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 molecular formula C 9 H 10 O 2 has the following 1 H NMR spectrum.

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 (? + r) for this compound. Show your work. (ii) Clearly label on the IR spectrum key stretching frequencies with the functional

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 spectrum. What is the structure for this compound?

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 analysis of any non-first order portions of the spectrum will not be required.) Integral ratios to the nearest whole number are (left to right) 1:2:2:2:3.

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! Our expert help has broken down your problem into an easy-to-learn solution you can count on.

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 molecular formula of C9H10O2.

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 - compound name - structure of the compound *note that there are several isomers for this molecular formula --> want to identify the correct one based on the information provided

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 appropriate. Draw the structure of the unknown compound in the box provided.

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 1680cm-1 & OH peak around 3000cm-1, the structure has a pKa of around 8 but tests negative for a carboxylic acid.