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Organic And Biological Chemistry

7th Edition
STOKER + 1 other
ISBN: 9781305081079

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BuyFindarrow_forward

Organic And Biological Chemistry

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

Assign an IUPAC name to each of the following cycloalkanes.

a. Chapter 1, Problem 1.101EP, Assign an IUPAC name to each of the following cycloalkanes. a. b. c. d. , example  1

b. Chapter 1, Problem 1.101EP, Assign an IUPAC name to each of the following cycloalkanes. a. b. c. d. , example  2

c. Chapter 1, Problem 1.101EP, Assign an IUPAC name to each of the following cycloalkanes. a. b. c. d. , example  3

d. Chapter 1, Problem 1.101EP, Assign an IUPAC name to each of the following cycloalkanes. a. b. c. d. , example  4

(a)

Interpretation Introduction

Interpretation:

The IUPAC name for the given cycloalkane has to be written.

Concept Introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).  IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule.  It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.

Root word represents the longest continuous carbon skeleton of the organic molecule.

The IUPAC name for cycloalkane can be obtained simply by adding prefix cyclo- before the alkane name which corresponds to the total number of carbon atoms that are present in the ring.  To name a cycloalkane, the first step is to find the longest carbon chain that makes a cyclic ring without any unsaturation.  The next step is to identify the substituents that are present in the cyclic ring structure.  The numbering has to be given in a way that the substituents get the least numbering.

Explanation

Given structure is,

From the given structure the lengthy carbon chain that makes a cyclic structure has to be identified.  In this case it is a five carbon cyclic chain...

(b)

Interpretation Introduction

Interpretation:

The IUPAC name for the given cycloalkane has to be written.

Concept Introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).  IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule.  It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.

Root word represents the longest continuous carbon skeleton of the organic molecule.

The IUPAC name for cycloalkane can be obtained simply by adding prefix cyclo- before the alkane name which corresponds to the total number of carbon atoms that are present in the ring.  To name a cycloalkane, the first step is to find the longest carbon chain that makes a cyclic ring without any unsaturation.  The next step is to identify the substituents that are present in the cyclic ring structure.  The numbering has to be given in a way that the substituents get the least numbering.

(c)

Interpretation Introduction

Interpretation:

The IUPAC name for the given cycloalkane has to be written.

Concept Introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).  IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule.  It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.

Root word represents the longest continuous carbon skeleton of the organic molecule.

The IUPAC name for cycloalkane can be obtained simply by adding prefix cyclo- before the alkane name which corresponds to the total number of carbon atoms that are present in the ring.  To name a cycloalkane, the first step is to find the longest carbon chain that makes a cyclic ring without any unsaturation.  The next step is to identify the substituents that are present in the cyclic ring structure.  The numbering has to be given in a way that the substituents get the least numbering.

(d)

Interpretation Introduction

Interpretation:

The IUPAC name for the given cycloalkane has to be written.

Concept Introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).  IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule.  It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.

Root word represents the longest continuous carbon skeleton of the organic molecule.

The IUPAC name for cycloalkane can be obtained simply by adding prefix cyclo- before the alkane name which corresponds to the total number of carbon atoms that are present in the ring.  To name a cycloalkane, the first step is to find the longest carbon chain that makes a cyclic ring without any unsaturation.  The next step is to identify the substituents that are present in the cyclic ring structure.  The numbering has to be given in a way that the substituents get the least numbering.

