Using a Fisher projection, draw all of the possible D-stereoisomers of glucose. List all of the enantiomers, diastereomers, and epimers for glucose and galactose.
Using a Fisher projection, draw all of the possible D-stereoisomers of glucose. List all of the...
of each other. 36.) Glucose and galactose are A) anomers B) enantiomers C) epimers D) cis-trans isomers of D-glucose. 37.) D-galactose and D-talose are A) diastereomers B) epimers C) enantiomers D) cis-trans isomers
of each other. 36.) Glucose and galactose are A) anomers B) enantiomers C) epimers D) cis-trans isomers of D-glucose. 37.) D-galactose and D-talose are A) diastereomers B) epimers C) enantiomers D) cis-trans isomers
9. Using Fisher projections, draw all of the possible stereoisomers for 3,4- difluorohexane. For each stereoisomer, determine the absolute configuration for each stereogenic carbon. Then, determine the relationship between each set of stereoisomers. (25 points)
Ch. 15 Carbohydrates 1) How many stereocenters are in: a) Glucose b) Fructose c) Galactose 2) Area-D-glucose and B-D-glucose anomers? Are they enantiomers? Explain 3) Draw Haworth structure of B-D-galactose and B-D-fructose. 4) Convert each Haworth projection to a Fisher projection
1) Monosaccharide Structures r str s, show the carbon atom numbers. A. Fisher projection of D-glucose B. Haworth projection of β-D glucose C. chair representation of β-D glucose in its most favorable conformation | D. Fisher projection of D-Fructose E. Fisher projection of C3 epimer of D F. Haworth Projection of C3 epimer of D- glucose glucose
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...
Draw all the stereoisomers (redraw the first with the proper 3-D
representation) of the compounds below. The configuration for the
first isomer you should draw is provided. Assign R or S
configuration to each chirality center in the additional isomers.
Indicate the stereochemical relationship (diastereomers,
enantiomers, meso compounds) between the first isomer and each of
the others. The configuration for the Fischer Projection has been
omitted, since stereochemistry can be determined from a 2-D
structure. You do not need to...
Report Sheet A.2 Fischer projection of D-glucose Haworth (cyclic) formulas B-D-glucose Q-D-glucose Bouwbedeus A.3 Fischer projection of D-fructose Haworth (cyclic) formula for C-D-fructose Fischer projection of D-galactose Haworth (cyclic) formula for a-D-galactose Questions and Problems Q.1 How does the structure of D-glucose compare to the structure of D-galactose?
10. The structure of glucose is listed below. Draw C-3 and C-5 epimers CHO 11. Consider the six compound pairs below and label them as enantiomers, epimers, diastereomers, but not epimers, constitutional isomers, or identical compounds. ???? -? a. A and Bb. Aand C c. Band C d. Aand D e. Eand F
Draw all stereoisomers associated with 2-Bromo-3-methypentane.
Draw the Fischer projections for all stereoisomers associated with
2-Bromo-3-methypentane. Clearly label all stereoisomers as either
enantiomers, diastereomers, or meso. Place the lowest priority
groups in two vertical positions in final display. SHOW ALL WORK
CLEARLY. Thank you!