EBK STUDY GUIDE/SOLUTIONS MANUAL FOR OR
EBK STUDY GUIDE/SOLUTIONS MANUAL FOR OR
8th Edition
ISBN: 9781319255572
Author: SCHORE
Publisher: VST
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
Chapter 2, Problem 45P

(a)

Interpretation Introduction

Interpretation: The structures corresponding to 2-methyl-3-propylpentane should be drawn and the incorrect IUPAC names should be corrected.

Concept introduction: As per IUPAC recommendations longest chain found in a continuous manner in a branched molecule is chosen as parent chain.

The IUPAC name begins with prefix to designate the number of C atoms in the longest chosen parent alkane followed by the suffix −ane. The positions of side chains or substituents are indicated by lowest numeral places before prefix.

Names of branches that occur commonly as side chains are listed below:

  EBK STUDY GUIDE/SOLUTIONS MANUAL FOR OR, Chapter 2, Problem 45P , additional homework tip  1

(b)

Interpretation Introduction

Interpretation: The structures corresponding to 5-(1,1-dimethylpropyl)nonane should be drawn and the incorrect IUPAC names should be corrected.

Concept introduction: As per IUPAC recommendations longest chain found in a continuous manner in a branched molecule is chosen as parent chain.

The IUPAC name begins with prefix to designate the number of C atoms in the longest chosen parent alkane followed by the suffix −ane. The positions of side chains or substituents are indicated by lowest numeral places before prefix.

Names of branches that occur commonly as side chains are listed below:

  EBK STUDY GUIDE/SOLUTIONS MANUAL FOR OR, Chapter 2, Problem 45P , additional homework tip  2

(c)

Interpretation Introduction

Interpretation: The structures corresponding to 2,3,4-trimethyl-4-butylheptane should be drawn and the incorrect IUPAC names should be corrected.

Concept introduction: As per IUPAC recommendations longest chain found in a continuous manner in a branched molecule is chosen as parent chain.

The IUPAC name begins with prefix to designate the number of C atoms in the longest chosen parent alkane followed by the suffix −ane. The positions of side chains or substituents are indicated by lowest numeral places before prefix.

Names of branches that occur commonly as side chains are listed below:

  EBK STUDY GUIDE/SOLUTIONS MANUAL FOR OR, Chapter 2, Problem 45P , additional homework tip  3

(d)

Interpretation Introduction

Interpretation:The structures corresponding to 4-tert-butyl-5- isopropyhexane should be drawn and the incorrect IUPAC names should be corrected.

Concept introduction: As per IUPAC recommendations longest chain found in a continuous manner in a branched molecule is chosen as parent chain.

The IUPAC name begins with prefix to designate the number of C atoms in the longest chosen parent alkane followed by the suffix −ane. The positions of side chains or substituents are indicated by lowest numeral places before prefix.

Names of branches that occur commonly as side chains are listed below:

  EBK STUDY GUIDE/SOLUTIONS MANUAL FOR OR, Chapter 2, Problem 45P , additional homework tip  4

(e)

Interpretation Introduction

Interpretation: The structures corresponding to 4-(2-ethylbutyl)decane should be drawn and the incorrect IUPAC names should be corrected.

Concept introduction: As per IUPAC recommendations longest chain found in a continuous manner in a branched molecule is chosen as parent chain.

The IUPAC name begins with prefix to designate the number of C atoms in the longest chosen parent alkane followed by the suffix −ane. The positions of side chains or substituents are indicated by lowest numeral places before prefix.

Names of branches that occur commonly as side chains are listed below:

  EBK STUDY GUIDE/SOLUTIONS MANUAL FOR OR, Chapter 2, Problem 45P , additional homework tip  5

(f)

Interpretation Introduction

Interpretation:The structures corresponding to 2,4,4-trimethylpentane should be drawn and the incorrect IUPAC names should be corrected.

Concept introduction: As per IUPAC recommendations longest chain found in a continuous manner in a branched molecule is chosen as parent chain.

The IUPAC name begins with prefix to designate the number of C atoms in the longest chosen parent alkane followed by the suffix −ane. The positions of side chains or substituents are indicated by lowest numeral places before prefix.

