Conformations are those special arrangements which are obtained by rotation around sigma bonds.
Draw the staggered and eclipsed conformation of ethane.

Conformations are those special arrangements which are obtained by rotation around sigma bonds. Why does cis-2-butene have a higher boiling point than trans-2-butene?

Draw the Newman projections for staggered and eclipsed conformations of ethane.

A spacial arrangements of atoms which can be converted into one another by rotation arround a C-C single bond are called conformations. i) Represent Sawhorse and Newman projection formulae of staggered and eclipsed conformation of ethane.

Draw the Newman projections of the eclipsed and staggered conformations of ethane molecule.

Draw the Newman's projections of the eclipsed and staggered conformations of n-butane.

A spacial arrangements of atoms which can be converted into one another by rotation arround a C-C single bond are called conformations. ii) Comapare the stabilities of staggered and eclipsed conformations.

Draw Sawhorse and Newman's projections of the different conformers of ethane.

Controlled oxidation of alkanes in the presence of suitable catalysts give a variety of products. Free rotation about a carbon - carbon single bond is permitted in an alkane molecule. What are conformers? Draw the structure of the eclipsed and staggered conformers of ethane in Sawhorse and Newman projection and explain their relative stability.

Draw the sawhorse projections for eclipsed and staggered forms of a ethane molecule.

Staggered conformation is more stable than eclipsed from because there is less repulsion between bond pairs of electrons. Draw the cls and trans structures of hex-2-ene.