Attached is the H NMR for an unknown aldehyde reacted with acetophenone (in an aldol reaction) The aldehyde is either p-anisaldehyde or p-tolualdehye   Using the 1H NMR spectrum, draw the structure of the compound and assign the various resonances to the hydrogen nuclei responsible for them.  Which peak(s) were most significant in helping you identify your compound? Give a brief explanation for how you identified your compound. Briefly explain why signal c gives complex splitting.

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
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Attached is the H NMR for an unknown aldehyde reacted with acetophenone (in an aldol reaction)

The aldehyde is either p-anisaldehyde or p-tolualdehye

 

  1. Using the 1H NMR spectrum, draw the structure of the compound and assign the various resonances to the hydrogen nuclei responsible for them. 
  2. Which peak(s) were most significant in helping you identify your compound? Give a brief explanation for how you identified your compound.
  3. Briefly explain why signal c gives complex splitting.

 

Aldol with aldehyde C and acetophenone (performed in CDCI3 at 400 MHz)
d (1)
(2)(2),
g
1 21
3
8.
7
5
PPM
4
2
Transcribed Image Text:Aldol with aldehyde C and acetophenone (performed in CDCI3 at 400 MHz) d (1) (2)(2), g 1 21 3 8. 7 5 PPM 4 2
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