Question: 15. A molecule has the molecular formula C10H12O2. The IR and H-NMR of this compound are provided. Identify the structure of the molecule (Show all of your work and analysis of the spectra).

Given the molecular formula of C10H12O2, IR, proton NMR, and carbon NMR, what would be the structure of this compound? I know it has an unsaturated degree of 5 and has an aromatic ring. Since it does not have -OH group present on the IR, I know it …

Question: Analyze the following proton NMR spectrum for a compound with the chemical structure C10H12O2. Draw the structure of the compound. 1st attempt W See Periodic Table 2H2H

Question: Molecular formula : C10H12O2 Calculate : Degree of unsaturation Assign the peaks for functional groups in the IR Assign the HNMR and CNMR peaks Draw the structure Label the structure with HMNR letters

The proton NMR spectrum for a compound C10H12O2 is shown below along with carbon-13 spectral data in tabular form. (It may be necessary to expand (zoom) some of the 1H signals to view spin-spin splitting details.) The infrared spectrum exhibits a strong band at 1715 cm-1.

Question: Draw the structure of the compound C10H12O2 that exhibits the 13C-NMR spectrum and DEPT data below. Impurity peaks are omitted from the DEPT data list. The triplet at 77 ppm is CDCl3.

A compound with a molecular formula C10H12O2 has the following HNMR spectrum. Which of the following structures is consistent with this spectrum? There are 2 steps to solve this one.

Compound B has the molecular formula C10H12O2. The IR spectrum showed only one major peak in the functional group region around 1740 cm^-1.

Question: Draw the structure for the molecular formula C10H12O2 using the IR and NMR spectra. Draw the structure for the molecular formula C10H12O2 using the IR and NMR spectra. There are 2 steps to solve this one.

The NMR spectrum of C10H12O2 is shown below; the inset is a close-up of the region between 1.6–2.0 ppm. *Draw the structure of C10H12O2 in the box provided. Show transcribed image text