1. Provide compounds consistent with the following data, briefly explain how each piece of data fits withthe compound you provided.a) Compound 1IR data: 1725 cm' (strong)Mass100Spec2850-2950 cm' (medium)80-2.20 ppm (3Н, s)4.12 ppm (2H, s)NMR data: 860 -40-20 -0.0-0.020406080100m/z

Answered: Image /qna-images/answer/059f9e42-7cd1-4fd2-be82-bb7d5f4eda2e.jpg

1. Provide compounds consistent with the following data, briefly explain how each piece of data fits with the compound you provided. a) Compound 1 Mass IR data: 1725 cm' (strong) 100 - Spec 2850-2950 cm-' (medium) 80 - NMR data: 8 2.20 ppm (3H, s) 4.12 ppm (2H, s) 60 - 40 - 20 - 0.0- 0.0 20 40 60 80 100 m/z

1. Provide compounds consistent with the following data, briefly explain how each piece of data fits with the compound you provided. a) Compound 1 Mass IR data: 1725 cm' (strong) 100 - Spec 2850-2950 cm-' (medium) 80 - NMR data: 8 2.20 ppm (3H, s) 4.12 ppm (2H, s) 60 - 40 - 20 - 0.0- 0.0 20 40 60 80 100 m/z

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

a. 2,2,3-trimethylbutane 100 MS-NJ-3103 80 40 20 10 20 30 40 50 60 70 80 90 100 m/z Identify the peaks that give rise to the peaks at m/z 57 and 85. e.g., m/z 85 m/z 57 Relative Intensity
hi there please help me identify the organic compound. thank you compound 19
A student performed a series of reactions and obtained the spectral data provided. The reaction sequence is shown below.. What are the structures for A, B, C, and D? Compound B NMR (relative integrated areas below peaks) CH;CH,O°N 1. BHTHF N-bromosuccnimide A CH;CH,OH B 2. H,O,/OH- D hv reflux Compound A NMR (relative integrated areas below peaks) PPM 5 Compound B IR INFRARED SPECTRUM PPM 5 1 6 0.8 Compound A IR INFRARED SPECTRUM 0.6 0.8 0.4 0.4 0.2- 3000 2000 Wavenumber (cm-1) 1000 The MS of compound B shows an M+ peak at 198 and an M+2 peak at 200 with a relative abundance of 1:0.97 2000 Wavenumber (cm-1) 3000 1000 Transmitance Relative Transmittance
Please provide the structure (drawing) given the IR and NMR spectra.
Please help answering all parts of the following question...thank you! From the following sets of data, please propose a reasonable structure for the unknown organic compound. This molecule is entirely composed of C, H, and N only. Please show all of your work and feel free to write on the spectra any clues as to the structure.
Unknowns for 1H NMR Final Report 10) Chemical Formula: C₁₂H1s (hard to see but, all peaks that integrate to 1H are doublet of doublets) IR: peak at 1650cm-1 2H 10 2H 1H u 7 1H 11) Chemical Formula: C₁0H12O2 IR: strong peak 1720cm-¹ 6 1H 1H 1H 8 12) Chemical Formula: C₂H₂00 IR: strong broad 3300cm-1 5 2H 2H 1H 3 4 PPM 6 PPM -3 septet 1H PPM 9H 6H 18H 0