Display title | Chemistry:Hofmann elimination |
Default sort key | Hofmann Elimination |
Page length (in bytes) | 4,874 |
Namespace ID | 3022 |
Namespace | Chemistry |
Page ID | 822959 |
Page content language | en - English |
Page content model | wikitext |
Indexing by robots | Allowed |
Number of redirects to this page | 0 |
Counted as a content page | Yes |
Page image |  |
HandWiki item ID | None |
Edit | Allow all users (infinite) |
Move | Allow all users (infinite) |
Page creator | imported>Sherlock |
Date of page creation | 15:01, 26 June 2023 |
Latest editor | imported>Sherlock |
Date of latest edit | 15:01, 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. | Hofmann elimination is an elimination reaction of an amine to form alkenes. The least stable alkene (the one with the fewest substituents on the carbons of the double bond), called the Hofmann product, is formed. This tendency, known as the Hofmann alkene synthesis rule, is in contrast to usual elimination... |