aldo pentose contain 3 chairal carbon
four carbon atoms
Nonane has 9 carbon atoms and the formula of C9H20
Decane has 10 carbon atoms and 22 hydrogen atoms.
Malate has four carbon atoms.
There are approximately 163,163 atoms of carbon in 0.020 g of carbon.
There are two chiral carbon atoms present in 2,3,4-trichloropentane.
There are 5 chiral carbon atoms in norethynodred.
The structure appears to have 8 chiral carbons.
Psicose has four chiral carbon atoms, so it has four chirality centers.
Heroin has one chiral carbon.
Butaclamol has one chiral carbon, which means it can exist as two enantiomers.
A carbon atom needs to have 4 different substituents bonded to it in order for it to be chiral. This is known as a chiral carbon or a stereocenter.
From its name:(4S,6S,12aS)-4-(dimethylamino)- 3,6,10,12,12a-pentahydroxy- 6-methyl-1,11-dioxo-1,4,4a,5,5a,6,11,12a- octahydrotetracene-2-carboxamideyou can learn that there are: three chiral C-atoms,all in S-configuration, located at 4S(dimethylamino) and 6S(hydroxy) and 12aS(hydroxy) on the 'tetracene rings'
I think glucose has 4 chiral centres four carbon atoms has four different compound/elements bonded to it.
Aldoheptoses have seven carbon atoms and one chiral center, so they can have a maximum of 2^1 = 2 enantiomers.
Norepinephrine has one chiral center, which is the carbon atom bonded to the amine group.
Lipitor, also known as atorvastatin, has one chiral carbon in its molecular structure. This chiral center contributes to the drug's stereochemistry, which is important for its biological activity. The presence of this chiral carbon allows for the existence of enantiomers, but Lipitor is typically administered as a single enantiomer.