Chapter 18: 40 P (page 722)
Draw the products of each reaction.
Short Answer
a.
Chapter 18: 40 P (page 722)
Draw the products of each reaction.
a.
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Question: Draw a stepwise, detailed mechanism for the dienone–phenol rearrangement, a reaction that forms alkyl-substituted phenols from cyclohexadienones.
Draw the products of each reaction.
Question: Carboxylic acid X is an intermediate in the multistep synthesis of proparacaine, a local anesthetic. Devise a synthesis of X from phenol and any needed organic or inorganic reagents.
Which substituents have an electron-withdrawing and which have an electron-donating inductive effect
a
b
c
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