Chemical Principles: The Quest for Insight
7th Edition
ISBN: 9781464183959
Author: Peter Atkins, Loretta Jones, Leroy Laverman
Publisher: W. H. Freeman
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 2, Problem 2.9E
(a)
Interpretation Introduction
Interpretation:
The Lewis structure of
Concept Introduction:
Lewis structures represent covalent bonds and describe valence electrons configuration of atoms. The covalent bonds are depicted by lines and unshared electron pairs by pairs of dots. The sequence to write Lewis structure of some molecule is given as follows:
- The central atom is identified and various other atoms are arranged around it. This central atom so chosen is often the least electronegative.
- Total valence electrons is estimated.
- single bond is first placed between each atom pair.
- The electrons left can be allocated as unshared electron pairs or as multiple bonds around the
symbol of element to satisfy the octet (or duplet) for each atom. - Add charge on overall structure in case of polytatomic cation or anion.
(b)
Interpretation Introduction
Interpretation:
Lewis structures for benzene with
Concept Introduction:
Refer to part (a).
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Q2: Ranking Acidity
a) Rank the labeled protons in the following molecule in order of increasing pKa. Briefly
explain the ranking. Use Table 2.2 as reference.
Ha
Нь
HC
H-N
Ha
OHe
b) Atenolol is a drug used to treat high blood pressure. Which of the indicated N-H bonds is
more acidic? Explain. (Hint: use resonance structures to help)
Name the functional groups on atenolol.
H
H-N
atenolol
Ν
H-N
OH Н
Answer d, e, and f
If the rotational constant of a molecule is B = 120 cm-1, it can be stated that the transition from 2←1:a) gives rise to a line at 120 cm-1b) is a forbidden transitionc) gives rise to a line at 240 cm-1d) gives rise to a line at 480 cm-1
Chapter 2 Solutions
Chemical Principles: The Quest for Insight
Ch. 2 - Prob. 2A.1ASTCh. 2 - Prob. 2A.1BSTCh. 2 - Prob. 2A.2ASTCh. 2 - Prob. 2A.2BSTCh. 2 - Prob. 2A.3ASTCh. 2 - Prob. 2A.3BSTCh. 2 - Prob. 2A.4ASTCh. 2 - Prob. 2A.4BSTCh. 2 - Prob. 2A.1ECh. 2 - Prob. 2A.2E
