The final product and the starting cyclohexanone are similar, and by looking at the structures you maywonder how you would be ableto tell that reaction actually occurred by comparingthe infrared spectra of the cyclohexanone and thefinal productwithout looking at the fingerprint region. however, the infrared spectra are above 1500 cm-1that they can readily be distinguished. it turns out that they are differentbecause of a perhaps unexpected structural feature of the final product, intramolecular hydrogen bonding. draw a structure of the final product that illustrates this intramolecular hydrogen bonding and how it arises. 8.(2pts.) provided is anir spectrumofthe cyclohexanone starting material. assign the peaks with frequencies greater than 1500 cm-1. remember that you must identify boththe functional groups andalso the specific bond vibration responsible for the peak or peaks in the ir spectrum. include allc-h bond vibrations. nooonoh3o oo2-acetylcyclohexanoneh cat. onh cyclohexanoneooh