b. What is the experimental integration ratio in the H-NMR data that you obtained? Is this ratio consistent with the expected integration ratio of the pure product?

c. According to the H-NMR data, is the sample you prepared pure?

d. Label the peak in the H-NMR spectrum a, b, c etc. starting with the most uplift peak. Draw the structure of 4-BENZOXY-3-METHOXYBENZALDEHYDE and label each proton a, b, c etc. accordingly. According the multiplicity for all of the non-equivalent protons

Transcribed Image Text:

8.18 3.00 1.88 p.96 0.51 PPM 14 12 10 USER: -- DATE: 07/27/21 (16:05) OF1: 368.3 NA: 1 PTS1:: 8192 FI: 60.010 EX: c:left HIVGppg SWI: 1000 PW: 8.2 us PD: 3.0 sec LB: 0.0 Nuts - temp 9.834 E6E'L 5.241 3.943 1.642 8.18 3.00 1.88 p.96 0.51 PPM 14 12 10 USER: -- DATE: 07/27/21 (16:05) OF1: 368.3 NA: 1 PTS1:: 8192 FI: 60.010 EX: c:left HIVGppg SWI: 1000 PW: 8.2 us PD: 3.0 sec LB: 0.0 Nuts - temp 9.834 E6E'L 5.241 3.943 1.642

Answer rating: 100% (QA)

b What is the experimental integration ratio in the HNMR data that you obtained There a... View the full answer