но- + I2 CHI3 `CH3 methyl ketone excess iodoform carboxylate ion

07) The proton NMR spectrum of a compound with formula C5H12O2 is shown below. THE The carbon-13 NMR spectrum has three peaks, respectively at 15 ppm, 63 ppm and 95 ppm. Based on this information draw the structure of this compound.

draw the structure of the nmr (ethyl acetate) then circle the protons on the structures and correlate the 1H's to the resonances (peaks) on the 1H NMR spectra.

Shown below is th carbon NMR spectrum of a compound of the formula C7H14. The compound decolorizes a solution of bromine in dichloromethane. Assign a structure to this hydrocarbon. Correlation of spectrum with number of hydrogen atoms attached to each carbon=

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Give and explain the H-NMR analysis

Compound A has molecular formula C7H7X. Its 1H-NMR spectrum shows a singlet at 2.26 ppm and two doublets, one at 6.95 ppm and one at 7.28 ppm. The singlet has an integral of three and the doublets each have an integral of two. Its 13C-NMR shows five signals. The mass spectrum of A shows a peak at m/z = 170 and another peak at m/z = 172; the relative height of the two peaks is 1:1 respectively. - Identify what atom X is, explaining your reasoning - Identify Compound A, explaining your reasoning Compound A is treated with a mixture of nitric and sulfuric acids to generate Compound B. The 1H-NMR spectrum of B shows two singlets, one at 2.52 pm and one at 8.13 ppm. The 13C-NMR spectrum of B shows five signals. The mass spectrum of B shows a peak at m/z = 260 and another peak at m/z = 262; the relative height of the two peaks is 1:1 respectively. - Identify compound B, explaining your reasoning Compound B is treated with sodium ethoxide to generate compound C. The 1H-NMR spectrum of C shows…

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Please anotate this NMR

An unknown compound has the formula C4H12O. Elucidate its structure  by scrutinizing its 1H NMR spectra, shown.  Specifically, label each different type of H atom in the final structure with its NMR chemical shift in ppm.