above is? galactose fructose glucose mannose ribose OOOO Question 3 1 pts СНо Н -ОН OH Н н Он CH2OH The furanose form of this molecule is which of the structures...
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...
18. Which of the following compound(s) would undergo mutarotation in aqueous solution? 19. Draw the chair conformation of a-D-galactopyranose. 20. Which of the following compound(s) is a glycoside? 21. Provide the reagents neccesary to carry out the following conversion. 22. Predict the product(s) for the following reaction. 23. D-glucose & D-galactose are ______epimers of each other. 24. Predict the product(s) for the following reaction. 25. Which of the following compound(s) would produce D-glucose and D-mannose when treated with HCN followed...