The O of the hydroxyl of methyl salicylate is involved is resonance with the ring. Use carefully-drawn resonance structures to explain which of the carbons of the ring become cationic or anionic. Then state what effect this resonance is expected to have on the ¹H-NMR chemical shift of the H attached to those carbons.

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Chapter1: Chemical Foundations
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The O of the hydroxyl of methyl salicylate is involved is resonance with the ring.
Use carefully-drawn resonance structures to explain which of the carbons of the
ring become cationic or anionic. Then state what effect this resonance is expected
to have on the ¹H-NMR chemical shift of the H attached to those carbons.
Transcribed Image Text:The O of the hydroxyl of methyl salicylate is involved is resonance with the ring. Use carefully-drawn resonance structures to explain which of the carbons of the ring become cationic or anionic. Then state what effect this resonance is expected to have on the ¹H-NMR chemical shift of the H attached to those carbons.
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