Chapter 18: 24 P (page 708)
Draw the products of each reaction.
Chapter 18: 24 P (page 708)
Draw the products of each reaction.
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Get started for freeDraw all resonance structures for the carbocation formed by ortho attack of the electrophile on each starting material. Label any resonance structures that are especially stable or unstable.
Question: Devise a stepwise mechanism for the following reaction. The reaction does not take place by direct electrophilic aromatic substitution at C2 . (Hint: The mechanism begins with addition of an electrophile at C3.)
Question: Propose a structure of compound C (molecular formula ) consistent with the following data. C is partly responsible for the odor and flavor of raspberries. Compound C: IR absorption at 1717 cmโ1.
Draw the products of each reaction.
In Step [2] of Mechanism 18.1, loss of a proton to form the substitution product was drawn using one resonance structure only. Use curved arrows to show how the other two resonance structures can be converted to the substitution product (PhE) by removal of a proton with: B.
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