Write the products of the following sequences of reactions. Refer to your reaction roadmaps to see how the combined reactions allow you to "navigate" between the different functional groups. (a) • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. • Do not draw organic or inorganic by-products. OH 9.8 1. LIAIH4 2. H₂O 3. PCC 4. Br₂, CH3CO₂H ۵۰ []

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Write the products of the following sequences of reactions. Refer to your reaction roadmaps to see how the combined reactions allow you to "navigate" between the different functional groups.

**Reaction Sequence Analysis**

**Objective:** Write the products of the following sequences of reactions. Utilize reaction roadmaps to understand how the combined reactions allow the transformation between different functional groups.

**Instructions:**
- Stereochemistry is not required.
- Explicit drawing of hydrogen atoms is unnecessary.
- Do not include lone pairs; they will not be graded.
- Avoid drawing organic or inorganic by-products.

**Reactions:**

(a) **Substrate:**  
- Compound with a carboxylic acid functional group.

**Reagents:**
1. LiAlH₄
2. H₂O
3. PCC (Pyridinium chlorochromate)
4. Br₂, CH₃CO₂H

**Diagram Component Notes:**
- The substrate is presented as a carboxylic acid with an alkyl chain.
  
**Steps:**
1. **Reduction:** LiAlH₄ is used to reduce the carboxylic acid to a primary alcohol.
2. **Oxidation:** PCC oxidizes the primary alcohol to an aldehyde.
3. **Halogenation:** Br₂ in CH₃CO₂H adds a bromine atom to the alpha carbon of the aldehyde.

The provided diagram window is where the chemical structure transformations are to be depicted without the need for explicit hydrogen atoms or lone pairs, focusing solely on the resulting main organic product.
Transcribed Image Text:**Reaction Sequence Analysis** **Objective:** Write the products of the following sequences of reactions. Utilize reaction roadmaps to understand how the combined reactions allow the transformation between different functional groups. **Instructions:** - Stereochemistry is not required. - Explicit drawing of hydrogen atoms is unnecessary. - Do not include lone pairs; they will not be graded. - Avoid drawing organic or inorganic by-products. **Reactions:** (a) **Substrate:** - Compound with a carboxylic acid functional group. **Reagents:** 1. LiAlH₄ 2. H₂O 3. PCC (Pyridinium chlorochromate) 4. Br₂, CH₃CO₂H **Diagram Component Notes:** - The substrate is presented as a carboxylic acid with an alkyl chain. **Steps:** 1. **Reduction:** LiAlH₄ is used to reduce the carboxylic acid to a primary alcohol. 2. **Oxidation:** PCC oxidizes the primary alcohol to an aldehyde. 3. **Halogenation:** Br₂ in CH₃CO₂H adds a bromine atom to the alpha carbon of the aldehyde. The provided diagram window is where the chemical structure transformations are to be depicted without the need for explicit hydrogen atoms or lone pairs, focusing solely on the resulting main organic product.
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