Draw the Fischer projection from the Haworth projection shown below. H OH CH₂OH OH н н OH Н OH

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Draw the Fischer projection from the Hawthorne projection show below. 

**Question:**

Draw the Fischer projection from the Haworth projection shown below.

**Diagram Description:**

The diagram depicts a Haworth projection of a six-membered ring representing a cyclic sugar molecule. The specific structure appears to be a glucopyranose:

- The ring is hexagonal with an oxygen atom at the top right vertex.
- The carbon atoms are not numbered, but starting from the right and going clockwise, each carbon is bonded to either an OH group or a hydrogen atom.
- At the top left vertex, there is a CH₂OH group extending upwards.
- Hydroxyl (OH) groups are attached to each carbon in a specific pattern, indicating the stereochemistry of the sugar.
- The pattern of OH groups descends from the top right as: hydrogen (H) down, OH down; then OH down, hydrogen (H) up; next OH up, H down; and finally OH down, H up before the repeat.
- Each carbon also has a single bonded hydrogen atom opposite to the hydroxyl groups.

**Instructions:**

- Convert the given cyclic (Haworth) structure into its corresponding Fischer projection, maintaining the stereochemistry indicated by the positioning of OH and H groups.

**Additional Notes:**

- Fischer projections are a two-dimensional representation of a molecule's 3D structure, often used for sugars.
- In the Fischer projection, the longest carbon chain is drawn vertically with the most oxidized group (often the aldehyde or ketone group) at the top.
- Horizontal lines represent bonds coming out of the plane, while vertical lines are bonds going into the plane.
Transcribed Image Text:**Question:** Draw the Fischer projection from the Haworth projection shown below. **Diagram Description:** The diagram depicts a Haworth projection of a six-membered ring representing a cyclic sugar molecule. The specific structure appears to be a glucopyranose: - The ring is hexagonal with an oxygen atom at the top right vertex. - The carbon atoms are not numbered, but starting from the right and going clockwise, each carbon is bonded to either an OH group or a hydrogen atom. - At the top left vertex, there is a CH₂OH group extending upwards. - Hydroxyl (OH) groups are attached to each carbon in a specific pattern, indicating the stereochemistry of the sugar. - The pattern of OH groups descends from the top right as: hydrogen (H) down, OH down; then OH down, hydrogen (H) up; next OH up, H down; and finally OH down, H up before the repeat. - Each carbon also has a single bonded hydrogen atom opposite to the hydroxyl groups. **Instructions:** - Convert the given cyclic (Haworth) structure into its corresponding Fischer projection, maintaining the stereochemistry indicated by the positioning of OH and H groups. **Additional Notes:** - Fischer projections are a two-dimensional representation of a molecule's 3D structure, often used for sugars. - In the Fischer projection, the longest carbon chain is drawn vertically with the most oxidized group (often the aldehyde or ketone group) at the top. - Horizontal lines represent bonds coming out of the plane, while vertical lines are bonds going into the plane.
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