Yes, chiral centers do not have to be carbon atoms. Any atom that is bonded to four different groups can be a chiral center.
To identify chiral centers in ring structures, look for carbon atoms that are bonded to four different groups. These carbon atoms are chiral centers and can create stereoisomers.
To determine chiral centers in a molecule, look for carbon atoms bonded to four different groups. These carbon atoms are chiral centers, meaning they have non-superimposable mirror images.
To determine the number of chiral centers in a molecule, one must identify carbon atoms that are bonded to four different groups. These carbon atoms are considered chiral centers because they have a non-superimposable mirror image. Counting the number of these carbon atoms in the molecule will give you the total number of chiral centers.
Chiral centers in a molecule can be identified by looking for carbon atoms that are bonded to four different groups. These carbon atoms are asymmetric and can create mirror image structures, making the molecule chiral.
To determine chiral centers in rings, look for carbon atoms with four different groups attached. If a carbon atom in the ring has this arrangement, it is a chiral center.
To identify chiral centers in ring structures, look for carbon atoms that are bonded to four different groups. These carbon atoms are chiral centers and can create stereoisomers.
To determine chiral centers in a molecule, look for carbon atoms bonded to four different groups. These carbon atoms are chiral centers, meaning they have non-superimposable mirror images.
To determine the number of chiral centers in a molecule, one must identify carbon atoms that are bonded to four different groups. These carbon atoms are considered chiral centers because they have a non-superimposable mirror image. Counting the number of these carbon atoms in the molecule will give you the total number of chiral centers.
Chiral centers in a molecule can be identified by looking for carbon atoms that are bonded to four different groups. These carbon atoms are asymmetric and can create mirror image structures, making the molecule chiral.
To determine chiral centers in rings, look for carbon atoms with four different groups attached. If a carbon atom in the ring has this arrangement, it is a chiral center.
Stereogenic centers in a molecule can be determined by identifying carbon atoms that are bonded to four different groups. These carbon atoms are called chiral centers and are the stereogenic centers in the molecule.
There are 5 chiral carbon atoms in norethynodred.
Psicose has four chiral carbon atoms, so it has four chirality centers.
I think glucose has 4 chiral centres four carbon atoms has four different compound/elements bonded to it.
There are two chiral carbon atoms present in 2,3,4-trichloropentane.
Glucose is a Chiral molecule having 4 chiral carbons.
Norepinephrine has one chiral center, which is the carbon atom bonded to the amine group.