Imagine that you are the quality control analyst supervising the synthesis of aspirin, HC9H,04, a monoprotic acid. One tablet is required to contain 325 mg of aspirin. To analyze your product, you dissolve one tablet in 210. ml H20, then titrate this solution with a 0.1000 M NaOH. You find that 18.06 mL of NaOH solution are required to reach the endpoint. How many mg of aspirin are actually in the tested sample tablet? mg Does this product pass your inspection? (To pass inspection the weight of the tablet must be within 0.5% the required weight.) O Yes O No

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A:

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A:

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A: we know that

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A:

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Q: what is the gas chromatographic analysis based on ?

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Q: None

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A: Discuss the ternary phase diagram.

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