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How many 1^(@) amine of the formula C(5)...

How many `1^(@)` amine of the formula `C_(5)H_(13)N` can be used to resolve reacemic 2-methylbutonic acid?

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To determine how many primary amines of the formula C₅H₁₃N can be used to resolve racemic 2-methylbutanoic acid, we can follow these steps: ### Step 1: Understand the Structure of 2-Methylbutanoic Acid 2-Methylbutanoic acid has the following structure: - It consists of a four-carbon chain (butanoic acid) with a methyl group attached to the second carbon. - The molecular formula is C₅H₁₀O₂. ### Step 2: Identify the Required Primary Amines We are looking for primary amines (1° amines) with the formula C₅H₁₃N. A primary amine has the structure R-NH₂, where R is an alkyl group. ### Step 3: Count the Possible Structures for C₅H₁₃N 1. **Positioning the Amine Group**: The amine group can be placed at different positions on the carbon chain. We will consider the following configurations: - **1st Position**: CH₃-CH₂-CH₂-CH₂-NH₂ (Pentylamine) - **2nd Position**: CH₃-CH(CH₃)-CH₂-CH₂-NH₂ (2-Methylbutylamine) - **3rd Position**: CH₃-CH₂-CH(CH₃)-CH₃-NH₂ (3-Methylbutylamine) - **4th Position**: CH₃-CH₂-CH₂-CH(CH₃)-NH₂ (4-Methylbutylamine) 2. **Chirality Consideration**: - For the 2nd position (2-Methylbutylamine), there is a chiral center, which means it can exist as two enantiomers (R and S forms). - For the 4th position (4-Methylbutylamine), there is also a chiral center, which can also exist as two enantiomers. ### Step 4: Calculate the Total Number of Primary Amines - **1st Position**: 1 amine (Pentylamine) - no chirality - **2nd Position**: 2 amines (2-Methylbutylamine) - chiral - **3rd Position**: 1 amine (3-Methylbutylamine) - no chirality - **4th Position**: 2 amines (4-Methylbutylamine) - chiral ### Step 5: Summarize the Total Count Adding these together: - 1 (from 1st position) + 2 (from 2nd position) + 1 (from 3rd position) + 2 (from 4th position) = **6 primary amines**. ### Conclusion Thus, there are a total of **6 primary amines** of the formula C₅H₁₃N that can be used to resolve racemic 2-methylbutanoic acid. ---

To determine how many primary amines of the formula C₅H₁₃N can be used to resolve racemic 2-methylbutanoic acid, we can follow these steps: ### Step 1: Understand the Structure of 2-Methylbutanoic Acid 2-Methylbutanoic acid has the following structure: - It consists of a four-carbon chain (butanoic acid) with a methyl group attached to the second carbon. - The molecular formula is C₅H₁₀O₂. ### Step 2: Identify the Required Primary Amines ...
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