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By definition, an asymmetric carbon atom is one that is bonded to four different types of atoms or groups, hence, only one can be a hydrogen atom. If there were two hydrogen atoms you would not have four different kinds of atoms.

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Can you identify the asymmetric carbon in this molecule?

Yes, the asymmetric carbon in a molecule is a carbon atom that is bonded to four different groups or atoms.


What is diastereomers?

Diastereomers are only possible if a molecule has at least two asymmetric carbon atoms (a carbon attached to four different groups or atoms) so alkenes don't have these.


Is chiral carbon and asymmetric carbon is one and the same thing or different?

Chiral carbon and asymmetric carbon are the same thing. They both refer to a carbon atom in a molecule that is bonded to four different atoms or groups, resulting in non-superposable mirror images known as enantiomers.


What is definition chirality?

A carbon atom attached to four different groups through sigma bonds is an asymmetric carbon or chiral carbon, this phenomenon is CHIRALITY, it is a basic centre for existing of Enantiomers the stereo isomers.


What is true of an asymmetric carbon?

Every asymmetric carbon (also known as chiral carbon) atom has for different groups attached to it. Those molecules have no planes of symmetry or axes of symmetry with respect to chiral carbon atoms.


Can a asymmetric carbon atom create geometric isomers?

Yes, an asymmetric carbon atom (chiral center) can create geometric isomers if there are two different groups attached to it that cannot rotate freely around the bond connecting them. This leads to the formation of cis-trans isomers where the spatial arrangement of the groups differs.


How do you identify the asymmetric carbon in a molecule?

it's the one that says asymmetric on it it's in 10 pt times new roman


Is eugenol chiral?

Eugenol is not chiral because it contains no assymmetric carbons. (carbons with 4 different groups attached to it)


Why 2NDand 3RDcarbon in galactose is asymmetric?

The 2nd and 3rd carbon in galactose are asymmetric because they are attached to four different groups or atoms, making them chiral centers. This asymmetry at these carbons gives rise to different stereoisomers of galactose.


Why is glycine not optically active?

A optically active compound should have atleast one carbon atom attached to four different groups. glycine is not active because it has carbon atom attached to 2 hydrogen atoms , 1 amino group and 1 carboxylic group


What is a carbon atom to which four different atoms or groups are attached?

A carbon atom with four different atoms or groups attached is called a chiral carbon atom. It is also known as a stereocenter and gives rise to optical isomerism in molecules.


How can one identify chirality centers in a molecule?

Chirality 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 give the molecule its chirality.