Several reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used. Final Product (3-bromo-2- methyl-2- butanol) Reactant (2-methyl-1- butene) Step 1 Product Step 2 Product Reagent 1 Reagent 2 Reagent 3

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Several reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.

### Multistep Synthesis Pathway from 2-Methyl-1-butene to 3-Bromo-2-methyl-2-butanol

#### Objective:
Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by selecting the appropriate reagents and intermediates. Each bin should only contain one item, and not all provided reagents or structures will be used.

#### Instructional Layout:

1. **Reactant:**
   - **2-Methyl-1-butene**

2. **Reagent 1:**
   - Options: HBr, EtO⁻K⁺, Br₂/H₂O, HBr/ROOR, NBS/ROOR, Br₂

3. **Step 1 Product:**
   - Options: Various intermediate structures (refer to images provided)

4. **Reagent 2:**
   - Options: HBr, EtO⁻K⁺, Br₂/H₂O, HBr/ROOR, NBS/ROOR, Br₂

5. **Step 2 Product:**
   - Options: Various intermediate structures (refer to images provided)

6. **Reagent 3:**
   - Options: HBr, EtO⁻K⁺, Br₂/H₂O, HBr/ROOR, NBS/ROOR, Br₂

7. **Final Product:**
   - **3-Bromo-2-methyl-2-butanol**

#### Detailed Explanation of Image Components:

1. **Reactant Box:**
   - Initial compound structure of 2-methyl-1-butene

2. **Reagent 1–3:**
   - Each box can contain one reagent necessary for the transformation at each step.
   - Possible reagents include:
     - **HBr/CH₂Cl₂:** Hydrogen bromide in dichloromethane
     - **EtO⁻K⁺:** Ethoxide ion with potassium
     - **Br₂/H₂O:** Bromine in water
     - **HBr/ROOR:** Hydrogen bromide with peroxide
     - **NBS/ROOR:** N-bromosuccinimide with peroxide
     - **Br₂:** Bromine

3. **Step 1 & Step 2 Product Boxes:**
Transcribed Image Text:### Multistep Synthesis Pathway from 2-Methyl-1-butene to 3-Bromo-2-methyl-2-butanol #### Objective: Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by selecting the appropriate reagents and intermediates. Each bin should only contain one item, and not all provided reagents or structures will be used. #### Instructional Layout: 1. **Reactant:** - **2-Methyl-1-butene** 2. **Reagent 1:** - Options: HBr, EtO⁻K⁺, Br₂/H₂O, HBr/ROOR, NBS/ROOR, Br₂ 3. **Step 1 Product:** - Options: Various intermediate structures (refer to images provided) 4. **Reagent 2:** - Options: HBr, EtO⁻K⁺, Br₂/H₂O, HBr/ROOR, NBS/ROOR, Br₂ 5. **Step 2 Product:** - Options: Various intermediate structures (refer to images provided) 6. **Reagent 3:** - Options: HBr, EtO⁻K⁺, Br₂/H₂O, HBr/ROOR, NBS/ROOR, Br₂ 7. **Final Product:** - **3-Bromo-2-methyl-2-butanol** #### Detailed Explanation of Image Components: 1. **Reactant Box:** - Initial compound structure of 2-methyl-1-butene 2. **Reagent 1–3:** - Each box can contain one reagent necessary for the transformation at each step. - Possible reagents include: - **HBr/CH₂Cl₂:** Hydrogen bromide in dichloromethane - **EtO⁻K⁺:** Ethoxide ion with potassium - **Br₂/H₂O:** Bromine in water - **HBr/ROOR:** Hydrogen bromide with peroxide - **NBS/ROOR:** N-bromosuccinimide with peroxide - **Br₂:** Bromine 3. **Step 1 & Step 2 Product Boxes:**
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