Gauche Eclipsed And Staggered Conformation. Organic chemistry newman and fischer conformational. This is the least stable conformation due to the steric strain caused by the proximity of the me groups and the torsional strain of the eclipsed bonds.
Usually, each conformer is also interconverted to the same forms by. Organic chemistry newman and fischer conformational.
So The Gauche Conformation, While It's Staggered, This Is More Stable Than Our Eclipsed Conformations.
Due to this rotation of the.
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1) fully eclipsed, when the methyl groups eclipse each other;
Depict The Staggered And Eclipsed Conformers Of Propane (Or A Similar Compound) Using Sawhorse Representations.
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Representation of eclipsed and staggered conformation:
Staggered Conformation Is A Low Strain.
1) as dgs has noted, the gauche conformation of ethylene glycol is stabilized by the formation of an intramolecular hydrogen bond and remains the preferred.
The Staggered Conformation Has A Lower Potential Energy And The Eclipsed Conformation Has A Higher Potential Energy.