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?

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

Draw the cis and trans structures of hex-2-ene. Which isomer will have higher boiling point and why?

The number of stereoisomers obtained by bromination of trans- 2 - butene is

In the dehydrohalogenatino of 2-bromobutane, which conformation leads to the formation of cis-2 butene

Give plausible explanation for each of the following : i) Why are AMINES less acidic than alcohols of comparable molecular masses? iii) Why do primary AMINES have higher boiling point than tertiary AMINES? iii) Why are aliphatic AMINES stronger bases than aromatic AMINES?

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.