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Sect-1.5 P-2QQSect-1.5 P-3QQSect-1.6 P-1QQSect-1.6 P-2QQSect-1.6 P-3QQSect-1.6 P-4QQSect-1.7 P-1QQSect-1.7 P-2QQSect-1.8 P-1QQSect-1.8 P-2QQSect-1.8 P-3QQSect-1.8 P-4QQSect-1.8 P-5QQSect-1.8 P-6QQSect-1.8 P-7QQSect-1.9 P-1QQSect-1.9 P-2QQSect-1.10 P-1QQSect-1.10 P-2QQSect-1.11 P-1QQSect-1.11 P-2QQSect-1.11 P-3QQSect-1.12 P-1QQSect-1.12 P-2QQSect-1.12 P-3QQSect-1.13 P-1QQSect-1.13 P-2QQSect-1.13 P-3QQSect-1.14 P-1QQSect-1.14 P-2QQSect-1.14 P-3QQSect-1.15 P-1QQSect-1.15 P-2QQSect-1.16 P-1QQSect-1.16 P-2QQSect-1.16 P-3QQSect-1.17 P-1QQSect-1.17 P-2QQSect-1.17 P-3QQSect-1.17 P-4QQSect-1.18 P-1QQSect-1.18 P-2QQSect-1.18 P-3QQSect-1.18 P-4QQCh-1 P-1.1EPCh-1 P-1.2EPCh-1 P-1.3EPCh-1 P-1.4EPCh-1 P-1.5EPCh-1 P-1.6EPCh-1 P-1.7EPCh-1 P-1.8EPCh-1 P-1.9EPCh-1 P-1.10EPCh-1 P-1.11EPCh-1 P-1.12EPCh-1 P-1.13EPCh-1 P-1.14EPCh-1 P-1.15EPCh-1 P-1.16EPCh-1 P-1.17EPCh-1 P-1.18EPCh-1 P-1.19EPCh-1 P-1.20EPCh-1 P-1.21EPCh-1 P-1.22EPCh-1 P-1.23EPCh-1 P-1.24EPCh-1 P-1.25EPCh-1 P-1.26EPCh-1 P-1.27EPCh-1 P-1.28EPCh-1 P-1.29EPCh-1 P-1.30EPCh-1 P-1.31EPCh-1 P-1.32EPCh-1 P-1.33EPCh-1 P-1.34EPCh-1 P-1.35EPCh-1 P-1.36EPCh-1 P-1.37EPCh-1 P-1.38EPCh-1 P-1.39EPCh-1 P-1.40EPCh-1 P-1.41EPCh-1 P-1.42EPCh-1 P-1.43EPCh-1 P-1.44EPCh-1 P-1.45EPCh-1 P-1.46EPCh-1 P-1.47EPCh-1 P-1.48EPCh-1 P-1.49EPCh-1 P-1.50EPCh-1 P-1.51EPCh-1 P-1.52EPCh-1 P-1.53EPCh-1 P-1.54EPCh-1 P-1.55EPCh-1 P-1.56EPCh-1 P-1.57EPCh-1 P-1.58EPCh-1 P-1.59EPCh-1 P-1.60EPCh-1 P-1.61EPCh-1 P-1.62EPCh-1 P-1.63EPCh-1 P-1.64EPCh-1 P-1.65EPCh-1 P-1.66EPCh-1 P-1.67EPCh-1 P-1.68EPCh-1 P-1.69EPCh-1 P-1.70EPCh-1 P-1.71EPCh-1 P-1.72EPCh-1 P-1.73EPCh-1 P-1.74EPCh-1 P-1.75EPCh-1 P-1.76EPCh-1 P-1.77EPCh-1 P-1.78EPCh-1 P-1.79EPCh-1 P-1.80EPCh-1 P-1.81EPCh-1 P-1.82EPCh-1 P-1.83EPCh-1 P-1.84EPCh-1 P-1.85EPCh-1 P-1.86EPCh-1 P-1.87EPCh-1 P-1.88EPCh-1 P-1.89EPCh-1 P-1.90EPCh-1 P-1.91EPCh-1 P-1.92EPCh-1 P-1.93EPCh-1 P-1.94EPCh-1 P-1.95EPCh-1 P-1.96EPCh-1 P-1.97EPCh-1 P-1.98EPCh-1 P-1.99EPCh-1 P-1.100EPCh-1 P-1.101EPCh-1 P-1.102EPCh-1 P-1.103EPCh-1 P-1.104EPCh-1 P-1.105EPCh-1 P-1.106EPCh-1 P-1.107EPCh-1 P-1.108EPCh-1 P-1.109EPCh-1 P-1.110EPCh-1 P-1.111EPCh-1 P-1.112EPCh-1 P-1.113EPCh-1 P-1.114EPCh-1 P-1.115EPCh-1 P-1.116EPCh-1 P-1.117EPCh-1 P-1.118EPCh-1 P-1.119EPCh-1 P-1.120EPCh-1 P-1.121EPCh-1 P-1.122EPCh-1 P-1.123EPCh-1 P-1.124EPCh-1 P-1.125EPCh-1 P-1.126EPCh-1 P-1.127EPCh-1 P-1.128EPCh-1 P-1.129EPCh-1 P-1.130EPCh-1 P-1.131EPCh-1 P-1.132EPCh-1 P-1.133EPCh-1 P-1.134EPCh-1 P-1.135EPCh-1 P-1.136EPCh-1 P-1.137EPCh-1 P-1.138EPCh-1 P-1.139EPCh-1 P-1.140EPCh-1 P-1.141EPCh-1 P-1.142EPCh-1 P-1.143EPCh-1 P-1.144EPCh-1 P-1.145EPCh-1 P-1.146EPCh-1 P-1.147EPCh-1 P-1.148EP

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