Type your answer here... Alkene
This is a cis molecule.
This is a single bonded compound and cis-trans isomerism is only possible when fre rotation about a bond is restricted or a double bond or cycle is essential for existence of cis-trans isomers.
No, CH3-CHCH-Br cannot exhibit cis-trans isomerization because there is only one stereocenter in the molecule, located at the carbon bearing the bromine atom. In order for cis-trans isomerization to occur, there must be a carbon-carbon double bond with two different substituents on each carbon atom.
13-cis lycopene is more stable than 7-cis and 11-cis because it has a more extended conjugated system, making it less prone to isomerization and oxidation. The increased delocalization of electrons in 13-cis lycopene results in higher stability compared to 7-cis and 11-cis isomers.
The type of molecule that is an enzyme is a protein molecule.
Type your answer here... Alkene
Type your answer here... Alkene
Yes, cis-1,4-dichlorocyclohexane is a chiral molecule.
This is a cis molecule.
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.
The type of stereoisomer
2pentene
C8H16 does not specify the arrangement of atoms, so it is neither cis nor trans. The cis/trans notation is used to describe relative positions of substituents on a molecule, typically alkenes or cycloalkanes.
You think probable to cis-2-pentene.
In the chair conformation of a molecule, cis isomers have substituents on the same side of the ring, while trans isomers have substituents on opposite sides of the ring.
p-dichlorobenzene is nonpolar because the electronegativity of chlorine is similar to that of carbon, resulting in a symmetrical molecule. In cis-1,4-dichlorocyclohexane, the molecule is asymmetrical due to the arrangement of the chlorine atoms on the cyclohexane ring, leading to a net dipole moment and making it a polar molecule.
This is a single bonded compound and cis-trans isomerism is only possible when fre rotation about a bond is restricted or a double bond or cycle is essential for existence of cis-trans isomers.