Draw the Fischer projection from the Haworth projection shown below. Н CH2OH I он – OH ОН Н I OH

Chemistry: The Molecular Science
5th Edition
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:John W. Moore, Conrad L. Stanitski
Chapter10: Fuels, Organic Chemicals, And Polymers
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**Question 24 of 29:**

Draw the Fischer projection from the Haworth projection shown below.

**Diagram:**

The diagram on the left side of the screen displays a Haworth projection of a cyclic sugar molecule. Here are the details:

- The molecule forms a hexagonal ring structure.
- The top of the ring has a –CH₂OH group.
- The ring consists of five carbon atoms and one oxygen atom.
- Various hydrogen atoms (H) and hydroxyl groups (OH) are attached to the carbon atoms around the ring.

**Instructions to the student:**

Please select a drawing or reagent from the question area to convert the given Haworth projection into a Fischer projection. The Fischer projection is a linear depiction of the molecule, emphasizing the stereochemistry of the stereocenters.

**Note:**

To complete this task, ensure that you accurately convert the stereochemistry of each carbon atom from the Haworth to the Fischer projection format. The Fischer projection places the carbon backbone vertically, with horizontal lines representing bonds projecting toward the viewer.
Transcribed Image Text:**Question 24 of 29:** Draw the Fischer projection from the Haworth projection shown below. **Diagram:** The diagram on the left side of the screen displays a Haworth projection of a cyclic sugar molecule. Here are the details: - The molecule forms a hexagonal ring structure. - The top of the ring has a –CH₂OH group. - The ring consists of five carbon atoms and one oxygen atom. - Various hydrogen atoms (H) and hydroxyl groups (OH) are attached to the carbon atoms around the ring. **Instructions to the student:** Please select a drawing or reagent from the question area to convert the given Haworth projection into a Fischer projection. The Fischer projection is a linear depiction of the molecule, emphasizing the stereochemistry of the stereocenters. **Note:** To complete this task, ensure that you accurately convert the stereochemistry of each carbon atom from the Haworth to the Fischer projection format. The Fischer projection places the carbon backbone vertically, with horizontal lines representing bonds projecting toward the viewer.
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