Unknown 3 ¹H NMR data (ppm) multiplicity integration 0.86 t 3 1.50 2 2.02 2 6.71 1 7.24 1 sextet t S

Analyze the 13C NMR spectrum for the C5H1CI compound shown below and determine a structure. Assign all the carbons. Chemical Shift(ppm) Multiplicity 57.3 triplet 33.1 singlet 27.3 quartet

Draw the splitting pattern and assign and label the H of the spectrum of C4H8O

18. Proton NMR spectra are given together with molecular formula. Propose a structure that corresponds to each spectrum. (Hint: Find IHD first). Assign peaks to show which protons give rise to which peaks 10 10 10 (b) C4H8O₂ Offset: 2.4 ppm (b) C₂H100 9 (c) CsHgO₂ 9 8 8 7 7 6 6 6 5 8 (ppm) OHz 5 8 (ppm) 4 3.08 2.98 2.88 2.78 8 (ppm) 50Hz 4 4 3 2 1 0 0

NMR data Summary NMR solvent: DMSO-d6 'H NMR: Splitting (Multiplicity) Integration Chemical Shift 9.67 singlet 1H singlet doublet 9.17 7.37 6.72 2.00 1H 2H doublet singlet 2H 3H 1"C NMR: Chemical Shift 167.8 153.3 131.1 121.1 115.1 23.8 15N NMR: Chemical Shift 132.3 Instructions: Step 0: Look at the structure of Tylenol. Determine integration, and splitting you are expecting in the 'H NMR. Step 1: Look at the integration and splitting of the signals in the H NMR spectrum - assign the chemical shift of the protons of the methyl group; make a note which signals in the 'H NMR are due aromatic protons, NH and/or OH. Step 2: Look at the 'HSN HSQC spectrum - Use this spectrum to assign the chemical shifts of the NH proton and the OH proton. Step 3: Look at the 'H1SN HMBC spectrum - Use this spectrum to assign the chemical shifts of the aromatic protons in the 'H NMR. Step 4: Look at the 13C NMR spectrum - Make a note which carbon atoms are aromatic and/or alkyl. Assign the chemical shift of…

What is the structure of the compound with molecular formula C5 H10 O

Step-by-step solution

Can you explain the IR spectrum ?