Chapter 18: 18 P (page 697)
Rank the following compounds in order of increasing reactivity in electrophilic aromatic substitution.
Chapter 18: 18 P (page 697)
Rank the following compounds in order of increasing reactivity in electrophilic aromatic substitution.
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Get started for freeExplain why each of the following reactions will not form the given product. Then, design a synthesis of A from benzene and B from phenol .
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.
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 cm–1.
Draw all resonance structures for each compound and use the resonance structures to determine if the substituent has an electron-donating or electron-withdrawing resonance effect.
Draw the products formed when A and B are treated with each of the following reagents:
(a),; (b)l3; (c)
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