Question: A compound with a molecular formula C9H10O2 has the following 1H NMR spectrum. Which of the following structures is consistent with this spectrum? A compound with a …

The IR and 1H NMR spectra for Compound X of molecular formula C9H10O2 are shown below (tables of IR and NMR data are attached on the back of the homework). (i) Determine the (? + …

A compound with molecular formula C9H10O2 exhibits a triplet at δ 1.2 (I=3), a quartet at δ 2.6 (I=2), a doublet at δ 7.3 (I=2), a doublet at δ 8.0 (I=2) and a singlet at δ 11 (I=1) in its 1HNMR …

Draw the structure of the compound C9H10O2 from its proton (1H) NMR spectrum below. First-order spin-spin splitting rules and equal coupling constants can be assumed. (Detailed …

Propose a structure for the compound that has the following data: Molecular formula: C9H10O2 13C NMR ? 26.1, 55.3, 113.7, 130.4, 130.5, 163.5, 196.4 ppm. Your solution’s ready to go! …

Question: A H1 NMR spectrum is shown for a molecule with the molecular formula of C9H10O2. Draw the structure that best fits this data A H1 NMR spectrum is shown for a molecule with the …

Question: Given the molecular formula ( C9H10O2 ), the IR spectrum, H NMR, and C NMR attached below, determine the following: - bonds that give rise to the peaks of the IR - …

Draw the structure of the compound C9H10O2 that exhibits the 13C-NMR spectrum below. Impurity peaks are omitted from the peak list. The triplet at 77 ppm is CDCl3.

Question: Identify the unknown compound with the formula C9H10O2 using the following 1H NMR, 13C NMR, and IR spectra. Label all peaks used to make your identification as …

The unknown compound given is C9H10O2 (with 5 degrees of unsaturation). Find the structure of the unknown compound by using the following information: There is a carbonyl peak around …