Chemistry: An Atoms First Approach
Chemistry: An Atoms First Approach
2nd Edition
ISBN: 9781305079243
Author: Steven S. Zumdahl, Susan A. Zumdahl
Publisher: Cengage Learning
bartleby

Concept explainers

Question
Book Icon
Chapter 19, Problem 46E
Interpretation Introduction

Interpretation: The comparison of the Lewis structures with the molecular orbital view of the bonding in NO, NO+ and NO- is to be done.  Discrepancies between the two models if present are to be accounted.

Concept introduction: When the atomic orbitals overlap with each other in the region where density of electrons is high, then molecular orbitals are formed.  Overlap of the atomic orbitals determines the efficiency of the interaction between the atomic orbitals.

Energy of bonding molecular orbitals is less than the nonbonding molecular orbitals.

To determine: The comparison of the Lewis structures with the molecular orbital view of the bonding in NO, NO+ and NO-.

Blurred answer
Students have asked these similar questions
the three stable oxides of carbon monoxide (CO), Carbon dioxide(CO2), and carbon suboxide (C3O2). for each oxide draw the Lewis structure, predict the molecular structure, and described the bonding in terms of the hybrid orbitals for carbon atoms.
CO, CO₂, CH3OH, and CO32- all contain carbon-oxygen bonds. Draw Lewis structures for these molecules and ions. Given that double bonds are stronger than single bonds and triple bonds are stronger than double bonds, rank the four species in order of increasing CO bond strength. Weakest: Strongest:
When considering the Lewis structure for HF, we might mistakenly conclude that HF contains three lone pairs on the F atom which are degenerate. Explain the nature of these three electron pairs by referring to the molecular orbital energy level diagram.

Chapter 19 Solutions

Chemistry: An Atoms First Approach

Ch. 19 - Prob. 1QCh. 19 - Prob. 2QCh. 19 - Prob. 3QCh. 19 - Diagonal relationships in the periodic table exist...Ch. 19 - Prob. 5QCh. 19 - Prob. 6QCh. 19 - Prob. 7QCh. 19 - Prob. 8QCh. 19 - Prob. 9QCh. 19 - Prob. 10QCh. 19 - Prob. 11ECh. 19 - Prob. 12ECh. 19 - Prob. 13ECh. 19 - Prob. 14ECh. 19 - Prob. 15ECh. 19 - Prob. 16ECh. 19 - Prob. 17ECh. 19 - Prob. 18ECh. 19 - Prob. 19ECh. 19 - Prob. 20ECh. 19 - Prob. 21ECh. 19 - Prob. 22ECh. 19 - Prob. 23ECh. 19 - Prob. 24ECh. 19 - Consider element 113. What is the expected...Ch. 19 - Prob. 26ECh. 19 - Prob. 27ECh. 19 - Prob. 28ECh. 19 - Prob. 29ECh. 19 - Prob. 30ECh. 19 - Prob. 31ECh. 19 - Prob. 32ECh. 19 - Prob. 33ECh. 19 - Prob. 34ECh. 19 - The following illustration shows the orbitals used...Ch. 19 - Prob. 36ECh. 19 - Silicon is produced for the chemical and...Ch. 19 - Prob. 38ECh. 19 - Prob. 39ECh. 19 - Prob. 40ECh. 19 - Prob. 41ECh. 19 - Prob. 42ECh. 19 - Prob. 43ECh. 19 - Prob. 44ECh. 19 - Prob. 45ECh. 19 - Prob. 46ECh. 19 - Prob. 47ECh. 19 - Prob. 48ECh. 19 - Prob. 49ECh. 19 - Prob. 50ECh. 19 - Prob. 51ECh. 19 - Prob. 52ECh. 19 - Use bond energies to estimate the maximum...Ch. 19 - Prob. 54ECh. 19 - Prob. 55ECh. 19 - Prob. 56ECh. 19 - Prob. 57ECh. 19 - Prob. 58ECh. 19 - Prob. 59ECh. 19 - Describe the bonding in SO2 and SO3 using the...Ch. 19 - Prob. 61ECh. 19 - Prob. 62ECh. 19 - Prob. 63ECh. 19 - Prob. 64ECh. 19 - Prob. 65ECh. 19 - Prob. 66ECh. 19 - Prob. 67ECh. 19 - Prob. 68ECh. 19 - Prob. 69ECh. 19 - Prob. 70ECh. 19 - Prob. 71ECh. 19 - Prob. 72ECh. 19 - Prob. 73AECh. 19 - The inert-pair effect is sometimes used to explain...Ch. 19 - Prob. 75AECh. 19 - Prob. 76AECh. 19 - Prob. 77AECh. 19 - Prob. 78AECh. 19 - Prob. 79AECh. 19 - Draw Lewis structures for the AsCl4+ and AsCl6...Ch. 19 - Prob. 81AECh. 19 - Prob. 82AECh. 19 - Prob. 83AECh. 19 - Prob. 84AECh. 19 - Prob. 85AECh. 19 - Prob. 86AECh. 19 - Prob. 87CWPCh. 19 - Prob. 88CWPCh. 19 - Prob. 89CWPCh. 19 - Prob. 90CWPCh. 19 - What is the hybridization of the underlined...Ch. 19 - Prob. 92CWPCh. 19 - What is the hybridization of the central atom in...Ch. 19 - Prob. 94CWPCh. 19 - Prob. 95CWPCh. 19 - Prob. 96CWPCh. 19 - Prob. 97CPCh. 19 - Prob. 98CPCh. 19 - Prob. 99CPCh. 19 - Prob. 100CPCh. 19 - Prob. 101CPCh. 19 - Prob. 102CPCh. 19 - Prob. 103CPCh. 19 - Prob. 104CPCh. 19 - Prob. 105CPCh. 19 - Prob. 106IPCh. 19 - Prob. 107IPCh. 19 - Prob. 108IPCh. 19 - Prob. 109IPCh. 19 - Prob. 110MPCh. 19 - Prob. 111MP
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: Principles and Practice
    Chemistry
    ISBN:9780534420123
    Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
    Publisher:Cengage Learning
    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:9781133611097
    Author:Steven S. Zumdahl
    Publisher:Cengage Learning
  • Text book image
    Chemistry: An Atoms First Approach
    Chemistry
    ISBN:9781305079243
    Author:Steven S. Zumdahl, Susan A. Zumdahl
    Publisher:Cengage Learning
Text book image
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
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:9781133611097
Author:Steven S. Zumdahl
Publisher:Cengage Learning
Text book image
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning