Question

Which one of the following best represents the predicted approximate chemical shift and coupling for the hydrogen(s) indicate
0 0
Add a comment Improve this question Transcribed image text
Answer #1

2.10ppm singlet..

since the ch3 group is attatched to c=o group, there is no hydrogen group interaction , hence no splitting, giving rise to a singlet

Add a comment
Know the answer?
Add Answer to:
Which one of the following best represents the predicted approximate chemical shift and coupling for the...
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
  • Question 37 Which one of the following best represents the predicted approximate chemical shift and splitting...

    Question 37 Which one of the following best represents the predicted approximate chemical shift and splitting for the hydrogen(s) indicated with the arrow in the compound nicotine 500 om inget 5.00 pom doutlet Question 38 Which one of the following best represents the predicted approximate chemical shift and splitting for the hydrogen(s) indicated with the arrow? Co-CH₃ - 1.10 ppm, singlet 2.10 ppm, doublet 3.40 ppm, singlet 45 ppm, singlet 3.5 ppm, quartet

  • Question 23 What is the product, W, of the following reaction sequence? i. NaOEt niin ii....

    Question 23 What is the product, W, of the following reaction sequence? i. NaOEt niin ii. NaOtButyliv. NaOH v.H30* heat (-CO) W 1 equiv. 11.Br 1 equiv. HOC -COH HOC EtO2- o COH -CO EL Ι II III i COH IV V A. III B. C.IN D. V E. IV Question 24 Which one of the following best represents the predicted approximate chemical shift and coupling for the hydrogen(s) indicated with the arrow? A. 2.40 ppm, quartet B. 2.40 ppm,...

  • 50. For the following compound how many different signals would you see in the proton NMR?...

    50. For the following compound how many different signals would you see in the proton NMR? (Assume that you can see them all.) A) 4 B) 5 C) 6 D) 7 E) 8 . An organic compound absorbs strongly in the IR at 1687 em. Its 'H NMR spectrum consists of two signals, a singlet at 2.1 ppm and a multiplet centered at 7.1 ppm. Its mass spectrum shows significant peaks at m/z 120, m/z 105 and m/z 77. This...

  • 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...

  • Thank you!! 2. (5.5pts) Use your spectroscopy data table to identify the chemical shift range in...

    Thank you!! 2. (5.5pts) Use your spectroscopy data table to identify the chemical shift range in which each of the identified signals in the following molecule would be found in the H NMR spectrum 3. (7.5pts) Indicate the expected level of splitting in the signals for the protons indicated by the arrows. Use the appropriate symbol (ie s = singlet, da doublet, etc). Assume no splitting of/by NH and OH protons no les poques Chemical Shift 0.5-6 ppm 0.9-2 ppm...

  • For NMR Structure of following compounds: Why splitting is like this?Why chemical shifts are like this?So...

    For NMR Structure of following compounds: Why splitting is like this?Why chemical shifts are like this?So i have the answer of this question here.But i need detailed explanation. (a) Sketch the 'H NMR spectrum you would expect for the following compounds, showing the splitting patterns, chemical shifts and integration of each signal. Explain in detail. (40P) OH CI CH(CH3)2 4-isopropylphenol H3C OH 3-chloro-2-buten-1-ol 9.06 ОН 6.68 6.68 7.22 27.22 12.87 120 120 10 PPM Two CH3 groups appear as doublet...

  • 7. Which compound below best fits the following spectral data? 8. How many signals would you...

    7. Which compound below best fits the following spectral data? 8. How many signals would you expect to see in the broadband decoupled C^13 spectra of the following compounds? 9. If a proton gave an NMR signal at 3.2 ppm on a MHz NMR, what would the chemical shift be of this proton (in ppm) if the sample was run in 400 MHz NMR? 7. Which compound below best fits the following spectral data? (6 points) H-1 NMR 0.9 ppm...

  • please only answer if you are sure and be aware there is more then one part...

    please only answer if you are sure and be aware there is more then one part to the question. thanks Q7. NMR OF METHYL 4-HYDROXYBENZOATE The 'H NMR spectrum of methyl 4-hydroxybenzoate, recorded on a 300 MHz spectrometer in DMSO, is shown below. Use this spectrum for the subsequent analysis. You can zoom in to an area of the spectrum by click and dragging over the area you want. You can zoom out by double clicking anywhere on the spectrum...

  • Review Question 10.010 Explain why two liters of hydrogen gas and one liter of oxygen gas...

    Review Question 10.010 Explain why two liters of hydrogen gas and one liter of oxygen gas react to form two liters of water, when the pressures and temperatures are held constant. Since the pressures and temperatures are constant, the ratio of the volumes is equivalent to the stoichiometric ratio. The balanced chemical equation is (Include physical states in your answer and use smallest integer coefficients to balance the equation.): I ? Edit Edit liter(s) of oxygen will form liter(s) of...

  • Hi could you help me with this problem please? The following spectroscopic data were obtained for...

    Hi could you help me with this problem please? The following spectroscopic data were obtained for an organic compound: i. MS (relative abundance in parentheses): M+ = 86 ; signals at 29 (92) and 41 (100) among others ii. IR (cm-1): 3100 (weak sharp), 2970 (medium sharp), 2850 (medium), 1650 (weak sharp), 1100 (strong sharp) iii. H1 NMR :     Signal A at 4 ppm (3H, triplet),     Signal B at 3.53 ppm (2H quartet),     Signal C at 4.01...

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