Fumarate has four carbon atoms.
Nonane has 9 carbon atoms and the formula of C9H20
Decane has 10 carbon atoms and 22 hydrogen atoms in it.
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.
Methenolone, an anabolic steroid, has one chiral center at the carbon atom bound to the oxygen atom.
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'
Sucrose does not have any chiral centers because it is composed of two monosaccharides, glucose, and fructose, which are both not chiral in the specific form found in sucrose.
Norepinephrine has one chiral center, which is the carbon atom bonded to the amine group.
Aldoheptoses have seven carbon atoms and one chiral center, so they can have a maximum of 2^1 = 2 enantiomers.
There are two possible stereoisomers of 2,3-butanediol: meso and chiral forms. The meso form has an internal plane of symmetry, resulting in only one unique 3D structure. The chiral form, on the other hand, has two enantiomeric forms (mirror images) due to the presence of a chiral center at the carbon atoms.