00:01
How would you synthesize the following compounds? so we have to prepare the following compounds.
00:16
So benzene we have.
00:17
This benzene is reacting with the first cs3 cl in the presence of cs3 in the presence of elcl3.
00:25
Then we are getting toluene.
00:27
Then we are getting toluene.
00:29
This tallowin is reacting with the hno3 h2x4.
00:34
This talluline is reacting with the hno3 h2s4.
00:40
So this region is producing an o2 as the electrophile this electrophile will attack on the paraposition because cs3 is the electron releasing group so cs3 here and no2 here now this compound is reacting with the br2 in the presence of the febr3 so this reagent is producing br plus as the electro file this br plus will attack on the orthoposition with respect to cs3 because cs3 is the electron releasing group.
01:22
And in the second structure, what we have? then in the second structure, we have c2h5, so3h.
01:39
C3, not c2h5, s3h, ch2, ch2, ch3.
02:19
How can you prepare this product? here we have s3h, here this.
02:42
Orthometapara...