Specify the reagent you would use in each step of the following synthesis: a. LIAIH4 b. H₂SO4 c. HCI d. HBr e. SOCI2 OH step 1 step 2 Reagents Available OH f. PBr3 k. CH₂CH₂MgBr g. Dess-Martin periodinane (DMP) 1. C6H5MgBr h. NaH i. NaOH j. CH₂MgBr (phenylmagnesium bromide) m. (CH3)2CHMgBr n. CrO3 Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2

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### Synthesis Reaction: Selection of Reagents

To perform the synthesis shown below, please specify the reagent you would use in each step:

#### Reaction Pathway:
The reaction pathway consists of two steps, starting with the transformation of 2-pentanol.

1. **Step 1:**
   - Starting material: 2-Pentanol (an alcohol)
   - Product: Intermediate compound, shown in the middle.
   
2. **Step 2:**
   - Intermediate compound is converted to the final product, which is 2,2,5-trimethyl-3-hexanol.

#### Reagents Available:
Use the appropriate reagent from the list below for each step:

a. LiAlH₄  
b. H₂SO₄  
c. HCl  
d. HBr  
e. SOCl₂  
f. PBr₃  
g. Dess-Martin periodinane (DMP)  
h. NaH  
i. NaOH  
j. CH₃MgBr  
k. CH₃CH₂MgBr  
l. C₆H₅MgBr (phenylmagnesium bromide)  
m. (CH₃)₂CHMgBr  
n. CrO₃   

#### Instructions:
Specify the reagent by writing the corresponding letter in the boxes below:

**Reagent for Step 1: [__]**  
**Reagent for Step 2: [__]**

#### Graph or Diagram Description:
In this particular problem, there is a chemical structure transformation diagram that shows the starting material 2-pentanol being converted to an intermediate product, and then further to 2,2,5-trimethyl-3-hexanol. The arrows denote the steps and the transformation, with "step 1" and "step 2" clearly labeled.

**The task is to identify the correct reagent needed for each step to achieve the final product.**

This exercise is useful for understanding the application of various reagents in organic synthesis and their specific roles in the transformation of chemical structures.
Transcribed Image Text:### Synthesis Reaction: Selection of Reagents To perform the synthesis shown below, please specify the reagent you would use in each step: #### Reaction Pathway: The reaction pathway consists of two steps, starting with the transformation of 2-pentanol. 1. **Step 1:** - Starting material: 2-Pentanol (an alcohol) - Product: Intermediate compound, shown in the middle. 2. **Step 2:** - Intermediate compound is converted to the final product, which is 2,2,5-trimethyl-3-hexanol. #### Reagents Available: Use the appropriate reagent from the list below for each step: a. LiAlH₄ b. H₂SO₄ c. HCl d. HBr e. SOCl₂ f. PBr₃ g. Dess-Martin periodinane (DMP) h. NaH i. NaOH j. CH₃MgBr k. CH₃CH₂MgBr l. C₆H₅MgBr (phenylmagnesium bromide) m. (CH₃)₂CHMgBr n. CrO₃ #### Instructions: Specify the reagent by writing the corresponding letter in the boxes below: **Reagent for Step 1: [__]** **Reagent for Step 2: [__]** #### Graph or Diagram Description: In this particular problem, there is a chemical structure transformation diagram that shows the starting material 2-pentanol being converted to an intermediate product, and then further to 2,2,5-trimethyl-3-hexanol. The arrows denote the steps and the transformation, with "step 1" and "step 2" clearly labeled. **The task is to identify the correct reagent needed for each step to achieve the final product.** This exercise is useful for understanding the application of various reagents in organic synthesis and their specific roles in the transformation of chemical structures.
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