Question

please answer completely and correctly

8) The H and C NMR spectra of a compound with the formula CHoBr are shown below. Pr a structure for this molecule and assign the peaks in the spectra. TMS 10 9 0 ppm Chemical shift (5) TMS 200 180 16010 120 10806040 20 ppm Chemical shift (8) 9) The mass spectrum and 13C NMR spectrum of a hydrocarbon are shown below. Propose a structure for this hydrocarbon and explain your answer based on the spectral data. 100 80 60 40 20 10 20 40 60 80 100 120 140 TMS 180__160- ㅡㅡ 100ㅡㅡ 80- -40- 20 200 140 120 60 0 ppm Chemical shift (6)

media%2F627%2F6273034f-8376-4a73-89cf-d9

0 0
Add a comment Improve this question Transcribed image text
Answer #1

nepvuoL w.dehu, vch.a. : Pri-9/.-- Hen poss n Ct) 4:21 a. 댜 CS) S) (S)

C44 i- Pr O. C. G1 22 13y 1구. C :

I am not sure with 9th problem sorry.

@ Please rate the solution

Add a comment
Know the answer?
Add Answer to:
please answer completely and correctly 8) The 'H and "C NMR spectra of a compound with...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • Deduce the following structure of the compound given their IR, H1 NMR, 13C NMR spectra, and...

    Deduce the following structure of the compound given their IR, H1 NMR, 13C NMR spectra, and assign IR functional group absorptions and assign the structure's protons and carbons to their respective spectral resonances. Compound 6 1756 IR Spectrum uid Sm) 15820 4000 3000 2000 1600 1200 800 V (cm) 100 55 Mass Spectrum 71 80 70 60 No significant UV M158 (1%) absorption above 220 nm C&H140s 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz,...

  • 13C NMR 1. Propose a structure for the compound CsH12, with the following 13C NMR spectral...

    13C NMR 1. Propose a structure for the compound CsH12, with the following 13C NMR spectral data. 160 140 120 80 60 40 20 0 200 180 CDS-00-748 100 ppm 2. Propose a structure for the compound CaH;Br, with the following C NMR spectral data. 200 180 160 140 120 80 60 40 100 ppm 20 0 3. Propose a structure for the compound C H2O2, with the following "'C NMR spectral data. 200 180 160 140 120 30600 T...

  • Deduce the following structure of the compound given their IR, H1 NMR, 13C NMR spectra, and...

    Deduce the following structure of the compound given their IR, H1 NMR, 13C NMR spectra, and assign IR functional group absorptions and assign the structure's protons and carbons to their respective spectral resonances. Compound 4 Da- U6)+20 IR Spectrum Oquid fim) 1760 800 1200 2000 1600 3000 4000 v (cm) Mass Spectrum 100 43 No significant UV absorption above 220 nm M146 (1% ) 87 20 CH1004 280 40 80 120 m/e 160 200 240 13C NMR Spectrum (1000 MHz,...

  • Please answer questions 2,3, and 4 that correspond to the nmr spectra of (2E,6E)-2,6-dibenzylidenecyclohexanone. Product: ppm...

    Please answer questions 2,3, and 4 that correspond to the nmr spectra of (2E,6E)-2,6-dibenzylidenecyclohexanone. Product: ppm BE 06 135 94 190 180 170 160 150 140 130 120 110 100 90 80 70 60 50 40 ppm 30 20 2. Are there any non-aromatic or non-alkene protons seen on the 'H NMR spectrum (yes or no)? If so, list the corresponding ppm value(s): 3. Are there any peaks upfield of 70 ppm seen in the 13C NMR spectrum (yes or...

  • The 1H-NMR and 13C-NMR spectra of an unknown compound (formula C8H10) are shown below. Draw the structure of the unknown...

    The 1H-NMR and 13C-NMR spectra of an unknown compound (formula C8H10) are shown below. Draw the structure of the unknown compound. The total integration of the peaks at around 7 ppm is 4. The integration of the peak at around 2 ppm is 6. 7 6 5 4 3 ppm TTTTTTTTTTTTTTTT 200 180 160 140 120 100 80 60 40 20 0 pom CH3 Create OscerSketch Answer 8 Incorrect: Answer has an incorrect structure.

  • In the boxes below, provide the structure of the compound that corresponds to each set of spectra...

    In the boxes below, provide the structure of the compound that corresponds to each set of spectra on the next 5 pages. Be sure to show your work on the spectra for full credit. Account for all numbered peaks in the IR. In peaks if necessary. Assign all NMR spectra as completely as possible: number of NMR signals, integration, chemical shift, and splitting the mass spectrum, determine degrees of unsaturation and label 4 IR Spectrum 3000 2000 1 1600 1200...

  • On the attached image are 1H NMR, 13C NMR, and IR spectra of a compound with...

    On the attached image are 1H NMR, 13C NMR, and IR spectra of a compound with the formula C4H8O. 1H NMR signal at 1.2 is caused by 3 hydrogens, the sigbal at 2.1 is caused by 3 hydrogens, and the signal at 2.5 is caused by 2 hydrogens. Identify the compound. CH 1110 9 8 7 6?4 Problem 6. 'H NMR spectrum of compound HsO Problem 6. 13C NMR spectrum of compound C4HsO 200 180 160 140 120 100 80...

  • The following slides contain 1H and 13C-NMR spectra as well as GC/MS spectra for compound 2...

    The following slides contain 1H and 13C-NMR spectra as well as GC/MS spectra for compound 2 shown below. After analyzing the spectra, assign all proton and carbon NMR signals using the numbering given on the structure. Additionally, present your data in table form including chemical shift, integration, coupling pattern, and coupling constants (where possible). For mass spectral data, justify key fragmentations (those which are starred*) by proposing fragment structures. 5 96337 03828 047734 739073 23444 14703 3 8 9 2...

  • The H-NMR spectrum of an unknown compound (formula CaHgO2) is shown below. Draw the structure of...

    The H-NMR spectrum of an unknown compound (formula CaHgO2) is shown below. Draw the structure of the unknown compound. Question 5 4 1 6 5 8 10 11 Ppm The 13C-NMR spectrum of an unknown compound (formula CgH180) is shown below. Its 1H-NMR spectrum only shows one singlet at 1.2 ppm. Draw the structure of this unknown compound. uestion 2 220 200 160 140 120 PPM 100 80 240 180 60 40 20 Create OscerSketch Answer 2 What would be...

  • Compound 21 is a liquid (boiling point 60" C) that has Z stereochemistry. The Mass, IR, and H NMR spectra, along with 1...

    Compound 21 is a liquid (boiling point 60" C) that has Z stereochemistry. The Mass, IR, and H NMR spectra, along with 13C NMR data, are given below. Elemental Analysis: C, 24.78; H, 208; contains a halogen Mass Spectrum 61 96 98 30 40 50 60 70 80 90 100 110 120 130 140 150 180 170 180 190 200 mVe Infrared Spectrum Wave Number, cm - 4000 3000 2500 1500 2000 1300 1200 1100 800 700 1000 900 ww...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT