3
msp
·2009-02-16 07:43:55
have i given the correct reason or i blabbered
1
voldy
·2009-02-14 07:48:37
why do you ppl bring in magner weermein here ?? It's not possible . the secondary hydrogen alone reacts.
no rearrangement , according to me , forgive me if I'm wrong
If you disagree , then give some proof. I'd like to know of some source which says that this thing is possible . thanks in advance.
3
msp
·2009-02-14 08:07:53
@sky
free radicals are very very reactive , they react readily with another free radical to get a product and so they didnt have enuf time to get rearranged.
1
chinmay
·2009-02-14 08:16:44
does free radical undergo rearrangement like carbocations??
1
vector
·2009-02-16 05:36:56
free radical do not undergo rearrangement never
1
skygirl
·2009-02-16 07:32:02
who / what is this magner weermein ?? [seeing it first tym]
1
chinmay
·2009-02-16 07:35:40
Then how is this product possible??
1
skygirl
·2009-02-16 07:41:02
YUP! I WAS WRONG IN MY PREVIOUS POST...
THANX TO ALL OF YOU FOR CORRECTING ME!!
I READ IT JUS NOW IN MORRISON ...
REARRANGEMENT NOT POSSIBLE IN FREE-RADICALS ...
TX AGAIN :)
3
msp
·2009-02-16 07:43:29
sky wat is the reason given in the buk
1
skygirl
·2009-02-16 07:50:39
i dun think u blabbered...
reason not given .. [not given in the part i read]
only evidence given ....
3
msp
·2009-02-16 07:54:13
btw sky have u completed morrison & boyd
1
voldy
·2009-02-16 07:57:10
http://en.wikipedia.org/wiki/Wagner-Meerwein_rearrangement
1
skygirl
·2009-02-16 08:00:50
kk srinath :)
@sankara ... no i havent completed ... but read almost ...
missed many things as well ... like this one... its an imp thing i overlooked :( ... tx u guys :)
3
msp
·2009-02-16 08:02:51
sri i dunno wat u want to say abt the rearrangement da
1
voldy
·2009-02-16 08:04:38
I've not said anything just gave link.
1
voldy
·2009-02-14 03:28:53
wagner meerwein is only for carbocations. not free radicals.
21
tapanmast Vora
·2009-02-14 02:59:44
hi dude,
i guess one of the primary H must get replaced as photochemical bromiantion occurs by free radical if i'm not wrong....
am i on the rite track then i'll think wether its the one on 1st carb or the 4th.....
else [2]
21
tapanmast Vora
·2009-02-14 03:00:41
hey mathie : y methyl shift?? [7]
24
eureka123
·2009-02-14 03:01:49
yup mathematics u r correct..........can u give the mechanism........plzzzz[1]
39
Dr.House
·2009-02-14 03:07:20
thanks dude.
nothing great, bromine is highly regioselective. use that fact and u will get it.
39
Dr.House
·2009-02-14 03:07:49
@tapanmast : wagner meerwein rearrangement
1
voldy
·2009-02-14 03:09:58
believe me , it's not possible . even if you think out of the box. I'm quite sure on this. onyl secondary hydrogen will be substituted.
24
eureka123
·2009-02-14 03:09:59
actually i am confused about reactivity of Bromine.......I know its higly selective....but not in detail..........can anyone of u ,plz explain any arbitrary reaction in detail????plzzzzzz[1]
21
tapanmast Vora
·2009-02-14 03:25:18
yo mathie rite [4] ......
i forgot dat again???
ur name shud be CHEMISTRIAN!!!! LOL....
39
Dr.House
·2009-02-14 02:59:28
2-bromo 2,3 dimethyl butane
3
msp
·2009-02-14 04:53:19
the selectivity factor for BROMINATION
P: S: T
1: 82:1600
WHERE P IS PRIMARY HYDROGEN
S IS SECONDARY HYDROGEN
T IS TERITARY HYDROGEN