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xenn [34]
2 years ago
5

The 1h nmr spectra corresponds to an alcohol with the molecular formula c5h12o. Deduce the structure from the spectra.

Chemistry
1 answer:
Sav [38]2 years ago
7 0

Answer:

The question is incomplete. The spectra can be seen in the first picture in the attachment.

The molecule corresponds to the  <em>tert</em>-amyl alcohol.

Explanation:

From the molecular formula, we can calculate the double bond equivalent, to know if there is any <u>unsaturation in the molecule</u>. For a compound of molecular formula CxHyOzXqNp

DBE= (2x+2)- (y+q-p) ÷ 2

DBE= (2.2+2)-12 ÷12 = 0

Therefore, <u>the molecule does not have any unsaturation</u>.

Considering the chemical shift values and the multiplicity, the structure that satisfies the spectra corresponds to the <em>tert</em>-amyl alcohol (structure in attachment).

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