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CH401 Biochemistry I Homework Assignment #6, Carbohydrates 1. Indicate whether each of the following pairs of sugars consists of anomers, epimers, enantiomers, or none of these relationships. a. D-glyceraldehyde and dihydroxyacetone. annos b. D-glucose and D-mannose - epimers c. D-erythrose and L-erythrose er m ers d. a-D-glucose and B-D-glucose - enoshowers e. D-ribose and D-arabinose - f. D-galactose and D-glucose - 2. What does the enzyme mutarotase catalyze? Show by an equation using the glucose isomers. 3. Draw the Haworth...
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.
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.
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...
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...