Names of branches that occur commonly as side chains are listed below:

  EBK STUDY GUIDE/SOLUTIONS MANUAL FOR OR, Chapter 2, Problem 45P , additional homework tip  6

(g)

Interpretation Introduction

Interpretation: The structures corresponding to 4-sec-butylheptane should be drawn and the incorrect IUPAC names should be corrected.

Concept introduction: As per IUPAC recommendations longest chain found in a continuous manner in a branched molecule is chosen as parent chain.

The IUPAC name begins with prefix to designate the number of C atoms in the longest chosen parent alkane followed by the suffix −ane. The positions of side chains or substituents are indicated by lowest numeral places before prefix.

Names of branches that occur commonly as side chains are listed below:

  EBK STUDY GUIDE/SOLUTIONS MANUAL FOR OR, Chapter 2, Problem 45P , additional homework tip  7

(h)

Interpretation Introduction

Interpretation: The structures corresponding to isoheptane should be drawn and the incorrect IUPAC names should be corrected.

Concept introduction: As per IUPAC recommendations longest chain found in a continuous manner in a branched molecule is chosen as parent chain.

The IUPAC name begins with prefix to designate the number of C atoms in the longest chosen parent alkane followed by the suffix −ane. The positions of side chains or substituents are indicated by lowest numeral places before prefix.

Names of branches that occur commonly as side chains are listed below:

  EBK STUDY GUIDE/SOLUTIONS MANUAL FOR OR, Chapter 2, Problem 45P , additional homework tip  8

(i)

Interpretation Introduction

Interpretation: The structures corresponding to neoheptane should be drawn and the incorrect IUPAC names should be corrected.

Concept introduction: As per IUPAC recommendations longest chain found in a continuous manner in a branched molecule is chosen as parent chain.

The IUPAC name begins with prefix to designate the number of C atoms in the longest chosen parent alkane followed by the suffix −ane. The positions of side chains or substituents are indicated by lowest numeral places before prefix.

Names of branches that occur commonly as side chains are listed below:

  EBK STUDY GUIDE/SOLUTIONS MANUAL FOR OR, Chapter 2, Problem 45P , additional homework tip  9

Blurred answer
Students have asked these similar questions
I
Draw the anti-Markovnikov product of the hydration of this alkene. this problem. Note for advanced students: draw only one product, and don't worry about showing any stereochemistry. Drawing dash and wedge bonds has been disabled for esc esc ☐ Explanation Check F1 1 2 F2 # 3 F3 + $ 14 × 1. BH THE BH3 2. H O NaOH '2 2' Click and drag to start drawing a structure. F4 Q W E R A S D % 905 LL F5 F6 F7 © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility < & 6 7 27 8 T Y U G H I F8 F9 F10 F11 F12 9 0 J K L P + // command option Z X C V B N M H H rol option command
AG/F-2° V 3. Before proceeding with this problem you may want to glance at p. 466 of your textbook where various oxo-phosphorus derivatives and their oxidation states are summarized. Shown below are Latimer diagrams for phosphorus at pH values at 0 and 14: -0.93 +0.38 -0.50 -0.51 -0.06 H3PO4 →H4P206 →H3PO3 →→H3PO₂ → P → PH3 Acidic solution Basic solution -0.28 -0.50 3--1.12 -1.57 -2.05 -0.89 PO HPO H₂PO₂ →P → PH3 -1.73 a) Under acidic conditions, H3PO4 can be reduced into H3PO3 directly (-0.28V), or via the formation and reduction of H4P206 (-0.93/+0.38V). Calculate the values of AG's for both processes; comment. (3 points) 0.5 PH P 0.0 -0.5 -1.0- -1.5- -2.0 H.PO, -2.3+ -3 -2 -1 1 2 3 2 H,PO, b) Frost diagram for phosphorus under acidic conditions is shown. Identify possible disproportionation and comproportionation processes; write out chemical equations describing them. (2 points) H,PO 4 S Oxidation stale, N
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
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY
Chapter 4 Alkanes and Cycloalkanes Lesson 2; Author: Linda Hanson;https://www.youtube.com/watch?v=AL_CM_Btef4;License: Standard YouTube License, CC-BY
Chapter 4 Alkanes and Cycloalkanes Lesson 1; Author: Linda Hanson;https://www.youtube.com/watch?v=PPIa6EHJMJw;License: Standard Youtube License