Chapter 18: 23 P (page 706)
Devise a synthesis of each compound from the indicated starting material.
Chapter 18: 23 P (page 706)
Devise a synthesis of each compound from the indicated starting material.
All the tools & learning materials you need for study success - in one app.
Get started for freeDraw the structure of A, an intermediate in the synthesis of the antipsychotic drug risperidone. Explain why three rings in risperidone are considered aromatic.
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.
Draw the products formed when each compound is treated with
Draw all products formed when m-chlorotoluene is treated with in
Question: Explain the reactivity and orientation effects observed in each heterocycle.
a. Pyridine is less reactive than benzene in electrophilic aromatic substitution and yields 3-substituted products.
b. Pyrrole is more reactive than benzene in electrophilic aromatic substitution and yields 2-substituted products.
What do you think about this solution?
We value your feedback to improve our textbook solutions.