Boat conformation of cyclohexane has lower angle strain. But it has torsional strain associated with eclipsed bonds at the four of the carbon atoms that form the side of the boat. In addition steric interaction of the hydrogen atoms known as flagpole interaction destabilises the boat conformation and it's energy higher than the twisted boat conformation.
The twisted boat conformation relieves some of the torsional strain of the boat and moves the flagpole hydrogen further apart reducing the steric strain. So it's energy is lower than the boat conformation and consequently it is slightly more stable than the boat conformation.
6) The twisted boat conformation of cyclohexane is actually a slightly lower energy conformation than the...
6. Build the cyclobutane ring and study the angle strain and torsional strain. Draw the structures to explain these factors. 7. The conformation of cyclobutane is slightly folded. Folding gives partial relief from the eclipsing of bonds, as shown in the Newman projection. Compare this actual structure with the hypothetical planar structure. Draw the relevant structures. 8. trans-1,2-Dimethylcyclobutane is more stable than cis-1,2-dimethylcyclobutane, but cis-1,3- dimethylcyclobutane is more stable than trans-1,3-dimethylcyclobutane. Use the molecular models to find the reasons for...