Using this graphThe peak at 2.0 and 0.9 and 3.4 would be what? Singlet, doubler, triplet or quartet? 1008040006040IR Spectrum(CCle solution)10of base peak2940300013C NMR Spectrum(100.0 MHz, CDCI, solutionproton decoupled957DEPT CH CH₂ CH200¹H NMR Spectrum(200 MHz, CD, solution)MT-88M₁2.08082000120expansionmmm1607m/e1744V (am¹)16016001.061200120C4H802200 240 280ppm8005Mass Spectrumsolvent180|3Problem 4No significant UVabsorption abowa 220 nm402108 (ppm)TMSL08 (ppm)10

سسسلا 4000 100 88898 80 IR Spectrum (CC solution) 60 29 mw 40 3000 13C NMR Spectrum (100.0 MM, CDCI, solution proton decoupled 10 9 DEPT CH CH CH 200 ¹H NMR Spectrum (200 MHz, CD, solution) MT - 88 2.0 80 120 8 2000 1 expansion 160 m/e 7 1744 V (am¹) 160 1600 1.0 200 120 1200 ppm 240 5 800 Mass Spectrum C4H802 280 solvent A 80 4 3 Problem 4 No significant UV Absorption abova 220 nm 40 2 0 1 8 (ppm) TMB 0 8 (ppm)

سسسلا 4000 100 88898 80 IR Spectrum (CC solution) 60 29 mw 40 3000 13C NMR Spectrum (100.0 MM, CDCI, solution proton decoupled 10 9 DEPT CH CH CH 200 ¹H NMR Spectrum (200 MHz, CD, solution) MT - 88 2.0 80 120 8 2000 1 expansion 160 m/e 7 1744 V (am¹) 160 1600 1.0 200 120 1200 ppm 240 5 800 Mass Spectrum C4H802 280 solvent A 80 4 3 Problem 4 No significant UV Absorption abova 220 nm 40 2 0 1 8 (ppm) TMB 0 8 (ppm)

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterL3: Carbon (13c) Nmr Spectroscopy

Section: Chapter Questions

Problem 9CTQ

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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) ppm
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)…
A H1 NMR signal is observed at 117.0 Hz (downfield of TMS) on a 1.20×102‑MHz instrument. a) What is the observed chemical shift in parts per million (ppm)? Chemical shift is ppm b) What is the chemical shift, in parts per million (ppm), if the sample is analyzed with a 60.0‑MHz instrument? Chemical shift is ppm c) Where will the proton signal appear, in hertz, if the sample is analyzed with a 60.0‑MHz instrument?
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) 0.151
plese don't handwritten solution... What MS resolving power is needed to fully resolve the C8H8NO2 and C7H6N2O2 ions (at the base peaks)?
use software to make 1H-NMR and 13C-NMR from the data in the paper and make a table with the following data 1H: chemical shift , multiplet structure, integration, assignment 13C: chemical shift
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Two isomers have NMR chemical shifts of 5.5 and 7.0. What would be the coalescence time in a 500 MHz NMR?
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The 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).