Which of the following reactions would produce this product? Select ALL correct answers. он 1. CH3MGB 2. CH,CH MgBr 3. HCI, H2O 1. PhLi b) 2. HCI, H20 1. CH3CH2MgBr 2. HCI, H,O c) of 1. CH3CH2LI 2. HC, H.о d)

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Which of the following reactions would produce this product? Select ALL correct answers.

### Question

**Which of the following reactions would produce this product? Select ALL correct answers.**

**Product Structure:**
- A benzene ring with a secondary alcohol group attached to a two-carbon chain.

### Reaction Options

**a)** 
1. Reagent: CH₃MgBr
2. Reagent: CH₃CH₂MgBr
3. Workup: HCl, H₂O

- Structure: Benzophenone derivative (benzene ring with a ketone group, C=O).

**b)** 
1. Reagent: PhLi
2. Workup: HCl, H₂O

- Structure: Propanone derivative (simple aliphatic ketone, C=O with two methyl groups).

**c)** 
1. Reagent: CH₃CH₂MgBr
2. Workup: HCl, H₂O

- Structure: Benzophenone derivative (similar structure as in option a).

**d)** 
1. Reagent: CH₃CH₂Li
2. Workup: HCl, H₂O

- Structure: Benzophenone derivative (similar structure as in option a).

### Explanation of Diagrams

- Each diagram shows a benzene ring attached to different carbonyl or alkyl groups, with specific reagents used to induce reactions that could potentially lead to the formation of the depicted alcohol product.
- The Grignard reagents (RMgBr) and organolithium reagents (RLi) are used in attempts to form new carbon-carbon bonds, which, after protonation, might result in the formation of alcohols.

Please determine which options correctly convert the given starting material into the specified product.
Transcribed Image Text:### Question **Which of the following reactions would produce this product? Select ALL correct answers.** **Product Structure:** - A benzene ring with a secondary alcohol group attached to a two-carbon chain. ### Reaction Options **a)** 1. Reagent: CH₃MgBr 2. Reagent: CH₃CH₂MgBr 3. Workup: HCl, H₂O - Structure: Benzophenone derivative (benzene ring with a ketone group, C=O). **b)** 1. Reagent: PhLi 2. Workup: HCl, H₂O - Structure: Propanone derivative (simple aliphatic ketone, C=O with two methyl groups). **c)** 1. Reagent: CH₃CH₂MgBr 2. Workup: HCl, H₂O - Structure: Benzophenone derivative (similar structure as in option a). **d)** 1. Reagent: CH₃CH₂Li 2. Workup: HCl, H₂O - Structure: Benzophenone derivative (similar structure as in option a). ### Explanation of Diagrams - Each diagram shows a benzene ring attached to different carbonyl or alkyl groups, with specific reagents used to induce reactions that could potentially lead to the formation of the depicted alcohol product. - The Grignard reagents (RMgBr) and organolithium reagents (RLi) are used in attempts to form new carbon-carbon bonds, which, after protonation, might result in the formation of alcohols. Please determine which options correctly convert the given starting material into the specified product.
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