Talk:Diazonium compound

Unless there are any objections, I will merge diazonium and diazo into this article in a week or so. Edgar181 13:58, 5 December 2005 (UTC)[reply]

Done. Edgar181 19:55, 9 December 2005 (UTC)[reply]

Request

A mechanism of its formation from amine and HNO₂ would be great! Aaadddaaammm 03:53, 1 November 2006 (UTC)[reply]

Update required

On the nanotechnology section. Electrografting to chromium has been reported which is to the left of iron in the periodic table. Hinge, Pedersen, New Journal of Chemistry, 33, 2009, 2405 —Preceding unsigned comment added by 137.222.44.218 (talk) 09:04, 22 October 2010 (UTC)[reply]

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Replacement by hydrogen

Sodium stannite = Sodium stannate(IV) is hardly a reducing agent. There may be a sodium stannate(II) which should be expected to have reducing properties.150.227.15.253 (talk) 10:02, 7 February 2020 (UTC)[reply]

Overvew of "General properties ..."

Take a look at the section: "General properties and reactivity"

Hefty section diazomethane is tangential because diazomethane is not a diazonium compound
"In terms of reactivity, the chemistry of diazonium salts is dominated by their propensity to dediazotize..."... the dominant and useful chem is probably diazo coupling, hands down.
Where is the X-ray data?
"Arenediazonium salts are exceptionally versatile reagents for chemical synthesis..." seems like an overstatement. Yes, they do a lot of reactions, but they are seldom in my experience.

--Smokefoot (talk) 15:25, 16 February 2022 (UTC)[reply]