Organic Chemistry Third Edition + Electronic Solutions Manual And Study Guide
Organic Chemistry Third Edition + Electronic Solutions Manual And Study Guide
3rd Edition
ISBN: 9781119351610
Author: David Klein
Publisher: Wiley Plus
Question
Book Icon
Chapter 4.2, Problem 12PTS

(a)

Interpretation Introduction

Interpretation: The bond-line structure of given compounds should be drawn.

Concept Introduction:

Nomenclature of organic chemicals:

The naming of the organic compound is given by IUPAC (International Union for pure and applied chemistry). In the IUPAC names consist of certain rules for giving chemical names they are,

  • The longer number of Carbon chain of a compound is identified this is called parent of the compound.
  • In the cyclic compounds the number of carbon involving in ring formation is called parent of the compound.
  • The compound have more than one parent chains means the larger number of substitutions present in the chain is consider as a parent chain.
  • The names of all substituents are arranged by alphabets to starts with lowest numbering.
  • The complex substituent is build by a substituent on a substituent so the branched substituent is called complex substituent.
  • In the complex substituent having compounds the substituent name is assigned by a name each of them based on numbers going away from the parent.

To draw the bond-line structure of given compounds.

(b)

Interpretation Introduction

Interpretation: The bond-line structure of given compounds should be drawn.

Concept Introduction:

Nomenclature of organic chemicals:

The naming of the organic compound is given by IUPAC (International Union for pure and applied chemistry). In the IUPAC names consist of certain rules for giving chemical names they are,

  • The longer number of Carbon chain of a compound is identified this is called parent of the compound.
  • In the cyclic compounds the number of carbon involving in ring formation is called parent of the compound.
  • The compound have more than one parent chains means the larger number of substitutions present in the chain is consider as a parent chain.
  • The names of all substituents are arranged by alphabets to starts with lowest numbering.
  • The complex substituent is build by a substituent on a substituent so the branched substituent is called complex substituent.
  • In the complex substituent having compounds the substituent name is assigned by a name each of them based on numbers going away from the parent.

To draw the bond-line structure of given compounds.

(c)

Interpretation Introduction

Interpretation: The bond-line structure of given compounds should be drawn.

Concept Introduction:

Nomenclature of organic chemicals:

The naming of the organic compound is given by IUPAC (International Union for pure and applied chemistry). In the IUPAC names consist of certain rules for giving chemical names they are,

  • The longer number of Carbon chain of a compound is identified this is called parent of the compound.
  • In the cyclic compounds the number of carbon involving in ring formation is called parent of the compound.
  • The compound have more than one parent chains means the larger number of substitutions present in the chain is consider as a parent chain.
  • The names of all substituents are arranged by alphabets to starts with lowest numbering.
  • The complex substituent is build by a substituent on a substituent so the branched substituent is called complex substituent.
  • In the complex substituent having compounds the substituent name is assigned by a name each of them based on numbers going away from the parent.

To draw the bond-line structure of given compounds.

Blurred answer
Students have asked these similar questions
A. B. b. Now consider the two bicyclic molecules A. and B. Note that A. is a dianion and B. is a neutral molecule. One of these molecules is a highly reactive compound first characterized in frozen noble gas matrices, that self-reacts rapidly at temperatures above liquid nitrogen temperature. The other compound was isolated at room temperature in the early 1960s, and is a stable ligand used in organometallic chemistry. Which molecule is the more stable molecule, and why?
Where are the chiral centers in this molecule? Also is this compound meso yes or no?
PLEASE HELP! URGENT!

Chapter 4 Solutions

Organic Chemistry Third Edition + Electronic Solutions Manual And Study Guide

Ch. 4.2 - Prob. 4LTSCh. 4.2 - Prob. 8PTSCh. 4.2 - Prob. 9PTSCh. 4.2 - Prob. 10ATSCh. 4.2 - Prob. 5LTSCh. 4.2 - Prob. 11PTSCh. 4.2 - Prob. 12PTSCh. 4.2 - Prob. 13ATSCh. 4.3 - Prob. 6LTSCh. 4.3 - Prob. 14PTSCh. 4.3 - Prob. 15ATSCh. 4.6 - Prob. 7LTSCh. 4.6 - Prob. 16PTSCh. 4.6 - Prob. 17ATSCh. 4.7 - Prob. 18CCCh. 4.8 - Prob. 8LTSCh. 4.8 - Prob. 19PTSCh. 4.8 - Prob. 20ATSCh. 4.11 - Prob. 9LTSCh. 4.11 - Prob. 21PTSCh. 4.11 - Prob. 22ATSCh. 4.11 - Prob. 10LTSCh. 4.11 - Prob. 23PTSCh. 4.11 - Prob. 24ATSCh. 4.12 - Prob. 11LTSCh. 4.12 - Prob. 25PTSCh. 4.12 - Prob. 26ATSCh. 4.12 - Prob. 27CCCh. 4.13 - Prob. 12LTSCh. 4.13 - Prob. 28PTSCh. 4.13 - Prob. 29ATSCh. 4.13 - Prob. 13LTSCh. 4.13 - Prob. 30PTSCh. 4.13 - Prob. 31ATSCh. 4.13 - Prob. 32ATSCh. 4.14 - Prob. 33CCCh. 4.14 - Prob. 34CCCh. 4.14 - Prob. 35CCCh. 4 - Prob. 36PPCh. 4 - Prob. 37PPCh. 4 - Prob. 38PPCh. 4 - Prob. 39PPCh. 4 - Prob. 40PPCh. 4 - Prob. 41PPCh. 4 - Prob. 42PPCh. 4 - Prob. 43PPCh. 4 - Prob. 44PPCh. 4 - Prob. 45PPCh. 4 - Prob. 46PPCh. 4 - Prob. 47PPCh. 4 - Prob. 48PPCh. 4 - Prob. 49PPCh. 4 - Prob. 50PPCh. 4 - Prob. 51PPCh. 4 - Prob. 52PPCh. 4 - Prob. 53PPCh. 4 - Prob. 54PPCh. 4 - Prob. 55PPCh. 4 - Prob. 56PPCh. 4 - Prob. 57PPCh. 4 - Prob. 58PPCh. 4 - Prob. 59PPCh. 4 - Prob. 60PPCh. 4 - Prob. 61IPCh. 4 - Prob. 62IPCh. 4 - Prob. 64IPCh. 4 - Prob. 65IPCh. 4 - Prob. 66IPCh. 4 - Prob. 67IPCh. 4 - Prob. 68IPCh. 4 - Prob. 69IPCh. 4 - Prob. 70IPCh. 4 - All of the following are representations of...Ch. 4 - Prob. 72IPCh. 4 - Which of the following is expected to have the...Ch. 4 - Prob. 74IPCh. 4 - Prob. 75CPCh. 4 - The all-trans-1,2,3,4,5,6-hexaethylcyclohexane...Ch. 4 - Compounds 1 and 2 were prepared, and the...
Knowledge Booster
Background pattern image
Similar 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