a) Draw the below structure and answer the following questions. CI CH2COCH2CH3 i. Identify the chemically equivalent protons in the structure. Explain your answer. ii. Mention how many peaks you would expect in the HNMR spectrum of the compound. Explain the position of each peak in the spectrum. iii. Mention what would be the splitting pattern of each peak with proper explanation. iv. Draw the HNMR spectrum of the compound. b) Explain why the delta/ ppm scale was introduced instead of Hz in NMR analysis with example.

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3.
a) Draw the below structure and answer the
following questions.
CI
CH2COCH2CH3
i. Identify the chemically equivalent protons in the
structure. Explain your answer.
ii. Mention how many peaks you would expect in
the HNMR spectrum of the compound. Explain
the position of each peak in the
spectrum.
iii. Mention what would be the splitting pattern of
each peak with proper explanation.
iv. Draw the HNMR spectrum of the compound.
b) Explain why the delta/ ppm scale was
introduced instead of Hz in NMR analysis with
example.
Transcribed Image Text:3. a) Draw the below structure and answer the following questions. CI CH2COCH2CH3 i. Identify the chemically equivalent protons in the structure. Explain your answer. ii. Mention how many peaks you would expect in the HNMR spectrum of the compound. Explain the position of each peak in the spectrum. iii. Mention what would be the splitting pattern of each peak with proper explanation. iv. Draw the HNMR spectrum of the compound. b) Explain why the delta/ ppm scale was introduced instead of Hz in NMR analysis with example.
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