The basic ring structure of the given compound representing the different hydrogen atoms in it is to be drawn. Further, the hydrogen atoms are to be categorized as equatorial or axial. Concept Introduction: > Chair conformations: It is the most stable conformation, which accurately shows the spatial arrangement of atoms. > Equatorial bonds are parallel to the average plane of the ring, while axial bonds are perpendicular to the average plane of the ring. > The conformation having bonds at the equatorial positions are more stable than those with bonds at the axial position. > On flipping the cyclohexane ring, axial bonds become equatorial bonds and equatorial bonds becomes axial bond. > Bulkier group acquires equatorial positions to form stable conformer due to steric factors > The organic compounds which are biologically active and consist of four ring structures arranged in a specific order are referred to as steroids. They are the derivatives of compounds of the perhydrocyclopentanophenanthrene ring system. > The carbon atom forms bond with the hydrogen atom, in order to complete its valency of 4, and the hydrogen atoms are regarded as axial or equatorial based on the plane in which they are present.

Question

Want to see the full answer?

Answer 1

Question

Chapter 23, Problem 6PP

Interpretation Introduction

Interpretation:

The basic ring structure of the given compound representing the different hydrogen atoms in it is to be drawn. Further, the hydrogen atoms are to be categorized as equatorial or axial.

Concept Introduction:
>
Chair conformations: It is the most stable conformation, which accurately shows the spatial arrangement of atoms.
>
Equatorial bonds are parallel to the average plane of the ring, while axial bonds are perpendicular to the average plane of the ring.
>
The conformation having bonds at the equatorial positions are more stable than those with bonds at the axial position.
>
On flipping the cyclohexane ring, axial bonds become equatorial bonds and equatorial bonds becomes axial bond.
>
Bulkier group acquires equatorial positions to form stable conformer due to steric factors
>
The organic compounds which are biologically active and consist of four ring structures arranged in a specific order are referred to as steroids. They are the derivatives of compounds of the perhydrocyclopentanophenanthrene ring system.
>
The carbon atom forms bond with the hydrogen atom, in order to complete its valency of 4, and the hydrogen atoms are regarded as axial or equatorial based on the plane in which they are present.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Predict the major products of the following organic reaction: O O + A ? Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. Explanation Check Click and drag to start drawing a structure. eserved. Terms of Use | Privacy Center >

(EXM 2, PRBLM 3) Here is this problem, can you explain it to me and show how its done. Thank you I need to see the work for like prbl solving.

can someone draw out the reaction mechanism for this reaction showing all bonds, intermediates and side products Comment on the general features of the 1H-NMR spectrum of isoamyl ester provided below