@AvatarShiny well I'll tell you one thing, if you continue to use social media everyday, your real name will be out one day. If not today, then tomorrow. Very soon ;)
Nothing is hidden on the internet. Nothing at all.
@M.A.R. Actually not funny because I just discovered $2k of fraud on my card
@AvatarShiny No, that's actually bad. You will have a snap judgement, but you should hold off acting on that until you can judge the individual on their own merits
@Zhe I think the question is "How did you assume that the rate of the formation of the intermediate is proportional to the concentration of $\ce{[A]}$?"
The big issue here is that there is confusion between the observed rate law, which is not the same thing as the actual rate law.
For example, there are pseudo zero order reactions, but it is impossible for a reaction to be truly zero order (what is reacting then?).
Consider the following conver...
The Meerwein arylation is an organic reaction involving the addition of an aryl diazonium salt (ArN2X) to an electron-poor alkene usually supported by a metal salt. The reaction product is an alkylated arene compound. The reaction is named after Hans Meerwein, one of its inventors who first published it in 1939.
An electron-withdrawing group (EWG) on the alkene makes it electron deficient and although the reaction mechanism is unclear, involvement of an aryl radical is presumed after loss of nitrogen in the diazonium salt followed by a free radical addition. In the primary reaction product the...
@Rick "An electron-withdrawing group (EWG) on the alkene makes it electron deficient and although the reaction mechanism is unclear,[2] involvement of an aryl radical is presumed "