13
8
3
I think glucose has 4 chiral centres four carbon atoms has four different compound/elements bonded to it.
fifteen.
Aldotetroses have 2^n stereoisomers, where n is the number of chiral centers. In the case of an aldotetrose, with 4 chiral centers, there can exist 2^4 = 16 stereoisomers.
Five. The two connected by wedges to the nitrogen, the two with wedged hydrogens, and the one with the hashed hydroxide.
3
There are 5 chiral carbon atoms in norethynodred.
I think glucose has 4 chiral centres four carbon atoms has four different compound/elements bonded to it.
fifteen.
Psicose has four chiral carbon atoms, so it has four chirality centers.
Isoleucine and Threonine
3
No it doesnt have any....
For a molecule with n chiral centers, there are a possible 2^n isomers that can be formed.
Aldotetroses have 2^n stereoisomers, where n is the number of chiral centers. In the case of an aldotetrose, with 4 chiral centers, there can exist 2^4 = 16 stereoisomers.
For a molecule with n chiral centers, there are a possible 2^n isomers that can be formed.
There is only 1 center - 1 chiral carbon and hence two optically active isomers.