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Anna11 [10]
3 years ago
15

A compound with the molecular formula C10H10O4 produces a 1H NMR spectrum that exhibits only two signals, both singlets. One sig

nal appears at 3.9 ppm with a relative integration value of 79. The other signal appears at 8.1 ppm with a relative integration value of 52. Draw the structure of this compound.

Chemistry
1 answer:
Kamila [148]3 years ago
8 0

Answer:

The attached figure shows the structure of dimethyl terephthalate.

Explanation:

Dimethyl terephthalate is a compound whose formula is C6H4 (COOCH3) 2. It is a diester produced from terephthalic acid and methanol. It is characterized by being a white solid. Another method for the preparation is from p-xylene and methanol, which is characterized by having an oxidation and an esterification.

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Explanation:

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\textrm{molarity}=\frac{\textrm{moles  of solute}}{\textrm{liters of solution}}

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We have MW (58.44g/mole) and n (0.16 mol), and we need to find m (grams of salt needed) to solve the problem:

\textrm{m} = \textrm{MW * n}= 58.44\frac{\textrm{g}}{\textrm{mol}} * 0.16 \textrm{ mol} = 9.35 \textrm{ g}

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