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0 votes
0 answers
31 views

Improve the leaving capability of a leaving group (F-) with electron density donating groups (EDP) in close proximity (neighboring group effect)?

I have a situation in which I want to hydrolyze a phosphonic acid halide under basic conditions. In my specific case, the halide is a fluorine substituent. Other halides like chlorine and bromine are ...
raptorlane's user avatar
0 votes
1 answer
403 views

What drives double displacement reactions?

I have two questions: I understand that in a displacement reaction the more reactive element displace the less reactive element. But why? In the reaction with Zinc and Copper Sulfate, we form Copper ...
Quin Gardiner Bax's user avatar
-1 votes
2 answers
222 views

Can a weak acid react to give a stronger acid? [closed]

I was trying to understand why $\ce{AgCl}$ does not dissolve in $\ce{HNO3}$ and the reaction I could think of was something like this: $$\ce{AgCl + HNO3->AgNO3 + HCl}$$ I could not understand why ...
Mia's user avatar
  • 11
3 votes
1 answer
786 views

Why can't Grignard reagents react like Organolithium does (with acids)?

I'd read yesterday that Grignard reagents can't give ketones on reaction with carboxylic acids. It is because of the fact that Grignard reagent is a "super-base", and it will deprotonate the ...
Rahul Verma's user avatar
  • 3,071