Draw the structure of the compound identified by the following simulated 1H and 13C NMR spectra. The molecular formula of the co
mpound is C10H12O. (Blue numbers next to the lines in the 1H NMR spectra indicate the integration values.)
1 answer:
Answer: 4-allylanisole
Explanation: The doublets behind the 7 ppm belongs to the
para-substituted benzene ring. The three single-proton multi-plets around 5−6 ppm predicts that there has to be a single subsituted alkene group
A single plus a doublet around 3-4 ppm belongs to CH3 and CH2 Groups as they could be attached to the subsituted alkene group.
Moreover the interpretation of the NMR that there is no peak with a higher intensity for >180 ppm represents an absence of Carbonyl group.
The Predicted Number is attached from a chemical database along with their peaks information
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3) Halogenation of Cyclohexene (Electrophillic Addition Rxn) gives 1,2-dihalocyclohexane.
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