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- 1. For each set of spectral data, propose an acceptable structure that is consistent with the data. a. MS: M+ m/z=71, IR: 3340, 2960, 2870 cm-1 , 13C NMR: 47.20 (CH2), 25.64 (CH2) ppm b. MS: M+ m/z= 102, IR: 2960, 2870 cm-1, 13C NMR: 72.73 (t), 23.20 (t), 10.80 (q) ppm c. MS: M+ m/z=74, IR: 3310, 2960, 2870 cm^-1, 13C NMR: 62.44 (down), 34.86 (down), 18.98 (down), 13.88 (up) ppm (DEPT-direction) d. MS: M+ m/z=92 (M:M+2=3:1), IR: 2960, 2870 cm^-1, 13C NMR: 67.29 (C), 34.46 (CH3) ppm e. MS:M+ m/z=70, IR: 3070, 2960, 2870, 1666 cm^-1, 13C NMR: 138.92 (t), 114.26 (d), 35.96 (t), 22.17 (t), 13.59 (q) ppm f. MS: M+ m/z= 72, IR: 2960, 2870 cm^-1, 13C NMR: 31.68 (t), 29.80 (d), 22.20 (q), 11.69 (q) ppm g. MS: M+ m/z= 84, IR: 2960, 2870, 1734 cm^-1, 13C NMR: 220.16 (C), 38.30 (CH2), 23.24 (CH2) ppm h. MS:M+ m/z= 138, (M:M+2=1:1), IR: ~3010(broad), 1715 cm^-1, 13C NMR: 173.61(s), 25.21(t) ppm i. MS:M+ m/z=88, IR: 2960, 2870, 1736cm^-1, 13C NMR: 170.95 (C), 60.34 (CH2), 20.98 (CH3), 14.23 (CH3)…For each set of spectral data, propose an acceptable structure that is consistent with the data 1.. MS: M+ m/z=92 (M:M+2=3:1), IR: 2960, 2870 cm^-1, 13C NMR: 67.29 (C), 34.46 (CH3) ppm 2.. MS:M+ m/z=70, IR: 3070, 2960, 2870, 1666 cm^-1, 13C NMR: 138.92 (t), 114.26 (d), 35.96 (t), 22.17 (t), 13.59 (q) ppm 3.. MS: M+ m/z= 72, IR: 2960, 2870 cm^-1, 13C NMR: 31.68 (t), 29.80 (d), 22.20 (q), 11.69 (q) ppmplese don't handwritten solution... What MS resolving power is needed to fully resolve the C8H8NO2 and C7H6N2O2 ions (at the base peaks)?
- For each set of spectral data, propose an acceptable structure that is consistent with that data 1.. MS: M+ m/z= 84, IR: 2960, 2870, 1734 cm^-1, 13C NMR: 220.16 (C), 38.30 (CH2), 23.24 (CH2) ppm 2. MS:M+ m/z= 138, (M:M+2=1:1), IR: ~3010(broad), 1715 cm^-1, 13C NMR: 173.61(s), 25.21(t) ppm 3. MS:M+ m/z=88, IR: 2960, 2870, 1736cm^-1, 13C NMR: 170.95 (C), 60.34 (CH2), 20.98 (CH3), 14.23 (CH3) ppm 4. MS: M+ m/z=73, IR: 3410, 2960, 2870, 1668 cm^-1, 13C NMR: 171.27 (C), 26.26 (CH3), 22.87 (CH3) ppmSpectrophotometric of a Cobalt Chloride Solution Analysis 1. explain in detail the results of this experiment Table 1 Absorption Spectrum of Cobalt Chloride Using a Spectrophotometer Wavelength Absorbance 400 410 420 430 440 450 460 370 480 490 500 510 520 530 540 550 560 570 580 590 600 610 620 630 640 650 660 670 680 690 700 0.036 0.044 0.063 0.095 0.147 0.215 0.284 0.329 0.362 0.402 0.450 0.479 0.464 0.398 0.314 0.216 0.142 0.087 0.054 0.041 0.036 0.036 0.034 0.028 0.030 0.023 0.023 0.023 0.014 0.014 0.011 Test Tube Number Cobalt Chloride Concentration (mol/mL) Absorbance at 510 nm 1 0.000 0.000 2 0.009 0.042 3 0.018 0.92 4 0.027 0.139 5 6 0.036 0.045 0.190 0.236 7 (Unknown) 0.151 ResultsThe NMR spectra for compound 1 were acquired in a 7.5 mg / 0.6 mL solution ofCDCl3 and are found in the accompanying file. The 1H are also listedbelow. Identify the name of compound 1 and Provide a full analysis of the NMR spectra for compound 1 with table showing peak name and assignment 1H NMR (400 MHz, CDCl3) δ 7.73 (d, J = 9.5 Hz, 1H), 7.56 (ddd, J = 8.5, 7.5, 1.6 Hz, 1H),7.51 (dd, J = 7.5, 1.6 Hz, 1H), 7.36 (d, J = 8.5 Hz, 1H), 7.30 (dd, J = 8.5, 7.5 Hz, 1H), 6.45(d, J = 9.5 Hz, 1H).
- MS: m/z=148 (M,100%),149 (11%) IR (liquid film): 3077‐2835 (multitude of weak peaks) 1640(m),1611(m),1511(s),1301(m),1247(s),1176(s),1038(s),922(m),914(m) and 810(m)cm^-1 There are no absorptions in the 3100-‐4000cm^-1 region of the spectrum. (m=medium absorption, s=strong absorption). Choose (circle) the best structure for estragole (W) from the four possible structures (1-4)shown below. Explain briefly how you eliminated each of the incorrect structures for W.Annotate the Mass Spec and 13C NMR for C8H8O2 or 4-Methylbenzoic Acidinterpret NMR spectra and report NMR data stating, in this order: nucleus (1H or 13C), solvent, machine frequency, peaks in order from high to low chemical shift including multiplicity, coupling constants and integration
- what is the purpose y the result of Spectrophotometric of a Cobalt Chloride Solution Analysis? Table 1 Absorption Spectrum of Cobalt Chloride Using a Spectrophotometer Wavelength Absorbance 400 410 420 430 440 450 460 370 480 490 500 510 520 530 540 550 560 570 580 590 600 610 620 630 640 650 660 670 680 690 700 0.036 0.044 0.063 0.095 0.147 0.215 0.284 0.329 0.362 0.402 0.450 0.479 0.464 0.398 0.314 0.216 0.142 0.087 0.054 0.041 0.036 0.036 0.034 0.028 0.030 0.023 0.023 0.023 0.014 0.014 0.011 Test Tube Number Cobalt Chloride Concentration (mol/mL) Absorbance at 510 nm 1 0.000 0.000 2 0.009 0.042 3 0.018 0.92 4 0.027 0.139 5 6 0.036 0.045 0.190 0.236 7 (Unknown) 0.151The molecular ion region of the spectrum of biphenyl. M1 is observed at m/z 154 and the intensity of M 1 1 is 12.9% of M1. What formulas of the type CnHxOyNz are consistent with the spectrum?Spectra data for Unknown Z are listed below. Deduce it's structure. MS: m/z 134 (Molecular Ion) IR: 1720 (strong); 3062 (weak); 2981 (medium); 1605 (medium) 13C NMR and 1H NMR shown on a separate page.