CHO Pab sldede CHO -HO- motCHO isni ni eslu CHO CH,OH CH3 H. OH H- HO- HOH Sere Br Br- -H H Br H- Br. H- HO- H Br Br Br H HO H H. -Br H- Br Br. Br H- HO- Br H HOH ČH2OH HO- ČH2OH ČH2OH ČH2OH ČH2OH ČH2OH 1 4. 3. I H I 2.

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Convert the following fisher projections into zig zag conformations.

The image depicts a series of six structural formulas of organic molecules, commonly known as monosaccharides. Each structure is numbered from 1 to 6.

1. **Structure 1:**
   - CHO group at the top
   - Four carbon atoms each attached to a hydrogen and a hydroxyl (OH) group
   - Br atom attached to every other carbon and hydrogen atom
   - CH₂OH group at the bottom

2. **Structure 2:**
   - CHO group at the top
   - Four carbon atoms with alternating hydrogen (H) and hydroxyl (OH) groups
   - Br atoms are attached to every other carbon atom
   - CH₂OH group at the bottom

3. **Structure 3:**
   - CHO group at the top
   - Three carbon atoms with alternating hydrogen (H) and hydroxyl (OH) groups
   - Bromine (Br) atoms attached to alternate carbon atoms
   - CH₂OH group at the bottom

4. **Structure 4:**
   - CHO group at the top
   - Three carbon atoms with alternating hydrogen (H) and hydroxyl (OH) groups
   - Bromine (Br) atoms linked to alternate carbon atoms
   - CH₂OH group at the bottom

5. **Structure 5:**
   - CHO group at the top
   - Three carbon atoms with alternating hydroxyl (OH) and hydrogen (H) groups
   - Bromine (Br) atoms linked to alternate carbon atoms
   - CH₂OH group at the bottom

6. **Structure 6:**
   - Different configuration with CHO at the top
   - Each carbon has alternating Br and H arrangement
   - CH₂OH group at the bottom

Each of these structures represents a variant of a monosaccharide molecule, showing different configurations of hydroxyl, bromine, and hydrogen groups around a central carbon chain. These differences in configuration result in varied chemical properties and potential biological functions.
Transcribed Image Text:The image depicts a series of six structural formulas of organic molecules, commonly known as monosaccharides. Each structure is numbered from 1 to 6. 1. **Structure 1:** - CHO group at the top - Four carbon atoms each attached to a hydrogen and a hydroxyl (OH) group - Br atom attached to every other carbon and hydrogen atom - CH₂OH group at the bottom 2. **Structure 2:** - CHO group at the top - Four carbon atoms with alternating hydrogen (H) and hydroxyl (OH) groups - Br atoms are attached to every other carbon atom - CH₂OH group at the bottom 3. **Structure 3:** - CHO group at the top - Three carbon atoms with alternating hydrogen (H) and hydroxyl (OH) groups - Bromine (Br) atoms attached to alternate carbon atoms - CH₂OH group at the bottom 4. **Structure 4:** - CHO group at the top - Three carbon atoms with alternating hydrogen (H) and hydroxyl (OH) groups - Bromine (Br) atoms linked to alternate carbon atoms - CH₂OH group at the bottom 5. **Structure 5:** - CHO group at the top - Three carbon atoms with alternating hydroxyl (OH) and hydrogen (H) groups - Bromine (Br) atoms linked to alternate carbon atoms - CH₂OH group at the bottom 6. **Structure 6:** - Different configuration with CHO at the top - Each carbon has alternating Br and H arrangement - CH₂OH group at the bottom Each of these structures represents a variant of a monosaccharide molecule, showing different configurations of hydroxyl, bromine, and hydrogen groups around a central carbon chain. These differences in configuration result in varied chemical properties and potential biological functions.
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