-
I want to add one super fast addendum
-
to the video on Friedel-Crafts acylation.
-
In the last step of the mechanism,
-
I had this chlorine swipe the electron,
-
or essentially that electron that was with the aluminum.
-
It was given to the hydrogen proton.
-
So the hydrogen was nabbed away.
-
Its electron was allowed to go back into the benzene ring.
-
So the aluminum lost a chlorine.
-
This benzene ring lost a proton.
-
It was able to take back that electron.
-
And I forgot to draw the hydrogen and the chlorine.
-
So then that results in hydrogen chloride.
-
So you have the hydrogen proton bonded.
-
It took this electron from the aluminum.
-
And it is bonded to the chlorine.
-
I didn't want to forget that in that last step
-
of the Friedel-Crafts acylation.
-
We also get some hydrogen chloride.