Ch. 2 - Prob. 2A.3ECh. 2 - Prob. 2A.4ECh. 2 - Prob. 2A.5ECh. 2 - Prob. 2A.6ECh. 2 - Prob. 2A.7ECh. 2 - Prob. 2A.8ECh. 2 - Prob. 2A.9ECh. 2 - Prob. 2A.10ECh. 2 - Prob. 2A.11ECh. 2 - Prob. 2A.12ECh. 2 - Prob. 2A.13ECh. 2 - Prob. 2A.14ECh. 2 - Prob. 2A.15ECh. 2 - Prob. 2A.16ECh. 2 - Prob. 2A.17ECh. 2 - Prob. 2A.18ECh. 2 - Prob. 2A.19ECh. 2 - Prob. 2A.20ECh. 2 - Prob. 2A.21ECh. 2 - Prob. 2A.22ECh. 2 - Prob. 2A.23ECh. 2 - Prob. 2A.24ECh. 2 - Prob. 2A.25ECh. 2 - Prob. 2A.26ECh. 2 - Prob. 2A.27ECh. 2 - Prob. 2A.28ECh. 2 - Prob. 2A.29ECh. 2 - Prob. 2A.30ECh. 2 - Prob. 2B.1ASTCh. 2 - Prob. 2B.1BSTCh. 2 - Prob. 2B.2ASTCh. 2 - Prob. 2B.2BSTCh. 2 - Prob. 2B.3ASTCh. 2 - Prob. 2B.3BSTCh. 2 - Prob. 2B.4ASTCh. 2 - Prob. 2B.4BSTCh. 2 - Prob. 2B.5ASTCh. 2 - Prob. 2B.5BSTCh. 2 - Prob. 2B.1ECh. 2 - Prob. 2B.2ECh. 2 - Prob. 2B.3ECh. 2 - Prob. 2B.4ECh. 2 - Prob. 2B.5ECh. 2 - Prob. 2B.6ECh. 2 - Prob. 2B.7ECh. 2 - Prob. 2B.8ECh. 2 - Prob. 2B.9ECh. 2 - Prob. 2B.10ECh. 2 - Prob. 2B.11ECh. 2 - Prob. 2B.12ECh. 2 - Prob. 2B.13ECh. 2 - Prob. 2B.14ECh. 2 - Prob. 2B.15ECh. 2 - Prob. 2B.16ECh. 2 - Prob. 2B.17ECh. 2 - Prob. 2B.18ECh. 2 - Prob. 2B.19ECh. 2 - Prob. 2B.20ECh. 2 - Prob. 2B.21ECh. 2 - Prob. 2B.22ECh. 2 - Prob. 2B.23ECh. 2 - Prob. 2B.24ECh. 2 - Prob. 2C.1ASTCh. 2 - Prob. 2C.1BSTCh. 2 - Prob. 2C.2ASTCh. 2 - Prob. 2C.2BSTCh. 2 - Prob. 2C.3ASTCh. 2 - Prob. 2C.3BSTCh. 2 - Prob. 2C.1ECh. 2 - Prob. 2C.2ECh. 2 - Prob. 2C.3ECh. 2 - Prob. 2C.4ECh. 2 - Prob. 2C.5ECh. 2 - Prob. 2C.6ECh. 2 - Prob. 2C.7ECh. 2 - Prob. 2C.8ECh. 2 - Prob. 2C.9ECh. 2 - Prob. 2C.10ECh. 2 - Prob. 2C.11ECh. 2 - Prob. 2C.12ECh. 2 - Prob. 2C.13ECh. 2 - Prob. 2C.14ECh. 2 - Prob. 2C.15ECh. 2 - Prob. 2C.16ECh. 2 - Prob. 2C.17ECh. 2 - Prob. 2C.18ECh. 2 - Prob. 2D.1ASTCh. 2 - Prob. 2D.1BSTCh. 2 - Prob. 2D.2ASTCh. 2 - Prob. 2D.2BSTCh. 2 - Prob. 2D.1ECh. 2 - Prob. 2D.2ECh. 2 - Prob. 2D.3ECh. 2 - Prob. 2D.4ECh. 2 - Prob. 2D.5ECh. 2 - Prob. 2D.6ECh. 2 - Prob. 2D.7ECh. 2 - Prob. 2D.8ECh. 2 - Prob. 2D.9ECh. 2 - Prob. 2D.10ECh. 2 - Prob. 2D.11ECh. 2 - Prob. 2D.12ECh. 2 - Prob. 2D.13ECh. 2 - Prob. 2D.14ECh. 2 - Prob. 2D.15ECh. 2 - Prob. 2D.16ECh. 2 - Prob. 2D.17ECh. 2 - Prob. 2D.18ECh. 2 - Prob. 2D.19ECh. 2 - Prob. 2D.20ECh. 2 - Prob. 2E.1ASTCh. 2 - Prob. 2E.1BSTCh. 2 - Prob. 2E.2ASTCh. 2 - Prob. 2E.2BSTCh. 2 - Prob. 2E.3ASTCh. 2 - Prob. 2E.3BSTCh. 2 - Prob. 2E.4ASTCh. 2 - Prob. 2E.4BSTCh. 2 - Prob. 2E.5ASTCh. 2 - Prob. 2E.5BSTCh. 2 - Prob. 2E.1ECh. 2 - Prob. 2E.2ECh. 2 - Prob. 2E.3ECh. 2 - Prob. 2E.4ECh. 2 - Prob. 2E.5ECh. 2 - Prob. 2E.6ECh. 2 - Prob. 2E.7ECh. 2 - Prob. 2E.8ECh. 2 - Prob. 2E.9ECh. 2 - Prob. 2E.10ECh. 2 - Prob. 2E.11ECh. 2 - Prob. 2E.12ECh. 2 - Prob. 2E.13ECh. 2 - Prob. 2E.14ECh. 2 - Prob. 2E.15ECh. 2 - Prob. 2E.16ECh. 2 - Prob. 2E.17ECh. 2 - Prob. 2E.18ECh. 2 - Prob. 2E.19ECh. 2 - Prob. 2E.20ECh. 2 - Prob. 2E.21ECh. 2 - Prob. 2E.22ECh. 2 - Prob. 2E.23ECh. 2 - Prob. 2E.24ECh. 2 - Prob. 2E.25ECh. 2 - Prob. 2E.26ECh. 2 - Prob. 2E.27ECh. 2 - Prob. 2E.28ECh. 2 - Prob. 2E.29ECh. 2 - Prob. 2E.30ECh. 2 - Prob. 2F.1ASTCh. 