Question

3. The HNMR of the product is shown below with the region of 7.5-9.0 ppm blown up for better view. Specifically, in terms of

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

(A) j-O내3 E) H H (C 0N D) (B) Now to Caubem 50 Moye 07gen onneced 0 CH3 Dikiening SngeePeak will appear tlose to (3-8-4 pm) a

Add a comment
Know the answer?
Add Answer to:
3. The HNMR of the product is shown below with the region of 7.5-9.0 ppm blown up for better view. Specifically, in ter...
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
  • 5.314 Whee 10.0 9.5 9.0 8.5 8.0 7.5 2.500 70 6.5 6.0 5.5 ppm 5.0 46...

    5.314 Whee 10.0 9.5 9.0 8.5 8.0 7.5 2.500 70 6.5 6.0 5.5 ppm 5.0 46 40 35 30 25 20 15 10 d. Shown below are the starting material propiophenone (1), and the product of alpha bromination (2), Determine how each compound could be easily identified by HNMR of the alkyl substituent by identifying the approximate chemical shift, integration, and splitting you would observe for the protons labeled in each compound. 4pts Proton Approx. shift, ppm Integ. Splitting: s,d,...

  • In the proton NMR for benzil, there are clearly some impurity peaks below 8 ppm. Although...

    In the proton NMR for benzil, there are clearly some impurity peaks below 8 ppm. Although we cannot assign these for certain, is it possible that these peaks come from unreacted benzoin? Why or why not? 8.0 8.3 7.5 8.2 NMR nuclei observed: H Solvent: CDCl3 NMR field strength: 400MHz 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 (ppm) f1 8.1 8.0 7.9 7.8 7.7 7.6 7.5 7.4 7.3 f1 (ppm) 11 10 12 13 14 2.0 1.5...

  • Fill out the tables below of the starting material and pure product by using the given...

    Fill out the tables below of the starting material and pure product by using the given NMR spectrums. Identify if the pure isomer of methyl nitrobenzoate as ortho, meta, or para. Complete the table below using your proton NMR spectrum of your starting material. Be sure to include all peaks. Note: The table is expandable. Use the structure below for the letter assignments in your table. Splitting Integration Assignment Peak (ppm) Other Notes -7.95 -7.92 0627 -787 785 7.30 751...

  • 3. Based on the integration of the peaks, what is the relative number of protons which...

    3. Based on the integration of the peaks, what is the relative number of protons which make up each signal? 4. Identify any common splitting patterns. (ie. Isopropyl, ethyl, etc) UN (43 MIL.) 10.02s, 1H), 7.716.J-2 Hz. ) 2.0 11.5 11.0 10.5 10.0 9.5 9.0 8.5 8.0 7.5 7.0 6.5 6.0 4.0 3.5 3.0 2.5 20 15 100.5 0.0 -0.5 -1.0 -1.5 -2. 5.5 5.0 4.5 fl (ppm)

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