H H ÇH2OH ÇH2OH CH2OH H-C-OH НО—С—Н C=0 C=0 C=0 -C-OH H-C-OH H--OH HO–C-H Н-С—ОН –Ċ-OH H-Ċ-OH H-C-OH –C-OH H-C-OH H--OH H-C-OH H-C-OH H-C-OH ČH»OH ČH2OH ČH2OH CH,OH 1 2 3 4 5 Which of the sugars can form furanoses without undergoing isomerization to a different sugar? Select one or more: O a. 1 b. 2 С. 4 d. 5 е. 3 O O O
H H ÇH2OH ÇH2OH CH2OH H-C-OH НО—С—Н C=0 C=0 C=0 -C-OH H-C-OH H--OH HO–C-H Н-С—ОН –Ċ-OH H-Ċ-OH H-C-OH –C-OH H-C-OH H--OH H-C-OH H-C-OH H-C-OH ČH»OH ČH2OH ČH2OH CH,OH 1 2 3 4 5 Which of the sugars can form furanoses without undergoing isomerization to a different sugar? Select one or more: O a. 1 b. 2 С. 4 d. 5 е. 3 O O O
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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Transcribed Image Text:### Topic: Formation of Furanoses
This educational content focuses on the ability of certain sugars to form furanoses without undergoing isomerization to a different sugar. The image depicts five different sugar molecules, each represented by their structural formulas:
1. **Molecule 1**: Features a chain of carbon atoms with hydroxyl (OH) groups attached.
2. **Molecule 2**: Similar structure with variations in the placement of hydroxyl groups.
3. **Molecule 3**: Presents another variation in hydroxyl group structure.
4. **Molecule 4**: Displays a unique arrangement compared to the first three.
5. **Molecule 5**: Contains arrangements mirroring some of the previous molecules' features.
Each molecule is labeled with a number from 1 to 5, indicating different structural configurations ranging from aldoses to ketoses.
#### Question
Which of the sugars can form furanoses without undergoing isomerization to a different sugar?
#### Options
- a. 1
- b. 2
- c. 4
- d. 5
- e. 3
Students should analyze the structural differences to determine which molecules can directly cyclize to form furanoses. Understanding the position of functional groups, particularly the hydroxyl and carbonyl groups, is crucial for identifying potential cyclization pathways.
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