6. Given the ¹H NMR provided, what is the molecule? The molecular formula is C7H₁4O. There is a strong peak in the IR spectrum at 1700 cm¹. Note that the integration line is shown below on the spectrum to show you the ratios of protons in the molecule. • Identify which peak corresponds to which protons on the molecule you drew. You can circle the protons on your molecule and use "2H," "3H," or "9H" to identify which peak belongs to which protons on your molecule. 6 5 4 Chemical shift (8) 3 2H 3H 2 9H 0 (ppm)

6. Given the ¹H NMR provided, what is the molecule? The molecular formula is C7H₁4O. There is a strong peak in the IR spectrum at 1700 cm¹. Note that the integration line is shown below on the spectrum to show you the ratios of protons in the molecule. • Identify which peak corresponds to which protons on the molecule you drew. You can circle the protons on your molecule and use "2H," "3H," or "9H" to identify which peak belongs to which protons on your molecule. 6 5 4 Chemical shift (8) 3 2H 3H 2 9H 0 (ppm)

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

2. Consider the two ¹H NMR spectra sketched below that correspond to the molecule shown. Assign the peaks in each spectrum to the different sets of equivalent protons in the molecule. Why do the spectra for this molecule look different when measured at different temperatures? IN 84°C M 38°C 3 N 1 ppm
The ¹H NMR spectrum of a compound with the formula C12H2406 is pictured below. Determine the structure of the molecule using as much information as possible from the spectrum. Record your calculations and reasoning in the box given below the spectrum 10 9 -00 8 7 T 6 T 5 4 T 3 T 2 1 0
Counterfeit drugs are a common problem in developing regions of the world. Oftentimes, counterfeit pills are made with compounds such as lactose. A lab technician has obtained the IR spectrum shown above for a sample reported to be citalopram, an antidepressant drug. Does the IR spectrum belong to citalopram or lactose? Explain your answer by describing what feature of the IR spectrum confirms your choice and describe what feature is missing from the IR spectrum for the other compound. A. citalopram B. lactose
orgo chem II nmr please help me fill out this chart!
Can anyone help me how to draw a tree diagram a proton A, coupled to three other protons B, C, D, with coupling constants J( AB) = 7Hz, J(AC) = 6Hz, J(AD) = 2Hz, and scale them, and explain your work?
Identify the characteristic seen in the mass spectrum when there is a nitrogen in the compound. There are two molecular ions 2 units apart in a 3:1 ratio. The molecular ion has an even molecular mass. There are two molecular ions 2 units apart in a 1:1 ratio. The molecular ion has an odd molecular mass.
organic chemistry please solve questionnnnnnn 18
3. Protons A-E are identified on the spectrum below and correspond to the five unique protons in the molecule shown. (a) Place all the protons on the molecule and categorize them into Ha, Hb, etc. (b) Fill in the table for this molecule (see answer sheet). E الاس D N PPM B 72 A
Please don't provide handwriting solution
For the dimedone molecule, how many different signals would you see in the proton NMR? Assume you can see them all
b) Propose structures for compounds of the following molecular formulas, using the spectra given below.Show your work
4000 For the following compound identify what peaks would be found in an IR spectrum. Draw the expected IR spectrum on the graph below. Label each peak with the location and portion of the molecule it represents. 3500 3000 IR spectrum 2500 2000 1500 1000 500 0