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Unformatted text preview: potential products are even higher than the m- methylphenoxyacetic acid. This low melting point may have resulted from not being able to adequately dry our final product. Questions: Synthesis for t-butyl methyl ether and n-butyl phenyl ether 2. Yes. This will cause the product, as well as the unreacted phenol, to be in the same layer, rather than separated. The use of K2CO3 will cause the phenol to not be present in the extract. 3. If the isomer dissolves in the aqueous NaOH, it is the A isomer. If the isomer does not dissolve in the aqueous NaOH, it is the B isomer....
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- Spring '09
- Sodium hydroxide, Potassium hydroxide, 0.548 grams, 1.003 grams, 2.029 grams