SOLVED: Borneol has the hydroxyl group in the endo position while its diastereomer, isoborneol, has the hydroxyl group in the exo position. If you had performed this reaction using isoborneol, what differences, if any, would you expect in the product?

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using resonance theory to explain why the hydroxyl group ofphenol is an activating group and an ortho para director illustrate your explanation by showing the arenium ions formed when anilin 46583

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SOLVED: Alcohols, phenols, and thiols are classes of organic compounds containing a hydroxyl group (-OH), a phenol group (benzene ring with a hydroxyl group), or a thiol group (-SH), respectively, as the main functional group. What is the name of the compound shown here?

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