The protons associated with aromatic rings do not appear in the region we have b

Question

The protons associated with aromatic rings do not appear in the region we have been analyzing thus far. These protons appear further downfield (high ppm values) between 6.5 and 8 ppm depending on the presence of the substituents connected to the aromatic ring. Benzene is referred to as an aromatic hydrocarbon. The term "aromatic" has a long history and primarily refers to this very special class of compound. For our purposes, aromatic compounds contain the six member ring with alternating double bonds. It is absolutely essential to draw the double bonds in the ring. Without the three double bonds, this molecule is cyclohexane and the two molecules are radically different.

Explanation / Answer

Yes, the explanation is correct and all the hydrogens which are out of ring will face additional magnetic field and will appear at high ppm values 6.5-8 ppm. So that we can see a single peak between 6 and 8 ppm for 6H.

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