a) Draw Newman projection for the less stable staggered form of butane. b) Give reason for the relatively less stability of the staggered form.
a) Two Newman projections for the staggered form of butane of b) The less stability of such a form can be explained on the basis of van der waals strain because the groups are not at the maximum distance from each other.Thus,the repulsive forces between them are more than in form.
$$ \mu $$ observed = $$ \sum \mu_iX_i $$ where $$ \mu_i $$ is the dipole moment of the stable conformer and $$ X_i $$ is the mole fraction of that conformer. Write the stable conformer for $$ (Z - CH_2 - CH - Z) $$ in Newman's projection. If $$ \mu_{solution} = 1.0\,D $$ and mole fraction of the antiform $$ = 0.82 $$ , find the $$ \mu $$ gauche form .
Which of the following statements is not true about conformational isomerism ?
Give the Newman configuration of the least staggered form of n-butane. Due to which of the following strain it is destabilized?
What is the relationship between the molecules in the following pairs ?
For the following newman projection
Newman projections P, Q, R and S are shown below: Refer image, Which one of the following options represents identical molecules?