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: The Molecular Science
5th Edition
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:John W. Moore, Conrad L. Stanitski
Chapter7: Molecular Structures
Section: Chapter Questions
Problem 66QRT
Related questions
Question
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.
Expert Solution
This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
This is a popular solution!
Trending now
This is a popular solution!
Step by step
Solved in 6 steps with 5 images
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Recommended textbooks for you
Chemistry: The Molecular Science
Chemistry
ISBN:
9781285199047
Author:
John W. Moore, Conrad L. Stanitski
Publisher:
Cengage Learning
Chemistry by OpenStax (2015-05-04)
Chemistry
ISBN:
9781938168390
Author:
Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher:
OpenStax
Physical Chemistry
Chemistry
ISBN:
9781133958437
Author:
Ball, David W. (david Warren), BAER, Tomas
Publisher:
Wadsworth Cengage Learning,
Chemistry: The Molecular Science
Chemistry
ISBN:
9781285199047
Author:
John W. Moore, Conrad L. Stanitski
Publisher:
Cengage Learning
Chemistry by OpenStax (2015-05-04)
Chemistry
ISBN:
9781938168390
Author:
Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher:
OpenStax
Physical Chemistry
Chemistry
ISBN:
9781133958437
Author:
Ball, David W. (david Warren), BAER, Tomas
Publisher:
Wadsworth Cengage Learning,
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry: An Atoms First Approach
Chemistry
ISBN:
9781305079243
Author:
Steven S. Zumdahl, Susan A. Zumdahl
Publisher:
Cengage Learning