Question:

For the following compound
compound-signals expected in the 1H NMR spectrum
the number of signals expected in the 1H NMR spectrum is _________.

Updated On: Jan 11, 2025
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Correct Answer: 2

Solution and Explanation

In the given compound, we have two distinct types of protons:

  1. The two methoxy groups (−OCH3) each have identical protons, and they are chemically equivalent.
  2. The protons on the benzene ring are all equivalent because of the symmetry of the structure (with methoxy groups at the ortho positions relative to each other).

Therefore, the 1H NMR spectrum will exhibit two signals:

  1. A signal for the methoxy protons (OCH3).
  2. A signal for the aromatic protons on the benzene ring.

Thus, the correct number of signals is 2

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