|
[VIEWED 9159
TIMES]
|
SAVE! for ease of future access.
|
|
|
|
blackheaven123
Please log in to subscribe to blackheaven123's postings.
Posted on 01-19-12 12:19
AM
Reply
[Subscribe]
|
Login in to Rate this Post:
0 
? 
|
| |
how many seterocenters are there in cortisone ? please show in diagram .
|
| |
|
|
|
|
jantare1
Please log in to subscribe to jantare1's postings.
Posted on 01-19-12 3:24
AM [Snapshot: 76]
Reply
[Subscribe]
|
| Login in to Rate this Post:
1
?
Liked by
|
| |
6 stereocenters total, labeled 1 through 6; assign R/S configuration yourself if needed
|
| |
|
|
bhustigre
Please log in to subscribe to bhustigre's postings.
Posted on 01-19-12 11:27
AM [Snapshot: 187]
Reply
[Subscribe]
|
| Login in to Rate this Post:
0
?
|
| |
Jantarei is right..there are 6 stereocenter..5 located in ring juncture, and 1 in the end ring.
|
| |
|
|
NALAPANI
Please log in to subscribe to NALAPANI's postings.
Posted on 01-19-12 10:55
PM [Snapshot: 334]
Reply
[Subscribe]
|
| Login in to Rate this Post:
0
?
|
| |
You can't assign configuration of this molecule unless you know the bonds that are coming towards you and going away from you. However, if you assume the least priority group points away from you this molecule has following configurations
1S, 2S 3R, 4S, 5S, 6S
|
| |
|
|
jhapaliketo
Please log in to subscribe to jhapaliketo's postings.
Posted on 01-20-12 6:19
AM [Snapshot: 423]
Reply
[Subscribe]
|
| Login in to Rate this Post:
0
?
|
| |
hate this chemistry...nearly failed in chemistry in 12..
|
| |
|
|
north pole
Please log in to subscribe to north pole's postings.
Posted on 01-20-12 1:07
PM [Snapshot: 483]
Reply
[Subscribe]
|
| Login in to Rate this Post:
0
?
|
| |
O-chem sucks when it mixes up stereochemistry and synthesis together alongwith all functional groups.
|
| |
.png)
