(Wade 5-30) Give the stereochemical relationships between each pair of structures. Examples are same compound, structural isomers, enantiomers, diastereomers. CH3 CH, CH,OH CH,OH CH, CH, НО (c) Н- HO (а) H- ОН НО H- (b) Н- O- НО ОН -H- H- ОН HO-H H -ОН НО -- H ОН CH, CH, CH, CH, CH, CH, CH, Br ОН ОН H. H. H. CH, Br. (f) CH, "CH, (d) (е) H¿C Br H. H Cl `CH, CH ČH3 H H. H CH3 H;C H Br

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**Q2 Relationships**

(Wade 5-30) Give the stereochemical relationships between each pair of structures. Examples are same compound, structural isomers, enantiomers, diastereomers.

**Diagrams and Explanation:**

- **(a)** Two Fischer projections are presented. Each structure includes two methyl (CH₃) groups and hydroxyl (OH) groups. The arrangement of these groups varies between the two diagrams.
- **(b)** Another set of Fischer projections showing two structures with hydroxyl (CH₂OH) groups and OH groups in different configurations.
- **(c)** Fischer projections with two structures having methyl (CH₃) groups and hydroxyl groups arranged differently compared to other examples.
- **(d)** Perspective formulas showing two molecules, each with chlorine (Cl), bromine (Br), and hydrogen (H) attached to a central carbon. Their spatial arrangements differ.
- **(e)** Cyclohexane chair conformations illustrating different placements of methyl and hydroxyl groups on the cyclohexane ring.
- **(f)** Cyclohexane chair conformations showing varied positions of two methyl groups.

Each pair of structures requires analysis to determine their stereochemical relationships, which may include being the same compound, structural isomers, enantiomers, or diastereomers.
Transcribed Image Text:**Q2 Relationships** (Wade 5-30) Give the stereochemical relationships between each pair of structures. Examples are same compound, structural isomers, enantiomers, diastereomers. **Diagrams and Explanation:** - **(a)** Two Fischer projections are presented. Each structure includes two methyl (CH₃) groups and hydroxyl (OH) groups. The arrangement of these groups varies between the two diagrams. - **(b)** Another set of Fischer projections showing two structures with hydroxyl (CH₂OH) groups and OH groups in different configurations. - **(c)** Fischer projections with two structures having methyl (CH₃) groups and hydroxyl groups arranged differently compared to other examples. - **(d)** Perspective formulas showing two molecules, each with chlorine (Cl), bromine (Br), and hydrogen (H) attached to a central carbon. Their spatial arrangements differ. - **(e)** Cyclohexane chair conformations illustrating different placements of methyl and hydroxyl groups on the cyclohexane ring. - **(f)** Cyclohexane chair conformations showing varied positions of two methyl groups. Each pair of structures requires analysis to determine their stereochemical relationships, which may include being the same compound, structural isomers, enantiomers, or diastereomers.
**Q2.5 E**

What is the relationship between the molecules in (e)?

- ☐ same compound
- ☐ structural (constitutional) isomers
- ☐ enantiomers
- ☐ diastereomers
- ☐ completely different

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**Q2.6 F**

What is the relationship between the molecules in (f)?

- ☐ same compound
- ☐ structural (constitutional) isomers
- ☐ enantiomers
- ☐ diastereomers
- ☐ completely different

[Save Answer button]
Transcribed Image Text:**Q2.5 E** What is the relationship between the molecules in (e)? - ☐ same compound - ☐ structural (constitutional) isomers - ☐ enantiomers - ☐ diastereomers - ☐ completely different [Save Answer button] **Q2.6 F** What is the relationship between the molecules in (f)? - ☐ same compound - ☐ structural (constitutional) isomers - ☐ enantiomers - ☐ diastereomers - ☐ completely different [Save Answer button]
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