Indicate what conditions would be required for each reaction shown below in order for the overall conversion to occur. Draw the intermediate product for each step.

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Indicate what conditions would be required for each reaction shown below in order for the overall conversion to occur. Draw the intermediate product for each step. 

This image appears to depict a two-part organic chemical reaction involving different compounds.

**Left Side:**

1. Starting Compound:
   - Structure: A benzene ring attached to a two-carbon chain with a hydroxyl group (OH) and an isopropyl group.
   - Notation: This compound is an aromatic alcohol.

2. Reaction Indicator: A downward arrow suggests a transformation or reaction is occurring.

3. Ending Compound:
   - Structure: The benzene ring is now attached to a carbon with two chlorine atoms (Cl) and an isopropyl group.
   - Notation: This indicates a halogenation reaction, where the original hydroxyl group is replaced by chlorine atoms.

**Right Side (a):**

1. Starting Compound:
   - Structure: Cyclohexane ring with a bromo (Br) and methyl (CH₃) group attached.
   - Notation: This is a bromo substituted cyclohexane.

2. Reaction Indicator: A downward arrow indicates another transformation or reaction.

3. Ending Compound:
   - Structure: Cyclohexane ring with a methyl group and two hydroxyl groups (syn configuration), indicating an addition reaction leading to a diol.
   - Notation: This structure suggests a reaction such as hydroboration-oxidation which typically results in syn stereochemistry.

These transformations suggest typical organic reaction proceedings such as substitution and addition reactions, fundamental concepts in organic chemistry.
Transcribed Image Text:This image appears to depict a two-part organic chemical reaction involving different compounds. **Left Side:** 1. Starting Compound: - Structure: A benzene ring attached to a two-carbon chain with a hydroxyl group (OH) and an isopropyl group. - Notation: This compound is an aromatic alcohol. 2. Reaction Indicator: A downward arrow suggests a transformation or reaction is occurring. 3. Ending Compound: - Structure: The benzene ring is now attached to a carbon with two chlorine atoms (Cl) and an isopropyl group. - Notation: This indicates a halogenation reaction, where the original hydroxyl group is replaced by chlorine atoms. **Right Side (a):** 1. Starting Compound: - Structure: Cyclohexane ring with a bromo (Br) and methyl (CH₃) group attached. - Notation: This is a bromo substituted cyclohexane. 2. Reaction Indicator: A downward arrow indicates another transformation or reaction. 3. Ending Compound: - Structure: Cyclohexane ring with a methyl group and two hydroxyl groups (syn configuration), indicating an addition reaction leading to a diol. - Notation: This structure suggests a reaction such as hydroboration-oxidation which typically results in syn stereochemistry. These transformations suggest typical organic reaction proceedings such as substitution and addition reactions, fundamental concepts in organic chemistry.
Expert Solution
Step 1

Given reaction:

Chemistry homework question answer, step 1, image 1

Step 2

The alkenes can be formed by dehydration of alcohols using dehydrating agent like sulfuric acid.

Alkenes can undergo addition reaction.

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