Essential Organic Chemistry (3rd Edition)
Essential Organic Chemistry (3rd Edition)
3rd Edition
ISBN: 9780321937711
Author: Paula Yurkanis Bruice
Publisher: PEARSON
bartleby

Concept explainers

Question
Book Icon
Chapter 4.1, Problem 5P

(a)

Interpretation Introduction

Interpretation:

The skeletal structures for the given compounds has to be drawn including cis-trans isomers.

Concept introduction:

In skeletal structure or bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the heteroatoms are drawn as line segments.  For acyclic carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon.  For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.

Cis-trans terminology is used for two non-similar groups attached alkenes.

If the two identical groups are attached on each side of double bond in same side, then it is cis alkenes.

If the two identical groups are attached on each side of double bond in opposite manner, then it is Trans alkenes.

(b)

Interpretation Introduction

Interpretation:

The skeletal structures for the given compounds has to be drawn including cis-trans isomers.

Concept introduction:

In skeletal structure or bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the heteroatoms are drawn as line segments.  For acyclic carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon.  For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.

Cis-trans terminology is used for two non-similar groups attached alkenes.

If the two identical groups are attached on each side of double bond in same side, then it is cis alkenes.

If the two identical groups are attached on each side of double bond in opposite manner, then it is trans alkenes.

(c)

Interpretation Introduction

Interpretation:

The skeletal structures for the given compounds has to be drawn including cis-trans isomers.

Concept introduction:

In skeletal structure or bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the heteroatoms are drawn as line segments.  For acyclic carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon.  For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.

Cis-trans terminology is used for two non-similar groups attached alkenes.

If the two identical groups are attached on each side of double bond in same side, then it is cis alkenes.

If the two identical groups are attached on each side of double bond in opposite manner, then it is trans alkenes.

(d)

Interpretation Introduction

Interpretation:

The skeletal structures for the given compounds has to be drawn including cis-trans isomers.

Concept introduction:

In skeletal structure or bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the heteroatoms are drawn as line segments.  For acyclic carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon.  For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.

Cis-trans terminology is used for two non-similar groups attached alkenes.

If the two identical groups are attached on each side of double bond in same side, then it is cis alkenes.

If the two identical groups are attached on each side of double bond in opposite manner, then it is trans alkenes.

Blurred answer
Students have asked these similar questions
14.44 Ignoring stereoisomers, draw all products that form by addition of HBr to (E)-hexa-1,3,5-triene.
Include stereochemistry Leven though the solutions manual does 14.43 Draw the products formed when each compound is treated with one not) equivalent of HBr. a. b. C.
14.41 Label each pair of compounds as stereoisomers, conformations, or constitutional isomers: (a) A and B; (b) A and C; (c) A and D; (d) C and D. A B C D

Chapter 4 Solutions

Essential Organic Chemistry (3rd Edition)

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
Text book image
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
Text book image
Introductory Chemistry For Today
Chemistry
ISBN:9781285644561
Author:Seager
Publisher:Cengage
Text book image
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning