Question

Order the hydrogens for each molecule in the order you would expect to observe the peaks...

  1. Order the hydrogens for each molecule in the order you would expect to observe the peaks (upfield/downfield) for 3-methylbutylacetate, 3-methylbutanal, 3-methyl-1-butanol.
  2. Report the peaks as you see them for the proton NMR using the tables below:
  3. Compound:

    Peak

    shift

    mulitplicity

    Assignment

    Compound:

    Peak

    shift

    mulitplicity

    Assignment

    Compound:

    Peak

    shift

    mulitplicity

    Assignment

  4. Look at the 13C-NMR and list the peaks and assign them to the carbons in each.
  5. What similarities did you notice with the NMR peaks in the three compounds?
  1. NMR is a fantastic way for us to discern the structure of an unknown compound. Why do you think NMR might be more affective in this pursuit than IR?
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Answer #1

This 3 molecule show different peak in 1 H nmr ani IR vaule due to in 3 molecule having different functional group.

1st molecule having ester

2nd molecule having aldehyde.

3rd molecule having alcohol

This 3 functional group show 3 different IR and NMR vaule.. This are shown below, NMR o 3-methyl butyl Acetate IR- Ester group 17 sout d OL e 14 NMR a 64 (d) Nios (m) ~p.gr (b 14 24 29 ۱۰۸ بی (۹) 2 CH3 group

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