To convert the compound with the formula C10H10O4 into a compound with the formula C10H15N, the reaction you're describing likely involves several steps, with the objective being to remove the oxygen functionalities (likely via reductions) and introduce nitrogen (from the reaction of an amine).
Here’s a simplified version of how this might occur, breaking it down into potential steps:
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Reduction of C10H10O4: The compound C10H10O4 could be reduced to eliminate oxygen-containing functional groups (like esters or carboxylic acids) using hydrogen (H2) in the presence of a catalyst or under acidic/basic conditions to achieve a more hydrocarbon-like compound. The n-l would indicate that you might be using a lithium aluminum hydride-based reduction or a similar reducing agent.
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Ammoniation: Once you’ve reduced your compound to a hydrocarbon or a suitable intermediate like C10H15 (a hydrocarbon base), you can introduce nitrogen through an amination reaction or by reacting with ammonia (NH3) or an amine in the presence of an acid or under basic conditions.
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Neutralization: The use of NaOH in your equation implies that there may be a neutralization step of a protonated amine, leading to the eventual formation of your target compound, C10H15N.
These kinds of transformations are complex and require specific conditions for successful completion, including temperature, pressure, catalysts, and sometimes multiple steps of purification.
Given that this is a hypothetical reaction pathway, specifics about the nature of C10H10O4, the desired substituents, and other detailed conditions would lead to better-defined mechanisms or routes of synthesis. If this chemical transformation is based on a specific synthesis you found, please provide more context or details for a more tailored response.