2 - Prob. 2F.1BSTCh. 2 - Prob. 2F.2ASTCh. 2 - Prob. 2F.2BSTCh. 2 - Prob. 2F.3ASTCh. 2 - Prob. 2F.3BSTCh. 2 - Prob. 2F.4ASTCh. 2 - Prob. 2F.4BSTCh. 2 - Prob. 2F.1ECh. 2 - Prob. 2F.2ECh. 2 - Prob. 2F.3ECh. 2 - Prob. 2F.4ECh. 2 - Prob. 2F.5ECh. 2 - Prob. 2F.6ECh. 2 - Prob. 2F.7ECh. 2 - Prob. 2F.8ECh. 2 - Prob. 2F.9ECh. 2 - Prob. 2F.10ECh. 2 - Prob. 2F.11ECh. 2 - Prob. 2F.12ECh. 2 - Prob. 2F.13ECh. 2 - Prob. 2F.14ECh. 2 - Prob. 2F.15ECh. 2 - Prob. 2F.16ECh. 2 - Prob. 2F.17ECh. 2 - Prob. 2F.18ECh. 2 - Prob. 2F.19ECh. 2 - Prob. 2F.20ECh. 2 - Prob. 2F.21ECh. 2 - Prob. 2G.1ASTCh. 2 - Prob. 2G.1BSTCh. 2 - Prob. 2G.2ASTCh. 2 - Prob. 2G.2BSTCh. 2 - Prob. 2G.1ECh. 2 - Prob. 2G.2ECh. 2 - Prob. 2G.3ECh. 2 - Prob. 2G.4ECh. 2 - Prob. 2G.5ECh. 2 - Prob. 2G.6ECh. 2 - Prob. 2G.7ECh. 2 - Prob. 2G.8ECh. 2 - Prob. 2G.9ECh. 2 - Prob. 2G.11ECh. 2 - Prob. 2G.12ECh. 2 - Prob. 2G.13ECh. 2 - Prob. 2G.14ECh. 2 - Prob. 2G.15ECh. 2 - Prob. 2G.16ECh. 2 - Prob. 2G.17ECh. 2 - Prob. 2G.18ECh. 2 - Prob. 2G.19ECh. 2 - Prob. 2G.20ECh. 2 - Prob. 2G.21ECh. 2 - Prob. 2G.22ECh. 2 - Prob. 2.1ECh. 2 - Prob. 2.2ECh. 2 - Prob. 2.3ECh. 2 - Prob. 2.4ECh. 2 - Prob. 2.5ECh. 2 - Prob. 2.6ECh. 2 - Prob. 2.7ECh. 2 - Prob. 2.8ECh. 2 - Prob. 2.9ECh. 2 - Prob. 2.10ECh. 2 - Prob. 2.11ECh. 2 - Prob. 2.12ECh. 2 - Prob. 2.13ECh. 2 - Prob. 2.14ECh. 2 - Prob. 2.17ECh. 2 - Prob. 2.19ECh. 2 - Prob. 2.22ECh. 2 - Prob. 2.23ECh. 2 - Prob. 2.24ECh. 2 - Prob. 2.25ECh. 2 - Prob. 2.26ECh. 2 - Prob. 2.27ECh. 2 - Prob. 2.28ECh. 2 - Prob. 2.29ECh. 2 - Prob. 2.30ECh. 2 - Prob. 2.31ECh. 2 - Prob. 2.32ECh. 2 - Prob. 2.33ECh. 2 - Prob. 2.34ECh. 2 - Prob. 2.35ECh. 2 - Prob. 2.36ECh. 2 - Prob. 2.37ECh. 2 - Prob. 2.39ECh. 2 - Prob. 2.40ECh. 2 - Prob. 2.41ECh. 2 - Prob. 2.42ECh. 2 - Prob. 2.43ECh. 2 - Prob. 2.44ECh. 2 - Prob. 2.45ECh. 2 - Prob. 2.46ECh. 2 - Prob. 2.47ECh. 2 - Prob. 2.48ECh. 2 - Prob. 2.49ECh. 2 - Prob. 2.50ECh. 2 - Prob. 2.51ECh. 2 - Prob. 2.52ECh. 2 - Prob. 2.53ECh. 2 - Prob. 2.54ECh. 2 - Prob. 2.55ECh. 2 - Prob. 2.56ECh. 2 - Prob. 2.57ECh. 2 - Prob. 2.58ECh. 2 - Prob. 2.59ECh. 2 - Prob. 2.60ECh. 2 - Prob. 2.61ECh. 2 - Prob. 2.62ECh. 2 - Prob. 2.63ECh. 2 - Prob. 2.64E
Knowledge Booster
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
