answersLogoWhite

0


Want this question answered?

Be notified when an answer is posted

Add your answer:

Earn +20 pts
Q: Why terahedral complexes do not show geometrical isomerism?
Write your answer...
Submit
Still have questions?
magnify glass
imp
Related questions

Why does a tetrahedral complex of the type MA2B2 not show geometrical isomerism?

For Geometrical isomerism the free rotation about the bonds should be restricted so a double bonded or cyclic compound may show the geometrical isomerism.


How do alkenes show geometric isomerism?

all the non terminal straight chain alkenes show the geometrical isomerism..


Why don't alkanes have geometric isomers?

Alkynes always form a triple bond. This being so, essentially, all you have are the two carbon molecules and the triple bond! No matter what way your turn it, or how you look at it, even if in a mirror (ie. optical isomerism) you will always have the same looking molecule while to have a geometrical isomer cis or trans form should be there. gen equation for a compound to be a geometrica isomer: 1.YXC = CXY 2.YXC = CXZ


Why 2-butene show geometric isomerism while 1-butene does not?

2-butene show geomatric isomerism because each double bond carbon atom has two different group


Dmg is tri or bidentate ligand?

it is a bi dentate ligand although it is an unsymmetrical ligand but its square planar complex can not show geometrical isomerism becoz of intra molecular H - bonding See also the structure of [Ni(dmg)2] i.e nickel dmg complex


Why elctrovalent compound does not show the isomerism while covalent compound show isomerism?

Nt sure I agree with the question. Consider the octahedral polyatomic ion Co(NH3)4Cl2+ this has trans and cis isomers (chlorines opposite each other at 180 0 or next to each other at 90 0). Generelly isomerism is rare in electrovalent compounds. One interesting example is the optical isomerism of ammonium sodium tartrate discovered by Pasteur.


What are the isomers of 1-chloro-1-fluorocyclopropane?

This is only one compound and does not show isomerism.


Does 3-octene show cis-trans isomerism?

Yes, 3-octene can exhibit cis-trans isomerism due to the presence of a carbon-carbon double bond. In the cis isomer, the two substituent groups are on the same side of the double bond, while in the trans isomer they are on opposite sides.


Why do alkenes show cis-trans isomerism?

Alkenes show cis-trans isomerism due to the restricted rotation around the carbon-carbon double bond. In cis isomers, the similar substituents are on the same side of the double bond, while in trans isomers, they are on opposite sides. This difference in spatial arrangement affects the physical and chemical properties of the isomers.


Could you show geometrical shapes?

what is netting?and netting in geimetrical shapes


Which amino acid does not show any optical isomerism?

Glycine because it is not chiral :)


What is the difference between positional isomerism and functional isomerism?

Positional isomerism refers to compounds with the same molecular formula but differing in the position of functional groups or substituents on the carbon skeleton, while functional isomerism involves compounds with the same molecular formula but differing in the functional groups present. In other words, positional isomers have the same functional groups but at different locations, whereas functional isomers have different functional groups altogether.