Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For ¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum. Mass Spectrum (not shown): [M] = 343 (100%), 345 (33%) m/z IR Spectrum (not shown): 3031, 2981, 2250 (m), 1601, 1500, 1246 cm¹ (all listed are strong (s) unless otherwise indicated) 1H NMR Spectrum (400 MHz, CDCl3, 25 °C) 8 7 6 5 4 3 2 4H 4H PPM 4H 2H 2H 6H 13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C) (CH) (CH) Q1 (C) (C) (C) (CH2) (CH3) (C) (CH2) (CH2) 160 140 120 100 80 PPM 60 40 40 20 0 14 1/1

Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For ¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum. Mass Spectrum (not shown): [M] = 343 (100%), 345 (33%) m/z IR Spectrum (not shown): 3031, 2981, 2250 (m), 1601, 1500, 1246 cm¹ (all listed are strong (s) unless otherwise indicated) 1H NMR Spectrum (400 MHz, CDCl3, 25 °C) 8 7 6 5 4 3 2 4H 4H PPM 4H 2H 2H 6H 13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C) (CH) (CH) Q1 (C) (C) (C) (CH2) (CH3) (C) (CH2) (CH2) 160 140 120 100 80 PPM 60 40 40 20 0 14 1/1

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

From the given structure, indicate the most stable radical.
Predict and draw the major fragment structures and associated mass of each fragment for the following compounds.
Please examine both of these graphs (Infrared Spectroscopy, and Mass spectroscopy) and determine the bonds, structure, molecular formula and IHD of the unknown organic compound. Please also give reasoning as to why, an explanation would be great. Thank you very much.
Please provide the solution to the attached problem
1. In both the starting material and product the chemical shift of the hydroxyl proton is approximately 13 ppm. Table 22.2 in your “Techniques in Organic Chemistry" textbook gives 4.0 - 8.0 ppm as the typical range for phenolic protons. Explain this apparent discrepancy. Hint: Think about the solvent the NMR spectrum was run in.….
220 200 180 I60 140 120 100 80 20 PPM (+) POk dvea 3 peak area =2 peak 10 PPM
Please Calculate the dipole moment of Glycine molecule using partial charge and positions of atoms.
Questions 23, 24, and 25
3. Explain how LDPE and LLDPE differ in terms of structure, synthesis and properties.
Give detailed Solution with explanation needed..don't give Handwritten answer