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- Phenylamine reacts with acids like hydrochloric acid in exactly the same way as any other amine. Despite the fact that the phenylamine is only a very weak base, with a strong acid like hydrochloric acid the reaction is completely straightforward. Phenylamine is only very slightly soluble in water, but dissolves freely in dilute hydrochloric acid.
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How does phenylamine react with nitrobenzene?
Jan 23, 2023 · Phenylamine reacts with acids like hydrochloric acid in exactly the same way as any other amine. Despite the fact that the phenylamine is only a very weak base, with a strong acid like hydrochloric acid the reaction is completely straightforward.
Phenylamine reacts with acids like hydrochloric acid in exactly the same way as any other amine. Despite the fact that the phenylamine is only a very weak base, with a strong acid like hydrochloric acid the reaction is completely straightforward.
Nitrobenzene is reduced to phenylammonium ions using a mixture of tin and concentrated hydrochloric acid. The mixture is heated under reflux in a boiling water bath for about half an hour. Under the acidic conditions, rather than getting phenylamine directly, you instead get phenylammonium ions formed.
Jan 23, 2023 · Nitrobenzene is reduced to phenylammonium ions using a mixture of tin and concentrated hydrochloric acid. The mixture is heated under reflux in a boiling water bath for about half an hour. Under the acidic conditions, rather than getting phenylamine directly, you instead get phenylammonium ions formed.
Step 2 - Nitrobenzene is reduced with hot tin (Sn) and concentrated hydrochloric acid (HCl) under reflux to form an acidic mixture that contains the organic product C 6 H 5 N + H 3; Step 3 - Sodium hydroxide (NaOH) is added to the acidic reaction mixture to form phenylamine; Step 4 - The phenylamine is separated from the reaction mixture by ...
This page looks at the reactions of amines as bases. Their basic properties include the reactions with dilute acids, water and copper (II) ions. It only deals with amines where the functional group is not attached directly to a benzene ring. Aromatic amines such as phenylamine (aniline) are much weaker bases than the amines discussed on this ...
Nitrobenzene is reduced with hot tin (Sn) and concentrated hydrochloric acid (HCl) under reflux to form an acidic mixture that contains the organic product C 6 H 5 N + H 3 Reduction of nitrobenzene. Refluxing nitrobenzene with hot tin and concentrated hydrochloric acid forms the phenylamine ion
