2. Convert the following line structure into a Fischer projection. ОН ОН HO ОН ОН

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Chapter1: Chemical Foundations
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**2. Convert the following line structure into a Fischer projection.**

- The image shows a structural representation of a molecule. It includes a carbon chain with functional groups: an aldehyde group at one end, three hydroxyl groups attached along the chain, with specific stereochemistry at each chiral center.

**3. Which of the following molecules do you expect to have a higher boiling point, and why? Be sure to mention specific intermolecular interactions.**

- **Molecule A:** Dichloroethane (Cl-CH2-CH2-Cl)
  
- **Molecule B:** Chlorobutane (CH3-CH2-CH2-CH2-Cl)

**Diagram Explanation:**

- Molecule A is depicted with two chlorine atoms bonded to a two-carbon chain, indicating its potential for dipole-dipole interactions due to its symmetrical structure.

- Molecule B is shown as a four-carbon chain with a single chlorine atom, implying weaker intermolecular forces compared to Molecule A.
Transcribed Image Text:**2. Convert the following line structure into a Fischer projection.** - The image shows a structural representation of a molecule. It includes a carbon chain with functional groups: an aldehyde group at one end, three hydroxyl groups attached along the chain, with specific stereochemistry at each chiral center. **3. Which of the following molecules do you expect to have a higher boiling point, and why? Be sure to mention specific intermolecular interactions.** - **Molecule A:** Dichloroethane (Cl-CH2-CH2-Cl) - **Molecule B:** Chlorobutane (CH3-CH2-CH2-CH2-Cl) **Diagram Explanation:** - Molecule A is depicted with two chlorine atoms bonded to a two-carbon chain, indicating its potential for dipole-dipole interactions due to its symmetrical structure. - Molecule B is shown as a four-carbon chain with a single chlorine atom, implying weaker intermolecular forces compared to Molecule A.
Expert Solution
Introduction

In the Fisher projection,bonds which are below the plane of paper are written on right hand side and the bonds which are above the plane of paper are written on the left hand side.Most oxidised group is written on the top.

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