Which of the following isomeric structures ha | vedclass

Name: Exam Paper Generator | JEE NEET Paper Generator | Vedclass
Brand: Vedclass
Rating: 5 (35 reviews)

Question

(D) The stability of cyclohexane derivatives in chair conformation depends on the equatorial $(e)$ vs axial $(a)$ orientation of substituents. Substit

Vedclass · Accepted Answer

Vedclass · Answer

(D) The stability of cyclohexane derivatives in chair conformation depends on the equatorial $(e)$ vs axial $(a)$ orientation of substituents. Substituents in the equatorial position are more stable due to reduced $1,3-$diaxial interactions. Analyzing the given structures: $A$: $1,2$-diaxial $(aa)$ $B$: $1,4$-diaxial $(aa)$ $C$: $1,3$-axial-equatorial $(ae)$ $D$: $1,3$-diequatorial $(ee)$ Structure $D$ has both methyl groups in the equatorial position,which minimizes steric repulsion and results in the lowest energy (highest stability).

Which of the following isomeric structures has the lowest energy?

Similar Questions

Among the following,the conformation that corresponds to the most stable conformation of meso-butane-$2,3$-diol is -

Define torsional strain.

How can you define skew conformation?

$HO-CH_2-CH_2-CHO$
Which conformer of the above compound is most stable (consider the conformer across the $C_2-C_3$ bond)?

Which statement is true for cyclohexane?

Vedclass Test Series

Exam Paper Generator

Online Exam Module