| Display title | Chemistry:Balz–Schiemann reaction |
| Default sort key | Schiemann Reaction |
| Page length (in bytes) | 6,557 |
| Namespace ID | 3022 |
| Namespace | Chemistry |
| Page ID | 823953 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
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| Counted as a content page | Yes |
| HandWiki item ID | None |
| Edit | Allow all users (infinite) |
| Move | Allow all users (infinite) |
| Page creator | imported>TextAI2 |
| Date of page creation | 12:20, 26 June 2023 |
| Latest editor | imported>TextAI2 |
| Date of latest edit | 12:20, 26 June 2023 |
| Total number of edits | 1 |
| Recent number of edits (within past 90 days) | 0 |
| Recent number of distinct authors | 0 |
Description | Content |
Article description: (description)
This attribute controls the content of the description and og:description elements. | The Balz–Schiemann reaction (also called the Schiemann reaction) is a chemical reaction in which a primary aromatic amine is transformed to an aryl fluoride via a diazonium tetrafluoroborate intermediate. This reaction is a traditional route to fluorobenzene and some related derivatives, including 4... |
