Part D: A Multi-step Synthesis making (2-methyl-2-hexanol to 2-hexenes)1) IR: discuss the IR, specifically how you can tell the dehydration was successful. Label and discuss key peaks on your spectrum.2) Discuss/analyze NMR; focus your discussion on the peaks arising from the vinylic protons.3) Was the product successfully made? How can you tell? 4000350030002500Wavenumbers (cm-1)2000150010005007072742960.542928.25767880822862.32%Transmittance1454.851376.95886.7984870.3190-825.5892941078.331117.72961649.95983.95790.00 772.48730 842154.19666.91 656.00 647 38 640.97629.65 611.96 605.10 593.89 585.86 579.99 573.78562.20 555.78 549 38 543.93 538.25 531.18 524.96 512.7298673 13623.52505.70102 part D/E ZG.ppg1210SWI: 1015PW:9.7 us8PD: 3.0 sec5.2395.1255.0064.67760.670 29OF1:357.0INA: 12.1122.0161.901LB: 0.01.6951.6011.5181.4111.3902801.2042PTS1d: 81920.8890.7660.5060.000-0.006-0.038PPMUSER: DATE: 11/27/23 (13:46)

Given is a synthesis of 2-hexene from 2-methyl-2-hexanol.Discuss:The IR spectrumAnalyze the NMR spectrumIf the Product was successfully madeThe structure of the product:Analyzing the IR spectrum:FrequencyFunctional Group2960.54-2928.32 cm-1CH stretch 1454.85-1376.95 cm-1C=C stretch886.79 cm-1CH bendThus we can conclude that dehydration has taken place to form the alkene molecule.Analyzing the NMR spectrum:PeaksChemical ShiftMultiplicityIntegrationHa0.9 ppmtriplet3HHb1.44 ppmmultiplet2HHc2.18 ppmmultiplet2HHd2.05 ppmdoublet3HHe5.48 ppmsinglet1HHf5.56ppmtriplet1HThus, we can confirm that the He and Hf are vinylic protons.3. Yes the product was successfully made. We can confirm it by IR and NMr spectrum analysis. All the questions have been answered in steps 2 and 3.