Determine the appropriate configuration (R, S, E, or Z) for each of the following compounds. For each structure, write the corresponding configuration in the box drawn

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Determine the appropriate configuration (R, S, E, or Z) for each of the following compounds.
For each structure, write the corresponding configuration in the box drawn

### Understanding Chemical Structures

This section introduces three different chemical structures, allowing you to familiarize yourself with their molecular configurations and functional groups.

#### Compound 1: 

This molecule features a chiral center with a bromine (Br) substituent. It has a base structure of a branched alkane with the formula \[\mathrm{C_{5}H_{8}Br}\]. The key features are:
- An alkyne group (carbon-carbon triple bond) at one end.
- A bromo group (\[\mathrm{Br}\]) attached to the chiral center.

#### Compound 2:

This molecule appears to be a ketone with a hydroxyl group (OH). Its extended carbon chain shows multiple functional groups:
- A six-membered ring with a double bond (indicative of cycloalkene).
- A keto group (C=O).
- A hydroxyl group (\[\mathrm{OH}\]) positioned beta to the ketone.

#### Compound 3: 

This molecule is a simple organic molecule that includes both fluorine (F) and bromine (Br) substituents:
- A chiral center attaches a bromine and a fluorine.
- It has a base structure consistent with a monosubstituted methane derivative.

The boxes beneath each chemical structure are empty, possibly intended for students to fill in with reactions these compounds might undergo, potential products, or other relevant annotations. The exercise encourages active engagement and deeper understanding of molecular structure and reactivity.
Transcribed Image Text:### Understanding Chemical Structures This section introduces three different chemical structures, allowing you to familiarize yourself with their molecular configurations and functional groups. #### Compound 1: This molecule features a chiral center with a bromine (Br) substituent. It has a base structure of a branched alkane with the formula \[\mathrm{C_{5}H_{8}Br}\]. The key features are: - An alkyne group (carbon-carbon triple bond) at one end. - A bromo group (\[\mathrm{Br}\]) attached to the chiral center. #### Compound 2: This molecule appears to be a ketone with a hydroxyl group (OH). Its extended carbon chain shows multiple functional groups: - A six-membered ring with a double bond (indicative of cycloalkene). - A keto group (C=O). - A hydroxyl group (\[\mathrm{OH}\]) positioned beta to the ketone. #### Compound 3: This molecule is a simple organic molecule that includes both fluorine (F) and bromine (Br) substituents: - A chiral center attaches a bromine and a fluorine. - It has a base structure consistent with a monosubstituted methane derivative. The boxes beneath each chemical structure are empty, possibly intended for students to fill in with reactions these compounds might undergo, potential products, or other relevant annotations. The exercise encourages active engagement and deeper understanding of molecular structure and reactivity.
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