nte 7. D-glucose, blood sugar, exists in two forms; ring open and ring closed. Don’t worry about the chemistry of ring closure (but FYI, arrows are pointing at the atoms involved in this cyclization). This is an example of a problem that has all kinds of irrelevant information that you have to ignore as you search for the actual question. Consider the ring open form of D-Glucose What is the absolute configuration at C-3?How many stereoisomers does the ring open form of D-glucose have? Using Fischer projections, draw its enantiomer and one diastereomerlow many stereoisomers does the ring closed form shown below have? Ring open form KC-l has'y'stereocenters # stereo1somers =? Ring Closed form has s steieo centers :n=5 CHO extract c-3 H- : # steeolsomerj = 2: 32 possble stereoisomeS 2 -OH C-3 = 16 HOH2C HO -H Using Ch 17 Chemistry HO но- 4 OH HO H- 5 DH H- -OH Ring closed B-D-glucose enantiomer of above will have oPP-. Confiq at ench Stereocenter CH2OH O diustereomerof ing open d-gweose reeds to have the same config * and opp config at one or more * ;. numenous eurrect answers Fischer Projection of ring open form of D-Glucose (blood sugar) Will see in chapter 24 g t one ormore CHO C-3 has an s confiquratoon HO CHO HoA + opp here HoH HO Diast. MO + same •H 3.
nte 7. D-glucose, blood sugar, exists in two forms; ring open and ring closed. Don’t worry about the chemistry of ring closure (but FYI, arrows are pointing at the atoms involved in this cyclization). This is an example of a problem that has all kinds of irrelevant information that you have to ignore as you search for the actual question. Consider the ring open form of D-Glucose What is the absolute configuration at C-3?How many stereoisomers does the ring open form of D-glucose have? Using Fischer projections, draw its enantiomer and one diastereomerlow many stereoisomers does the ring closed form shown below have? Ring open form KC-l has'y'stereocenters # stereo1somers =? Ring Closed form has s steieo centers :n=5 CHO extract c-3 H- : # steeolsomerj = 2: 32 possble stereoisomeS 2 -OH C-3 = 16 HOH2C HO -H Using Ch 17 Chemistry HO но- 4 OH HO H- 5 DH H- -OH Ring closed B-D-glucose enantiomer of above will have oPP-. Confiq at ench Stereocenter CH2OH O diustereomerof ing open d-gweose reeds to have the same config * and opp config at one or more * ;. numenous eurrect answers Fischer Projection of ring open form of D-Glucose (blood sugar) Will see in chapter 24 g t one ormore CHO C-3 has an s confiquratoon HO CHO HoA + opp here HoH HO Diast. MO + same •H 3.
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Here is the professor's solution to the problem. However, I do NOT understand the solution. Please explain the answer in a clear step-by-step fashion to me. Explain the answer provided in the image in a clear fashion and as if I did not know much about organic chemistry. It seems to me like the professor is making the problem more complicated than it has to be. Can you demystify or simplify this problem about D glucose?
How can you assign priorities on a Fischer projection? I don't get it.
Here is the complete solution. Please explain it in a basic way.
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