hNMR question

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in achiever. there is a quesion about p-xylene. can someone explain why only 2 singlets would show up?
thanks
 
in achiever. there is a quesion about p-xylene. can someone explain why only 2 singlets would show up?
thanks

It is a symmetric molecular only have two kind of equivalent hydrogen. 6 hydrogen(singlet) on methyl group and 4 on benzene(doublet).

m-xylene will have 4 peak (6-H on methyl, one between two methyl and one opposite to it, and the rest two, which give out singlet, singlet, triplet and doublet respectively.)


and o-xylene will have 3 peak (6-H on methyl, two near methyl groups and two further away from methyl groups, Which give out singlet, doublet, triplet respectively)

Correct me.
 
After looking up how p-xylene looked like I could undrstand.

Hausee, you are correct.

Well, are we expected to know all the special names like that?

Why couldn't they just say p-toluene?
 
I guess so. I remember I saw them somewhere in the old ADA test. They just want to show off you know. :S



After looking up how p-xylene looked like I could undrstand.

Hausee, you are correct.

Well, are we expected to know all the special names like that?

Why couldn't they just say p-toluene?
 
does anyone know a resource that contains all the common names that we should know for DAT? 🙁
 
It is a symmetric molecular only have two kind of equivalent hydrogen. 6 hydrogen(singlet) on methyl group and 4 on benzene(doublet).

m-xylene will have 4 peak (6-H on methyl, one between two methyl and one opposite to it, and the rest two, which give out singlet, singlet, triplet and doublet respectively.)


and o-xylene will have 3 peak (6-H on methyl, two near methyl groups and two further away from methyl groups, Which give out singlet, doublet, triplet respectively)

Correct me.



Then for m-xylene, isn't there a plane of symmetry like in p-xylene?
so wouldn't it be less than 4?
 
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