Answer Happy

7. Analyze and characterize the ¹H NMR spectrum of your ester and report the data below according to JACS format. Attach the spectrum with each peak labeled. Draw your structure below with the corresponding H's labeled. Does any starting material remain according to your spectrum? Explain.
5.0 4.0 66'1 3.0 3.00 2.0 1.99 1.0 90 € Unknown alcohol A JEOLO Filename Author Experiment Sample Id Solvent Actual Start Time Revision Time Data Format Din_Size X_Domain Din Title Dim Unite Dimensions Site Spectrometer Field Strength X Acq Duration X Domain X Freq X_offset X Points X Points Input x Prescans X Resolution X Sweep X Sweep Clipped X Sweep Input Irr Domain IKE_Freq Irr Offset Tri Donain Tri Freq Tri Offset Blanking clipped Scans Total_Scans Relaxation Delay Reeve Gain Temp Get x 90 Width X Acq Time x Angle x Atn X_Data_Points x Points Default X Pulse IFE Mode Tri Mode Dante Loop Dante Presat Decimation Rate Default X Resolution Experiment Path Initial Wait Phase Presat Time Presat Tine Flag Relaxation Delay Cale Relaxation Delay Default Relaxation Delay Default_Tem = 68_PROTON-1- albgroup single pulse 68 CHLOROFORM-D - 5-JUL-2022 6-JUL-2022 = 1D COMPLEX - 26214 - Proton = Proton (ppm) - X = NMR-1 - JNX-ECZ4008/ = 9.38742128 (T -2.000132161 - Proton = 399.68236879 = 5(ppm) - 14989 - 11991 <-0 -0.49996696[H] = 7.4940048 [k -5.99520384 [k = 14 (ppm) - Proton - 399.68236879 - 5(ppm) ■ Proton - 399.68236879 = 5(ppm) = 2.0[us] = FALSE =16 16 - 4[0] - 32 = 21.4[dc] <-5.0[us] = 2.00013216 [a - 45[deg) = 4.7[dB] 32768 - 24981 - 2.9[us] - Off - off <<-400 = FALSE -0 = 0.3[Hz] - e:\Program F <= 1(a) -(0, 90, 270, <- 4[0] = FALSE - 0[] 4.99986784 [a 7(a)