3. Show the Steps necessany to transform the acid an the left into the compound on the Might. Be sure to use Soch.

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**3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl₂.**

a) \[(\text{CH}_3)_3\text{CCH}_2\text{OH} \rightarrow (\text{CH}_3)_3\text{CCH}_2\text{COC}\text{H}_2\text{CH}_2\text{CH}_3\]

b) \[(\text{CH}_3)_3\text{CCH}_2\text{OH} \rightarrow (\text{CH}_3)_3\text{CCH}_2\text{CN(CH}_3)_2\]

**Explanation:** 

For part (a), the transformation involves converting an alcohol (\[\text{OH}\] group) to an ester. This typically involves using reagents such as thionyl chloride (SOCl₂) to convert the alcohol into a more reactive species, which can then be transformed through further reactions. 

For part (b), the alcohol is converted into an amide, which also requires initial activation (often using SOCl₂) and subsequent reactions to achieve the substitution with an amine group.
Transcribed Image Text:**3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl₂.** a) \[(\text{CH}_3)_3\text{CCH}_2\text{OH} \rightarrow (\text{CH}_3)_3\text{CCH}_2\text{COC}\text{H}_2\text{CH}_2\text{CH}_3\] b) \[(\text{CH}_3)_3\text{CCH}_2\text{OH} \rightarrow (\text{CH}_3)_3\text{CCH}_2\text{CN(CH}_3)_2\] **Explanation:** For part (a), the transformation involves converting an alcohol (\[\text{OH}\] group) to an ester. This typically involves using reagents such as thionyl chloride (SOCl₂) to convert the alcohol into a more reactive species, which can then be transformed through further reactions. For part (b), the alcohol is converted into an amide, which also requires initial activation (often using SOCl₂) and subsequent reactions to achieve the substitution with an amine group.
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