For each of the compounds below tell how many signals you would expect the molecule to have in its normal, broadband decoupled 13C NMR spectra.
-Which of the following compounds would produce the most downfield signal in a 13C NMR spectrum? A
B
C
D
A) A
B) B
C) C
D) D
Correct Answer:
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Q3: For each of the compounds below tell
Q4: Predict the splitting patterns you would expect
Q5: Which of the following would not produce
Q6: For each of the compounds below tell
Q9: Nuclear magnetic resonance spectroscopy provides information about
Q10: For each of the compounds below tell
Q11: For each of the compounds below tell
Q13: For each of the compounds below tell
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Q60: Instructions: Refer to the structure of 3-methylbutan-2-one
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