Deduce the structure of an unknown compound using the data below: Molecular Formula: C6H12O IR: 1705 cm-1 1H NMR: no absorptions
greater than δ 3 ppm 13C NMR: δ 24.4, δ 26.4, δ 44.2, and δ 212.6 ppm. Resonances at δ 44.2 and 212.6 have very low intensity.
1 answer:
Answer:
The compound elucidated from the spectral data is <u>4-methyl penta-2-none</u>
Explanation:
- <u>1700 cm-1 from IR data</u> suspects aldehyde/ketone or carboxylic acid. However,since the peak is not a stretched vibration, it implies an aldehyde or ketone present.
- <u>3 ppm H NMR</u> confirms O-CH3 bond
- <u>24.4 13C NMR</u> confirms CH3-R bond
- 26.4 13C NMR confirms H3C-(R)C(H)-R
- 44.2 13C NMR Confirms C=
- 2126 13C NMR confirms aldehyde C=O bond
<u>The deduced structure is 4-methyl penta-2-one (see attached) </u>given multiple CH3 atoms.
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Answer: 0.151
Explanation:
Rate law says that rate of a reaction is directly proportional to the concentration of the reactants each raised to a stoichiometric coefficient determined experimentally called as order.
The rate in terms of reactants is given as negative as the concentration of reactants is decreasing with time whereas the rate in terms of products is given as positive as the concentration of products is increasing with time.
Given:
Putting in the values we get:
Thus the rate of appearance of is 0.151