Using one of the plots of IR transmission shown below, calculate the bond strength of the C-O double bond (HINT: treat the complicated molecule as a diatomic one, with everything other than the O lumped into a single “atom”). Explain why the frequencies could be different for the two different molecules shown.
Using one of the plots of IR transmission shown below, calculate the bond strength of the C-O double bond (HINT: treat the complicated molecule as a diatomic one, with everything other than the O lump...
Using one of the plots of IR transmission shown below, calculate the bond strength of the C-O double bond (HINT: treat the complicated molecule as a diatomic one, with everything other than the O lumped into a single “atom”). Explain why the frequencies could be different for the two different molecules shown. C-H fingerprint region 40 0 1709 1716 3500 3000 2000 1500 1000 1500 Wavenumber (cm Wavenumber (cm')
If you could help explain the chart above, that would be awesome. 4. Analyze the IR spectrum of your product, filling in the table below. You should utilize your course textbook (pp. 764-766), if you need assistance. Please note that the frequency given below should be exact (one number), not a range. Use the frequency of the center of the band at its strongest point. Then, on the spectrum itself, mark the characteristic bands at their strongest point with a...
3. (3 pts.) Shown below is the IR spectrum 2-acetylcyclohexanone (the structure is provided in the spectrum). 2- acetylcyclohexanone exists as an equilibrium mixture of diketone and two enol forms. Both the diketone and enol forms can be seen in the provide IR spectrum, although the 2 different enols cannot be distinguished. The IR spectra of both enols is essentially identical and so do not be concerned with distinguishing the enols, just assign peaks to a “generic" enol. On the...