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In a molecule, the equatorial position is generally more stable than the axial position.

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5mo ago

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Why is the most stable conformational isomer of cis-1-bromo-2-chlorocyclohexane bromine equatorial and chlorine axial instead of bromine axial and chlorine equatorial?

The most stable conformation has the larger bromine atom in the equatorial position to reduce steric hindrance caused by its size. Placing the smaller chlorine atom in the axial position minimizes the overall energy of the molecule due to the difference in size between bromine and chlorine. This arrangement follows the principles of minimizing steric hindrance and maximizing stability.


Which conformation, axial or equatorial, is more stable in a cyclohexane chair conformation?

The equatorial conformation is more stable in a cyclohexane chair conformation.


Why polar groups prefer psi axial position than equatorial?

Polar groups prefer the axial position in cyclohexane because it minimizes steric hindrance with neighboring atoms, allowing for better overlap of orbitals and stabilizing the molecule. In the axial position, the polar group experiences less repulsion from other groups compared to being in the equatorial position, which leads to a more energetically favorable conformation.


Which orientation, equatorial or axial, is more stable in terms of energy for a substituent in a cyclohexane chair conformation?

The equatorial orientation is more stable in terms of energy for a substituent in a cyclohexane chair conformation.


Why is the equatorial region more stable than the axial region?

The equatorial region is more stable than the axial region because it receives more consistent sunlight and heat throughout the year, leading to a more balanced climate and fewer extreme temperature fluctuations.


What is the significance of the boat conformation in terms of the positioning of axial and equatorial substituents in cyclohexane?

The boat conformation of cyclohexane is significant because it allows for the positioning of axial and equatorial substituents in a way that minimizes steric hindrance. Axial substituents are positioned vertically, while equatorial substituents are positioned horizontally, reducing the strain on the molecule and increasing stability.


What is the most stable confirmation of cyclohexane?

The most stable conformation of cyclohexane is the chair conformation. In this conformation, all carbon atoms are in a staggered position and there is minimal steric hindrance between the hydrogen atoms. This results in the lowest energy state for the molecule.


Which is more stable alpha-fructose of beta-fructose?

Beta is more stable. It is in the equatorial position. When glucose is in monomeric form this does not matter much but when polymerized. Alpha produces starch (OH Down) and Beta produces cellulose (OH UP).


What type of molecular structure does XeO2F2 have?

The XeO2F2 molecule has a seesaw structure.There is a set of unpaired electrons on the equatorial position not occupied by the two Oxygen atoms. The Fluorine atoms take up the axial positions on either side of the Xenon central atom


What is an equatorial atom?

An equatorial atom is an atom in a molecule that is positioned around the equator of a molecular structure, typically in a trigonal bipyramidal or octahedral geometry. These atoms are usually bulkier and experience less steric hindrance compared to axial atoms in the same molecule.


Why axial bonds are larger than equatorial bonds?

axial bonds are longer than equatorial bonds becz axial bond contain very less "s" character as compare to equatorial bond, hence probability of finding it near nucleus is less hence force of attraction by nucleus is less as compare to to equatorial bonds


Why axial bonds are longer than equatoria bonds in PF5 bonds in space geometry?

The axial bond is 158 pm and the equatorial is 152 pm. One explanation is that the hybridisation of the equatorial bonds is sp2 and the hybridisation of the equatorial is pd, the greater s character of the equatorial making the bond shorter. (taken from text book Inorganic chemistry by House) I know of no theretical study that backs this up. Most text books duck this ,e.g Greenwood and Wiberg.