BuyFindarrow_forward

Organic And Biological Chemistry

7th Edition
STOKER + 1 other
ISBN: 9781305081079

Solutions

Chapter
Section
BuyFindarrow_forward

Organic And Biological Chemistry

7th Edition
STOKER + 1 other
ISBN: 9781305081079
Textbook Problem

Assign an IUPAC name to each of the following unsaturated hydrocarbons.

  1. a. CH3—CH2— CH2—CH2—C=CH

Chapter 2, Problem 2.89EP, Assign an IUPAC name to each of the following unsaturated hydrocarbons. a. CH3CH2 CH2CH2C=CH , example  1

Chapter 2, Problem 2.89EP, Assign an IUPAC name to each of the following unsaturated hydrocarbons. a. CH3CH2 CH2CH2C=CH , example  2

Chapter 2, Problem 2.89EP, Assign an IUPAC name to each of the following unsaturated hydrocarbons. a. CH3CH2 CH2CH2C=CH , example  3

(a)

Interpretation Introduction

Interpretation:

The IUPAC name for the given unsaturated hydrocarbon has to be assigned.

Concept Introduction:

IUPAC nomenclature for alkyne:

  • The suffix –ane has to be replaced with the suffix –yne. This is used to indicate the presence of triple bond.
  • The longest continuous chain of carbon atoms has to be chosen that contains both carbon atoms of the triple bond.
  • The parent carbon chain has to be numbered in a way so that the numbering begins at the end near to the triple bond. In case if the triple bond is equidistant from both ends, then numbering has to be done from the end that is closer to substituents.
  • The position of the triple bond has to be given a single number which is lower‑numbered carbon atom that is present in the triple bond.
  • Suffixes like –diyne, -triyne, -tetryne, and so on are used when the compound contains more than one triple bond.
Explanation

Given structure of unsaturated hydrocarbon is,

The parent carbon chain is found to contain six carbon atoms. Therefore, the parent carbon is hexane.

As a triple bond is present in the parent carbon chain, the suffix –ane is replaced by –yne...

(b)

Interpretation Introduction

Interpretation:

The IUPAC name for the given unsaturated hydrocarbon has to be assigned.

Concept Introduction:

IUPAC nomenclature for alkyne:

  • The suffix –ane has to be replaced with the suffix –yne. This is used to indicate the presence of triple bond.
  • The longest continuous chain of carbon atoms has to be chosen that contains both carbon atoms of the triple bond.
  • The parent carbon chain has to be numbered in a way so that the numbering begins at the end near to the triple bond. In case if the triple bond is equidistant from both ends, then numbering has to be done from the end that is closer to substituents.
  • The position of the triple bond has to be given a single number which is lower‑numbered carbon atom that is present in the triple bond.
  • Suffixes like –diyne, -triyne, -tetryne, and so on are used when the compound contains more than one triple bond.

(c)

Interpretation Introduction

Interpretation:

The IUPAC name for the given unsaturated hydrocarbon has to be assigned.

Concept Introduction:

IUPAC nomenclature for alkyne:

  • The suffix –ane has to be replaced with the suffix –yne. This is used to indicate the presence of triple bond.
  • The longest continuous chain of carbon atoms has to be chosen that contains both carbon atoms of the triple bond.
  • The parent carbon chain has to be numbered in a way so that the numbering begins at the end near to the triple bond. In case if the triple bond is equidistant from both ends, then numbering has to be done from the end that is closer to substituents.
  • The position of the triple bond has to be given a single number which is lower‑numbered carbon atom that is present in the triple bond.
  • Suffixes like –diyne, -triyne, -tetryne, and so on are used when the compound contains more than one triple bond.

(d)

Interpretation Introduction

Interpretation:

The IUPAC name for the given unsaturated hydrocarbon has to be assigned.

Concept Introduction:

IUPAC nomenclature for alkyne:

  • The suffix –ane has to be replaced with the suffix –yne. This is used to indicate the presence of triple bond.
  • The longest continuous chain of carbon atoms has to be chosen that contains both carbon atoms of the triple bond.
  • The parent carbon chain has to be numbered in a way so that the numbering begins at the end near to the triple bond. In case if the triple bond is equidistant from both ends, then numbering has to be done from the end that is closer to substituents.
  • The position of the triple bond has to be given a single number which is lower‑numbered carbon atom that is present in the triple bond.
  • Suffixes like –diyne, -triyne, -tetryne, and so on are used when the compound contains more than one triple bond.

Still sussing out bartleby?

Check out a sample textbook solution.

See a sample solution

The Solution to Your Study Problems

Bartleby provides explanations to thousands of textbook problems written by our experts, many with advanced degrees!

