Skip to main content

Science Chemistry Organic Chemistry

(a) Interpretation: The conversion of ball-and-stick model to a skeletal structure that clearly shows the stereochemistry at the ring fusion of given decalin derivative is to be stated. Concept introduction: Decalin and its derivatives involve fusion of two six-membered rings that share a C − C bond. The substituents present at ring fusion are identified as cis or trans. If substituents present at ring fusion are present opposite sides to each other, then it is identified as trans, and if substituents present at ring fusion are present same sides to each other, then it is identified as cis.

(a) Interpretation: The conversion of ball-and-stick model to a skeletal structure that clearly shows the stereochemistry at the ring fusion of given decalin derivative is to be stated. Concept introduction: Decalin and its derivatives involve fusion of two six-membered rings that share a C − C bond. The substituents present at ring fusion are identified as cis or trans. If substituents present at ring fusion are present opposite sides to each other, then it is identified as trans, and if substituents present at ring fusion are present same sides to each other, then it is identified as cis.

Solution Summary: The author explains that the skeletal structure of the given decalin is shown in Figure 1.

Organic Chemistry

Organic Chemistry

5th Edition

ISBN: 9780078021558

Author: Janice Gorzynski Smith Dr.

Publisher: McGraw-Hill Education

See similar textbooks

Concept explainers

Carbohydrates are the organic compounds that are obtained in foods and living matters in the shape of sugars, cellulose, and starch. The general formula of carbohydrates is Cn(H2O)2. The ratio of H and O present in carbohydrates is identical to water.

Starch is a polysaccharide carbohydrate that belongs to the category of polysaccharide carbohydrates.

The rotation of a particular structure of the chiral compound because of the epimerization is called mutarotation. It is the repercussion of the ring chain tautomerism. In terms of glucose, this can be defined as the modification in the equilibrium of th…

A chemical compound that is represented with a molecular formula C6H12O6 is called L-(-) sugar. At the carbon’s 5th position, the hydroxyl group is placed to the compound’s left and therefore the sugar is represented as L(-)-sugar. It is capable of rotat…

Question

Chapter 31, Problem 31.18P

Interpretation Introduction

(a)

Interpretation: The conversion of ball-and-stick model to a skeletal structure that clearly shows the stereochemistry at the ring fusion of given decalin derivative is to be stated.

Concept introduction: Decalin and its derivatives involve fusion of two six-membered rings that share a C−C bond. The substituents present at ring fusion are identified as cis or trans. If substituents present at ring fusion are present opposite sides to each other, then it is identified as trans, and if substituents present at ring fusion are present same sides to each other, then it is identified as cis.

Interpretation Introduction

(b)

Interpretation: The conversion of ball-and-stick model to a skeletal structure that clearly shows the stereochemistry at the ring fusion of given decalin derivative is to be stated.

Concept introduction: Decalin and its derivatives involve fusion of two six-membered rings that share a C−C bond. The substituents present at ring fusion are identified as cis or trans. If substituents present at ring fusion are present opposite sides to each other, then it is identified as trans, and if substituents present at ring fusion are present same sides to each other, then it is identified as cis.

Expert Solution & Answer

bartleby

Trending nowThis is a popular solution!

Check out sample textbook solution

Blurred answer

Chapter 31, Problem 31.17P

Chapter 31, Problem 31.19P

Students have asked these similar questions

Provide the correct common name for the compound shown here.

Ph heat heat

(12) Which one of the following statements about fluo- rometry is FALSE? a) Fluorescence is better detected at 90 from the exci- tation direction. b) Fluorescence is typically shifted to longer wave- length from the excitation wavelength. c) For most fluorescent compounds, radiation is pro- duced by a transition

Chapter 31 Solutions

Organic Chemistry

Ch. 31 - Problem 31.1 One component of jojoba oil is a wax...Ch. 31 - Problem 31.2 How would you expect the melting...Ch. 31 - Problem 31.3 Draw the products formed when...Ch. 31 - Problem 31.4 The main fatty acid component of the...Ch. 31 - Prob. 31.5P Ch. 31 - Problem 31.6 Draw the structure of a lecithin...Ch. 31 - Prob. 31.7P Ch. 31 - Problem 31.8 Why are phospholipids, but not...Ch. 31 - Problem 31.9 Explain why regularly ingesting a...Ch. 31 - Problem 31.10 Locate the isoprene units in each...

Ch. 31 - Problem 31.11 Locate the isoprene units in...Ch. 31 - Problem 31.12 Write a stepwise mechanism for the...Ch. 31 - Prob. 31.13P Ch. 31 - Prob. 31.14P Ch. 31 - Prob. 31.15P Ch. 31 - Prob. 31.16P Ch. 31 - 31.17 Locate the isoprene units in each...Ch. 31 - Prob. 31.18P Ch. 31 - Prob. 31.19P Ch. 31 - Prob. 31.20P Ch. 31 - Prob. 31.21P Ch. 31 - 31.22 What is the structure of an optically...Ch. 31 - Prob. 31.23P Ch. 31 - 31.24 Draw the structure of the following...Ch. 31 - Prob. 31.25P Ch. 31 - Locate the isoprene units in each compound. a. e....Ch. 31 - 31.27 Classify each terpene and terpenoid in...Ch. 31 - 31.38 Draw the products formed when cholesterol is...Ch. 31 - 31.29 An isoprene unit can be thought of as having...Ch. 31 - 31.30 Draw a stepwise mechanism for the conversion...Ch. 31 - Prob. 31.31P Ch. 31 - Prob. 31.32P Ch. 31 - Draw three-dimensional structures f or each...Ch. 31 - Prob. 31.34P Ch. 31 - Prob. 31.35P Ch. 31 - Prob. 31.36P Ch. 31 - Prob. 31.37P Ch. 31 - 31.38 Draw the products formed when cholesterol is...Ch. 31 - 31.39 Draw a stepwise mechanism for the following...Ch. 31 - 31.40 Draw a stepwise mechanism for the following...Ch. 31 - Prob. 31.41P

Knowledge Booster

Background pattern image

Chemistry

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

SEE MORE QUESTIONS

Recommended textbooks for you

Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning

Text book image

Organic Chemistry

Chemistry

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:Cengage Learning

SEE MORE TEXTBOOKS