- Briefly indicate the coordination forms of B and Si in borates and silicates, respectively.arrow_forwardCan you please draw out the Lewis structure for these two formulasarrow_forwardIn a rotational Raman spectrum of a diatomic molecule it is correct to say that:a) anti-Stokes lines occur at frequencies higher than the excitatory oneb) Stokes lines occur at frequencies higher than the excitatory onec) Rayleigh scattering is not observedd) Rayleigh scattering corresponds to delta J = 0arrow_forward
- Of the molecules: H2, N2, HCl, CO2, indicate which ones can give Raman vibration-rotation spectra:a) H2, N2 and HClb) H2, N2, HCl and CO2c) H2 and N2d) all of themarrow_forwardCan you please help me with drawing the Lewis structure of each molecular formula?I truly appreciate you!arrow_forwardCan you please help me with drawing the Lewis structure of each molecular formula?I truly appreciate you!arrow_forward
- Describe each highlighted bond in terms of the overlap of atomic orbitals. (a) Н Н H H [References] HIC H H C H H-C-CC-N: H σ character n character (b) HIC H H H H-C-C-C HIC H Н H O-H σ character n character Submit Answer Try Another Version 3 item attempts remainingarrow_forward11 Naming and drawing alcohols Write the systematic (IUPAC) name for each of the following organic molecules: structure OH HO OH Explanation Check name ☐arrow_forwardwhat is the drawn mechanism for diethyl carbonate and 4 - bromo - N, N -dimethylaniline to create crystal violet?arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- General Chemistry - Standalone book (MindTap Cour...ChemistryISBN:9781305580343Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; DarrellPublisher:Cengage LearningGeneral, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
General Chemistry - Standalone book (MindTap Cour...
Chemistry
ISBN:9781305580343
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Publisher:Cengage Learning
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
Stoichiometry - Chemistry for Massive Creatures: Crash Course Chemistry #6; Author: Crash Course;https://www.youtube.com/watch?v=UL1jmJaUkaQ;License: Standard YouTube License, CC-BY
Bonding (Ionic, Covalent & Metallic) - GCSE Chemistry; Author: Science Shorts;https://www.youtube.com/watch?v=p9MA6Od-zBA;License: Standard YouTube License, CC-BY
General Chemistry 1A. Lecture 12. Two Theories of Bonding.; Author: UCI Open;https://www.youtube.com/watch?v=dLTlL9Z1bh0;License: CC-BY