Organic Chemistry
Organic Chemistry
4th Edition
ISBN: 9780073402772
Author: Janice G. Smith
Publisher: MCG
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Chapter 30, Problem 30.37P
Interpretation Introduction

(a)

Interpretation: The three dimensional structure for the given steroid is to be drawn.

Concept introduction: In ball-and-stick model, each colored ball represents a specific atom and each stick represents a bond.

Interpretation Introduction

(b)

Interpretation: The structure of stereoisomer formed by the reduction of ketone group with H2, PdC is to be predicted and the reason why only one stereoisomer is formed is to be stated.

Concept introduction: Ring-flipping converts equatorial bonds into axial bonds and axial bonds into equatorial bonds. The reduction of ketone into alcohol can be done by using reagent H2 in the presence of palladium.

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a. Draw a three-dimensional structure for the following steroid. b. What is the structure of the single stereoisomer formed by reduction of this ketone wrth H2, Pd-C? Explain why only one stereoisomer is formed.
a. Draw a three-dimensional structure for the following steroid. b. What is the structure of the single stereoisomer formed by reduction of this ketone with H2, Pd-C? Explain why only one stereoisomer is formed.
1. What chemical structural differences are there between the monoterpenes and alkaloids? 2. What do you understand by ‘biogenic isoprene rule’? Who proposed these rule and what is the significance of these rule?

Chapter 30 Solutions

Organic Chemistry

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