Get Started
Sect-2.3 P-4QQSect-2.4 P-1QQSect-2.4 P-2QQSect-2.5 P-1QQSect-2.5 P-2QQSect-2.5 P-3QQSect-2.6 P-1QQSect-2.6 P-2QQSect-2.6 P-3QQSect-2.7 P-1QQSect-2.7 P-2QQSect-2.7 P-3QQSect-2.8 P-1QQSect-2.8 P-2QQSect-2.9 P-1QQSect-2.9 P-2QQSect-2.10 P-1QQSect-2.10 P-2QQSect-2.10 P-3QQSect-2.10 P-4QQSect-2.10 P-5QQSect-2.11 P-1QQSect-2.11 P-2QQSect-2.11 P-3QQSect-2.11 P-4QQSect-2.11 P-5QQSect-2.12 P-1QQSect-2.12 P-2QQSect-2.12 P-3QQSect-2.12 P-4QQSect-2.12 P-5QQSect-2.13 P-1QQSect-2.13 P-2QQSect-2.13 P-3QQSect-2.14 P-1QQSect-2.14 P-2QQSect-2.14 P-3QQSect-2.14 P-4QQSect-2.15 P-1QQSect-2.15 P-2QQSect-2.15 P-3QQSect-2.15 P-4QQSect-2.16 P-1QQSect-2.16 P-2QQCh-2 P-2.1EPCh-2 P-2.2EPCh-2 P-2.3EPCh-2 P-2.4EPCh-2 P-2.5EPCh-2 P-2.6EPCh-2 P-2.7EPCh-2 P-2.8EPCh-2 P-2.9EPCh-2 P-2.10EPCh-2 P-2.11EPCh-2 P-2.12EPCh-2 P-2.13EPCh-2 P-2.14EPCh-2 P-2.15EPCh-2 P-2.16EPCh-2 P-2.17EPCh-2 P-2.18EPCh-2 P-2.19EPCh-2 P-2.20EPCh-2 P-2.21EPCh-2 P-2.22EPCh-2 P-2.23EPCh-2 P-2.24EPCh-2 P-2.25EPCh-2 P-2.26EPCh-2 P-2.27EPCh-2 P-2.28EPCh-2 P-2.29EPCh-2 P-2.30EPCh-2 P-2.31EPCh-2 P-2.32EPCh-2 P-2.33EPCh-2 P-2.34EPCh-2 P-2.35EPCh-2 P-2.36EPCh-2 P-2.37EPCh-2 P-2.38EPCh-2 P-2.39EPCh-2 P-2.40EPCh-2 P-2.41EPCh-2 P-2.42EPCh-2 P-2.43EPCh-2 P-2.44EPCh-2 P-2.45EPCh-2 P-2.46EPCh-2 P-2.47EPCh-2 P-2.48EPCh-2 P-2.49EPCh-2 P-2.50EPCh-2 P-2.51EPCh-2 P-2.52EPCh-2 P-2.53EPCh-2 P-2.54EPCh-2 P-2.55EPCh-2 P-2.56EPCh-2 P-2.57EPCh-2 P-2.58EPCh-2 P-2.59EPCh-2 P-2.60EPCh-2 P-2.61EPCh-2 P-2.62EPCh-2 P-2.63EPCh-2 P-2.64EPCh-2 P-2.65EPCh-2 P-2.66EPCh-2 P-2.67EPCh-2 P-2.68EPCh-2 P-2.69EPCh-2 P-2.70EPCh-2 P-2.71EPCh-2 P-2.72EPCh-2 P-2.73EPCh-2 P-2.74EPCh-2 P-2.75EPCh-2 P-2.76EPCh-2 P-2.77EPCh-2 P-2.78EPCh-2 P-2.79EPCh-2 P-2.80EPCh-2 P-2.81EPCh-2 P-2.82EPCh-2 P-2.83EPCh-2 P-2.84EPCh-2 P-2.85EPCh-2 P-2.86EPCh-2 P-2.87EPCh-2 P-2.88EPCh-2 P-2.89EPCh-2 P-2.90EPCh-2 P-2.91EPCh-2 P-2.92EPCh-2 P-2.93EPCh-2 P-2.94EPCh-2 P-2.95EPCh-2 P-2.96EPCh-2 P-2.97EPCh-2 P-2.98EPCh-2 P-2.99EPCh-2 P-2.100EPCh-2 P-2.101EPCh-2 P-2.102EPCh-2 P-2.103EPCh-2 P-2.104EPCh-2 P-2.105EPCh-2 P-2.106EPCh-2 P-2.107EPCh-2 P-2.108EPCh-2 P-2.109EPCh-2 P-2.110EPCh-2 P-2.111EPCh-2 P-2.112EPCh-2 P-2.113EPCh-2 P-2.114EPCh-2 P-2.115EPCh-2 P-2.116EPCh-2 P-2.117EPCh-2 P-2.118EPCh-2 P-2.119EPCh-2 P-2.120EPCh-2 P-2.121EPCh-2 P-2.122EPCh-2 P-2.123EPCh-2 P-2.124EPCh-2 P-2.125EPCh-2 P-2.126EPCh-2 P-2.127EPCh-2 P-2.128EPCh-2 P-2.129EPCh-2 P-2.130EP

Additional Science Solutions

Find more solutions based on key concepts

Show solutions add

Distinguish between the terms aerobic and anaerobic.

Chemistry for Today: General, Organic, and Biochemistry

When consumers guess at the calorie values in restaurant food portions, they generally overestimate. T F

Nutrition: Concepts and Controversies - Standalone book (MindTap Course List)

Which of the following equations are dimensionally correct? (a) vf = vi + ax (b) y = (2 m) cos (kx), where k = ...

Physics for Scientists and Engineers, Technology Update (No access codes included)

Where is oceanic primary productivity highest?

Oceanography: An Invitation To Marine Science, Loose-leaf Versin