3. Decide whether each pair of formulas represents enantiomers, diastereomers, structural isomers or identical molecules. CH3 CH 3 CH 2OH Br CO2H Br C 'F CH 3"C H H 3C "CO2H CH 2OH H (а) (b) CH 3 CH 3 Br Br CI HO НО OH НО CI Br Br CI -CI F H CH 3 CH 3 (с) (d) OH OH ОН CH 3 H. CH 3 CH 3 H- H NH 2 H H. CI CH 3- НО -CH 20H H CO2H NH 2 НО COH CH 20H OH CI (е) (f) NC CH 3 CH 2OH CH 3 НО CN CH 3 ОН HO „CH 3 H 3C CH 3 H CN НО `CH 2OH CH 20H НО CH 3 НО CN CH 3 CH 2OH (g) (h) CH 3 CH 3 H НО OH H. H H CH 3 ОН CH 3 (i) () 2

Chemistry
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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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Certainly! Below is a transcription and explanation of the image as it would appear on an educational website:

---

**Exercise: Identifying Isomers**

Determine whether each pair of formulas corresponds to enantiomers, diastereomers, structural isomers, or identical molecules.

**Pairs:**

(a)  
- Left: Molecule with a central carbon atom bonded to CH₃, Br, F, and H.
- Right: Same molecule but with a mirror image orientation (as depicted by dashed and wedged bonds).

(b)  
- Left: Molecule with CH₃, H, CO₂H, and CH₂OH attached to a central carbon.
- Right: Molecule with an identical formula but different structural arrangement around the carbon backbone.

(c)
- Left: Cyclopentane ring with Br and F substituents at 1,3 positions, both on wedge bonds.
- Right: Cyclopentane ring with Br and F substituents at 1,3 positions, inverted stereochemistry.

(d)
- Left: Molecule with a central carbon bonded to two Cl atoms and two CH₃ groups.
- Right: Same molecule but with CH₃ and OH substituents in different positions.

(e)
- Left: Three-carbon chain with OH and CO₂H groups in a specific arrangement.
- Right: Similar structural formula with a slightly different arrangement of OH and CO₂H groups.

(f)
- Left: Molecule with a central carbon bonded to OH, Cl, NH₂, and CH₃.
- Right: Identical bonding pattern but different 3D orientation.

(g)
- Left: Molecule with CH₃, CN, and OH around a central carbon.
- Right: Similar structure presented in a different spatial orientation.

(h)
- Left: Cyclohexane ring with CH₃ and CH₂OH substituents.
- Right: Cyclohexane ring with HO and CH₃ substituents in different positions.

(i)
- Left: Cyclopentane ring with OH and H substituents in specific positions.
- Right: Cyclopentane ring with similar substituents in different stereochemical arrangement.

(j)
- Left: Cyclohexane ring with two CH₃ substituents at 1,4 positions.
- Right: Cyclohexane ring with same substituents but different stereochemical positions.

**Explanation:**

For each pair:
- **Enantiomers
Transcribed Image Text:Certainly! Below is a transcription and explanation of the image as it would appear on an educational website: --- **Exercise: Identifying Isomers** Determine whether each pair of formulas corresponds to enantiomers, diastereomers, structural isomers, or identical molecules. **Pairs:** (a) - Left: Molecule with a central carbon atom bonded to CH₃, Br, F, and H. - Right: Same molecule but with a mirror image orientation (as depicted by dashed and wedged bonds). (b) - Left: Molecule with CH₃, H, CO₂H, and CH₂OH attached to a central carbon. - Right: Molecule with an identical formula but different structural arrangement around the carbon backbone. (c) - Left: Cyclopentane ring with Br and F substituents at 1,3 positions, both on wedge bonds. - Right: Cyclopentane ring with Br and F substituents at 1,3 positions, inverted stereochemistry. (d) - Left: Molecule with a central carbon bonded to two Cl atoms and two CH₃ groups. - Right: Same molecule but with CH₃ and OH substituents in different positions. (e) - Left: Three-carbon chain with OH and CO₂H groups in a specific arrangement. - Right: Similar structural formula with a slightly different arrangement of OH and CO₂H groups. (f) - Left: Molecule with a central carbon bonded to OH, Cl, NH₂, and CH₃. - Right: Identical bonding pattern but different 3D orientation. (g) - Left: Molecule with CH₃, CN, and OH around a central carbon. - Right: Similar structure presented in a different spatial orientation. (h) - Left: Cyclohexane ring with CH₃ and CH₂OH substituents. - Right: Cyclohexane ring with HO and CH₃ substituents in different positions. (i) - Left: Cyclopentane ring with OH and H substituents in specific positions. - Right: Cyclopentane ring with similar substituents in different stereochemical arrangement. (j) - Left: Cyclohexane ring with two CH₃ substituents at 1,4 positions. - Right: Cyclohexane ring with same substituents but different stereochemical positions. **Explanation:** For each pair: - **Enantiomers
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