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Grade: 12th pass
        
Birch reduction of Toulene gives
3 years ago

Answers : (8)

Sakshi
askIITians Faculty
652 Points
							496-793_hello.PNG
						
3 years ago
grenade
2056 Points
							
@ Sakshi the answer might be wrong bcoz here anti aromatic compound is formed
Plz aprve
3 years ago
grenade
2056 Points
							
Oops mistook
The answer is correct(Sakshi)
I forgot about the delocalisation of Tye double bond
3 years ago
Kartikey Sharma
19 Points
							
Delocalisation will be thee only when conjugation is there i.e double bonds are separated by a single bond so the second stucture is wrong.
If any mistake is on my side than pls show me the change from first structure into the other.
3 years ago
grenade
2056 Points
							
Yes because the anti aromatic is firmed when there is an complete delocalisation of electron
The answer given by Sakshi is correct pl. Check out and the answer is  non aromatic
 
Please approve
3 years ago
grenade
2056 Points
							
U are wrong I check my books completely
3 years ago
Kartikey Sharma
19 Points
							
I also know the answer is non aromatic but i was asking that in the above given equation the two structures given in the product how are they interconvertible into one another as to form  resonating structures you must have conjugation between the pi-pi electons.
3 years ago
Sakshi
askIITians Faculty
652 Points
							Hi..
The two structures mentioned in the above answer are not the interconvertable forms.
This actually depicts that on the reduction of toluene either the first structure or the second structure will be obtained. This is because there is delocalization in the benzene ring and hence either of the two compounds cam be formed.
It is just the representation which is different, both are actually the same compounds.
Hope this clears the doubt now..
Regards
3 years ago
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