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- Jul 18, 2004
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I am reviewing TS and achiever right now.
Here are questions/ some parts of the questions I don't really understand...
1. H NMR on 1,4-dimethylbenzene
On achiever, it has 2 singlets. Ok, first singlet is due to methane groups.
So the second singlet is from benzene right?
I guess all the H's from benzene are equal in this case.
How about H NMR on 1-chloro 2methyl benzene?
Are all H's on benzene still same?
2. are they R/S configurations?
CH3 Br C00H
! ! !
Br-C-H F-C-CHO CH3-C-F
! ! !
COOH H NH3
Answer- R, S, S respectively.
Groups with bigger atomic # has higher priority.(assigned #)
so 1st one has priority in the order Br>COOH>CH3(going counterclockwise
but H is between CH3 and COOH(3rd priority) so
going clockwise..R?
I did the same method for the 2nd and 3rd ones, too.
But I got R, R, R configuration..
3) Is it possible to know Zn is gonna be reduced if given
the condition that Zn and Cu are in electrolysis?
I thought reduction potential for that.
Do u guys have any clues?
Thanks! 👍
Here are questions/ some parts of the questions I don't really understand...
1. H NMR on 1,4-dimethylbenzene
On achiever, it has 2 singlets. Ok, first singlet is due to methane groups.
So the second singlet is from benzene right?
I guess all the H's from benzene are equal in this case.
How about H NMR on 1-chloro 2methyl benzene?
Are all H's on benzene still same?
2. are they R/S configurations?
CH3 Br C00H
! ! !
Br-C-H F-C-CHO CH3-C-F
! ! !
COOH H NH3
Answer- R, S, S respectively.
Groups with bigger atomic # has higher priority.(assigned #)
so 1st one has priority in the order Br>COOH>CH3(going counterclockwise
but H is between CH3 and COOH(3rd priority) so
going clockwise..R?
I did the same method for the 2nd and 3rd ones, too.
But I got R, R, R configuration..
3) Is it possible to know Zn is gonna be reduced if given
the condition that Zn and Cu are in electrolysis?
I thought reduction potential for that.
Do u guys have any clues?
Thanks! 👍