Part 2 of 2 Identify the isomer of CH100 that has the 13 C NMR spectrum shown. Select the single best answer. CH CH 220 200 180 160 140 120 100 80 60 40 20 o ppm O2,2-dimethylpropanal O3-pentanone O3-methyl-2-butanone O tetrahydropyran O 3-methylbutanal X

Draw the structure of the correct compound on each spectrum and match each type of hydrogen on the structure to the corresponding peak on the spectrum. Thanks

Draw the structure of the compound from the NMR spectra. Mark the peaks that help you find the compound.

The H NMR spectra corresponds to a hydrocarbon with the molecular formula C6H₁4. Deduce the structure from the spectra. Draw the unknown compound. 'H NMR 12 H Select Draw Rings More 1.5 1.4 2 H 1.5 1.0 0.5 0.0 300-MHz H NMR spectrum ppm (8) 0.9 0.8 (CH3)4Si G G Q2E

Annotate the benzophenone and Triphenylmethanol NMR's

Analyse each peak of the H-NMR and 13C-NMR of dibenzalacetone

identify the compound with molecular formula C2H6O that gives this 1H NMR spectrum.

2 Does the NMR match the following product? explain and match each peak with corresponding carbon. I know the NMR photo is not in a good quality but it is the only one i have. Thank you.

A compound with molecular formula C8H8O3 exhibits the following IR, 1H NMR and 13C NMR spectra. Deduce the structure of this compound.

Draw the structure of 2-butanol on the NMR spectrum and assign each peak to the orressponding hydrogen atoms on the molecule.