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- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/24%3A_Amines_and_Heterocycles/24.08%3A_Reactions_of_ArylaminesTo absorb all of it, you should use the three subsections indicated in the reading: electrophilic aromatic substitution and overreaction of aniline (Objectives 1 and 2), the preparation of diazonium s...To absorb all of it, you should use the three subsections indicated in the reading: electrophilic aromatic substitution and overreaction of aniline (Objectives 1 and 2), the preparation of diazonium salts and the Sandmeyer reaction (Objectives 3 and 4), and diazonium coupling reactions (Objective 5).
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(OpenStax)/24%3A_Amines_and_Heterocycles/24.08%3A_Reactions_of_ArylaminesThis section focuses on the unique reactions of arylamines, highlighting their reactivity compared to aliphatic amines. It discusses electrophilic aromatic substitution reactions, where arylamines can...This section focuses on the unique reactions of arylamines, highlighting their reactivity compared to aliphatic amines. It discusses electrophilic aromatic substitution reactions, where arylamines can act as nucleophiles, and their ability to form diazonium salts. The section also notes that the presence of the amino group can influence the reactivity of the aromatic ring, impacting various chemical transformations.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_III_(Morsch_et_al.)/24%3A_Amines_and_Heterocycles/24.08%3A_Reactions_of_ArylaminesTo absorb all of it, you should use the three subsections indicated in the reading: electrophilic aromatic substitution and overreaction of aniline (Objectives 1 and 2), the preparation of diazonium s...To absorb all of it, you should use the three subsections indicated in the reading: electrophilic aromatic substitution and overreaction of aniline (Objectives 1 and 2), the preparation of diazonium salts and the Sandmeyer reaction (Objectives 3 and 4), and diazonium coupling reactions (Objective 5).
- https://chem.libretexts.org/Courses/can/CHEM_232_-_Organic_Chemistry_II_(Puenzo)/10%3A_Amines_and_Heterocycles/10.09%3A_Reactions_of_ArylaminesTo absorb all of it, you should use the three subsections indicated in the reading: electrophilic aromatic substitution and overreaction of aniline (Objectives 1 and 2), the preparation of diazonium s...To absorb all of it, you should use the three subsections indicated in the reading: electrophilic aromatic substitution and overreaction of aniline (Objectives 1 and 2), the preparation of diazonium salts and the Sandmeyer reaction (Objectives 3 and 4), and diazonium coupling reactions (Objective 5).
- https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/24%3A_Amines_and_Heterocycles/24.09%3A_Reactions_of_ArylaminesTo absorb all of it, you should use the three subsections indicated in the reading: electrophilic aromatic substitution and overreaction of aniline (Objectives 1 and 2), the preparation of diazonium s...To absorb all of it, you should use the three subsections indicated in the reading: electrophilic aromatic substitution and overreaction of aniline (Objectives 1 and 2), the preparation of diazonium salts and the Sandmeyer reaction (Objectives 3 and 4), and diazonium coupling reactions (Objective 5).
- https://chem.libretexts.org/Workbench/LCDS_Organic_Chemistry_OER_Textbook_-_Todd_Trout/24%3A_Amines_and_Heterocycles/24.09%3A_Reactions_of_ArylaminesA phenol is prepared by reaction of the arenediazonium salt with copper(I) oxide in an aqueous solution of copper(II) nitrate, a reaction that is especially useful because few other general methods ex...A phenol is prepared by reaction of the arenediazonium salt with copper(I) oxide in an aqueous solution of copper(II) nitrate, a reaction that is especially useful because few other general methods exist for introducing an –OH group onto an aromatic ring.
