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What is a stereogenic center?
Carbon atoms that have four nonidentical substituents are referred to as asymmetric carbon atoms. Asymmetric carbon are specific examples of a stereogenic center.In other words a carbon atom that has four different elements or compounds bonded to its a stereogenic center.
Is hydrogen a molecule?
Yes, hydrogen can exist as a molecule. In its diatomic form, hydrogen atoms can bond together to form a molecule called molecular hydrogen (H2).
How many atoms are there in a molecule of oygen?
There are 2 oxygen atoms in 1 molecule of oxygen.
How many carbon atoms are in the molecule ethanol?
There are four atoms of hydrogen in each molecule of methanol.
When a molecule has a positive end and a negative end it is called?
Molecules that have partially positive and negative regions are called polar molecules. Polarity results from an unequal attraction of electrons between the atoms that make up a molecule. The electrons are more drawn towards atoms with a higher electronegativity, thus making these atoms partially negative.
What is a stereogenic center?
Carbon atoms that have four nonidentical substituents are referred to as asymmetric carbon atoms. Asymmetric carbon are specific examples of a stereogenic center.In other words a carbon atom that has four different elements or compounds bonded to its a stereogenic center.
Which molecule is a stereoisomer of cis-2-pentene?
Trans-2 pentene is a stereoisomer of cis-2-pentene.
What is indicated of the prefix cis- and trans-?
The prefix cis- means "on the same side" and is used to indicate that two substituents are on the same side of a molecule. The prefix trans- means "across" and is used to indicate that two substituents are on opposite sides of a molecule.
Which molecule is a stereoisomer of trans-2-butene?
H3C-CH3 c=c H-H
What molecule is a stereoisomer of cis-2-pentene?
The stereoisomer of cis-2-pentene is trans-2-pentene. In cis-2-pentene, the two methyl groups (CH₃) are on the same side of the double bond, while in trans-2-pentene, they are on opposite sides. This difference in spatial arrangement gives rise to distinct physical and chemical properties between the two isomers.
What is indicated by the prefixes- and trans-?
The type of stereoisomer
What is the difference between epimers and anomers in carbohydrate chemistry?
Epimers are a type of stereoisomer that differ in the configuration of a single chiral center, while anomers are a type of epimer that specifically differ in the configuration of the anomeric carbon in a sugar molecule.
What is anomers?
it is a stereoisomer that differs in configuration at only one chiral center
Which prefix is used in the name of a stereoisomer to indicate that the functional groups are on the same side of the double bond?
The prefix "cis-" is used in the name of a stereoisomer to indicate that the functional groups are on the same side of the double bond.
What does erythorbic means?
Erythorbic is an acid. Erythorbic acid is a stereoisomer of ascorbic acid.
What is the name of the opposite stereoisomer of the molecules shown below?
To identify the opposite stereoisomer (also known as the enantiomer), I would need to see the specific molecular structures you are referring to. Generally, enantiomers are non-superimposable mirror images of each other, and they differ in their spatial arrangement around chiral centers. If you provide the structures or names of the molecules, I could help you determine the name of the opposite stereoisomer.
What is indicated by the prefixes cis- and trans?
The type of stereoisomer
