Organic Chemistry Plus Masteringchemistry With Pearson Etext, Global Edition
Organic Chemistry Plus Masteringchemistry With Pearson Etext, Global Edition
9th Edition
ISBN: 9781292151229
Author: Wade, LeRoy G.
Publisher: PEARSON
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Chapter 3.3B, Problem 3.6P

(a)

Interpretation Introduction

To determine: The structures and names corresponding to the five isomers of C6H14.

Interpretation: The structures and names corresponding to the five isomers of C6H14 is to be stated.

Concept introduction: The rules for the naming of alkanes are stated below.

  • Firstly the longest carbon chain is chosen and the naming of chain is done according to the number of carbon atoms that are present in the chain.
  • Numbering of the chain is done in such a way that the substituent groups are placed at the lowest position.
  • Naming of substituent groups is done by the replacing of –ane with –yl.
  • If different types of substituent groups are present then they are written in an alphabetical order.
  • If a substituent is present more than one time then prefixes like di, tri, tetra are used depending on the number of times that particular substituent group appears in the chain.

(b)

Interpretation Introduction

To determine: The structures and names corresponding to the nine isomers of C7H16.

Interpretation: The structures and names corresponding to the nine isomers of C7H16 is to be stated.

Concept introduction: The rules for the naming of alkanes are stated below.

  • Firstly the longest carbon chain is chosen and the naming of chain is done according to the number of carbon atoms that are present in the chain.
  • Numbering of the chain is done in such a way that the substituent groups are placed at the lowest position.
  • Naming of substituent groups is done by the replacing of –ane with –yl.
  • If different types of substituent groups are present then they are written in an alphabetical order.
  • If a substituent is present more than one time then prefixes like di, tri, tetra are used depending on the number of times that particular substituent group appears in the chain.

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Chapter 3 Solutions

Organic Chemistry Plus Masteringchemistry With Pearson Etext, Global Edition

Ch. 3.7B - Prob. 3.11PCh. 3.7C - Draw a graph similar to Figure 3-9, of the...Ch. 3.8B - Draw a graph similar to Figure 3-11, of the...Ch. 3.9 - Draw a perspective representation of the most...Ch. 3.10C - Give IUPAC names for the following compounds.Ch. 3.10C - Draw the structure and give the molecular formula...Ch. 3.11 - Which of the following cycloalkanes are capable of...Ch. 3.11 - Give IUPAC names for the following cycloalkanes.Ch. 3.12B - The heat of combustion of...Ch. 3.12C - Prob. 3.20PCh. 3.13B - The cyclohexane chair shown in Figure 3-22 has the...Ch. 3.13B - Draw 1,2,3,4,5,6-hexamethylcyclohexane with all...Ch. 3.14 - Prob. 3.23PCh. 3.14 - Prob. 3.24PCh. 3.14 - Draw the most stable conformation of a....Ch. 3.15 - Prob. 3.26PCh. 3.15 - a. Draw both chair conformations of cis-1...Ch. 3.15 - Prob. 3.28PCh. 3.15A - Draw the two chair conformations of each of the...Ch. 3.15B - Draw the most stable conformation of a....Ch. 3.16A - Name the following compounds.Ch. 3.16B - Prob. 3.32PCh. 3 - Prob. 3.33SPCh. 3 - Prob. 3.34SPCh. 3 - 3-35 a. Draw and name the five cycloalkane...Ch. 3 - Draw the structure that corresponds with each...Ch. 3 - Each of the following descriptions applies to more...Ch. 3 - Write structures for a homologous series of...Ch. 3 - Prob. 3.39SPCh. 3 - Construct a graph, similar to Figure 3-11, of the...Ch. 3 - The following names are all incorrect or...Ch. 3 - In each pair of compounds, which compound has the...Ch. 3 - There are eight different five-carbon alkyl...Ch. 3 - Use a Newman projection about the indicated bond...Ch. 3 - a. Draw the two chair conformations of...Ch. 3 - Draw the two chair conformations of each compound,...Ch. 3 - Using what you know about the conformational...Ch. 3 - Prob. 3.48SPCh. 3 - Draw Newman projections along the C3C4 bond to...Ch. 3 - Prob. 3.50SPCh. 3 - The most stable form of the common sugar glucose...Ch. 3 - This is a Newman projection of a substituted...
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