Which of the following statements is not true about conformational isomerism ?
Conformational isomers can be represented by newman and sawhorse projections. No. of conformational isomers of a compound is infinite. Generally, staggered form is most stable. Conformational isomerism is also found in cyclic compounds. Hence, Option "C" is the correct answer.
$$ \mu $$ 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 .
a) Draw Newman projection for the less stable staggered form of butane. b) Give reason for the relatively less stability of the staggered form.
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?