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 8PP

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

Please correct answer and don't used hand raiting don't used Ai solution

Please correct answer and don't used hand raiting

Answer 2

Question

Chapter 23, Problem 8PP

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

Answer 3

Question

Chapter 23, Problem 8PP

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

Answer 4

Question

Chapter 23, Problem 8PP

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

Answer 5

Chapter 23, Problem 8PP

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.

Answer 6

Chapter 23, Problem 8PP

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.

Answer 7

Chapter 23, Problem 8PP

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.

Answer 8

Expert Solution & Answer

Answer 9

Expert Solution & Answer

Answer 10

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 11

Ch. 23 - Prob. 1PP Ch. 23 - Prob. 2PP Ch. 23 - Prob. 3PP Ch. 23 - Prob. 4PP Ch. 23 - Prob. 5PP Ch. 23 - Prob. 6PP Ch. 23 - Prob. 7PP Ch. 23 - Prob. 8PP Ch. 23 - Prob. 9PP Ch. 23 - Prob. 10PP

Solution Summary: The author explains the basic ring structure of the given compound representing the different hydrogen atoms in it is to be drawn.

Concept explainers

Want to see the full answer?

Chapter 23 Solutions