Chemistry
7th Edition
ISBN: 9780321940872
Author: John E. McMurry, Robert C. Fay, Jill Kirsten Robinson
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 7, Problem 7.1P
Interpretation Introduction
To determine:
Type of compound.
Expert Solution & Answer
Answer to Problem 7.1P
- Nonpolar covalent
- Ionic
- Ionic
- Nonpolar covalent
Explanation of Solution
Recall that the nature of the compound will depend on the electronegativity differences between the species involved. If the electronegativity difference between the atoms is large enough, it will be ionic, that is, this is not a shared bond, rather a donation/acceptance of electron. This is called ionic bonding since the cation and anion will interact via electrostatic forces. These are CsBr, which is metal and nonmetal bond, and FeBr3, which is once again metal with nonmetal. These will typically form ionic bonding.
Covalent bonding forced when species are not that different in electronegativity. They are bonded due to the sharing of electrons. There might be uneven sharing of electrons, and there could be a polar molecule formation, or there could be even sharing of electrons, which causes a pure nonpolar covalent compound.
Methane, CH4, is a nonpolar covalent compound, due to its symmetry. Then comes SiCl4, which is similar to methane, in which the hydrogen atoms are both bonded to a central atom. It is also nonpolar covalent.
Conclusion
The nature of polar and ionic bonding depends mainly on the electronegativity difference of the species.
Want to see more full solutions like this?
Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
Provide the complete mechanism for the reactions below. You must include appropriate arrows,intermediates, and formal charges.
Indicate the products obtained by reacting fluorobenzene with a sulfonitric mixture.
If I have 1-bromopropene, to obtain compound
A, I have to add NaOH and another compound.
Indicate which compound that would be.
C6H5 CH3
Chapter 7 Solutions
Chemistry
Ch. 7 - Prob. 7.1PCh. 7 - Conceptual APPLY 7.2 An electrostatic potential...Ch. 7 - Prob. 7.3PCh. 7 - Prob. 7.4ACh. 7 - Prob. 7.5PCh. 7 - Prob. 7.6ACh. 7 - Prob. 7.7PCh. 7 - Prob. 7.8ACh. 7 - Prob. 7.9PCh. 7 - Prob. 7.10A
Ch. 7 - Prob. 7.11PCh. 7 - Prob. 7.12ACh. 7 - Prob. 7.13PCh. 7 - Prob. 7.14ACh. 7 - Prob. 7.15PCh. 7 - Prob. 7.16ACh. 7 - Prob. 7.17PCh. 7 - Prob. 7.18ACh. 7 - Prob. 7.19PCh. 7 - Prob. 7.20ACh. 7 - Prob. 7.21PCh. 7 - Prob. 7.22ACh. 7 - Prob. 7.23PCh. 7 - Prob. 7.24PCh. 7 - Prob. 7.25PCh. 7 - Prob. 7.26PCh. 7 - Prob. 7.27PCh. 7 - Prob. 7.28PCh. 7 - Prob. 7.29CPCh. 7 - Prob. 7.30CPCh. 7 - Prob. 7.31CPCh. 7 - Prob. 7.32CPCh. 7 - Prob. 7.33CPCh. 7 - Prob. 7.34CPCh. 7 - Prob. 7.35CPCh. 7 - Prob. 7.36CPCh. 7 - Prob. 7.37CPCh. 7 - Prob. 7.38CPCh. 7 - Prob. 7.39CPCh. 7 - Prob. 7.40CPCh. 7 - Prob. 7.41CPCh. 7 - Prob. 7.42CPCh. 7 - Prob. 7.43CPCh. 7 - Prob. 7.44CPCh. 7 - Prob. 7.45CPCh. 7 - Prob. 7.46CPCh. 7 - Prob. 7.47CPCh. 7 - Prob. 7.48CPCh. 7 - Which of the substances...Ch. 7 - Prob. 7.50CPCh. 7 - Order the following compounds according to the...Ch. 7 - Prob. 7.52CPCh. 7 - Prob. 7.53CPCh. 7 - Prob. 7.54CPCh. 7 - Prob. 7.55CPCh. 7 - Explain the difference in the bond dissociation...Ch. 7 - Explain the difference in the bond dissociation...Ch. 7 - Prob. 7.58CPCh. 7 - Prob. 7.59CPCh. 7 - Prob. 7.60CPCh. 7 - Prob. 7.61CPCh. 7 - Prob. 7.62CPCh. 7 - Prob. 7.63CPCh. 7 - Prob. 7.64CPCh. 7 - Prob. 7.65CPCh. 7 - Prob. 7.66CPCh. 7 - Prob. 7.67CPCh. 7 - Prob. 7.68CPCh. 7 - Prob. 7.69CPCh. 7 - Prob. 7.70CPCh. 7 - Prob. 7.71CPCh. 7 - Identify the third-row elements, X, that form the...Ch. 7 - Identify the fourth-row elements, X, that form the...Ch. 7 - Prob. 7.74CPCh. 7 - Prob. 7.75CPCh. 7 - Methyiphenidat (C14H19NO2) , marketed as Ritalin,...Ch. 7 - Prob. 7.77CPCh. 7 - Prob. 7.78CPCh. 7 - Prob. 7.79CPCh. 7 - Prob. 7.80CPCh. 7 - Prob. 7.81CPCh. 7 - Prob. 7.82CPCh. 7 - Prob. 7.83CPCh. 7 - Prob. 7.84CPCh. 7 - Prob. 7.85CPCh. 7 - Prob. 7.86CPCh. 7 - Prob. 7.87CPCh. 7 - Prob. 7.88CPCh. 7 - Prob. 7.89CPCh. 7 - Prob. 7.90CPCh. 7 - Draw two electron-dot resonance structures that...Ch. 7 - Prob. 7.92CPCh. 7 - Prob. 7.93CPCh. 7 - Prob. 7.94CPCh. 7 - Prob. 7.95CPCh. 7 - Prob. 7.96CPCh. 7 - Prob. 7.97CPCh. 7 - Prob. 7.98CPCh. 7 - Prob. 7.99CPCh. 7 - Write an electron-dot structure for chloral...Ch. 7 - Prob. 7.101CPCh. 7 - Prob. 7.102CPCh. 7 - Prob. 7.103CPCh. 7 - Prob. 7.104CPCh. 7 - Prob. 7.105CPCh. 7 - 7.106 Themolecule has nitrogen-oxygen bonds, but...Ch. 7 - Prob. 7.107CPCh. 7 - Prob. 7.108MPCh. 7 - Prob. 7.109MPCh. 7 - Prob. 7.110MPCh. 7 - Prob. 7.111MPCh. 7 - Prob. 7.112MP
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
- If I have 1-bromopropene and I want to obtain (1,1-dipropoxyethyl)benzene, indicate the compound that I should add in addition to NaOH.arrow_forwardDraw the major product of this reaction. Ignore inorganic byproducts. Ο HSCH2CH2CH2SH, BF3 Select to Draw I Submitarrow_forwardFeedback (7/10) Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. Incorrect, 3 attempts remaining Ο (CH3CH2)2NH, TSOH Select to Draw V N. 87% Retryarrow_forward
- If I want to obtain (1,1-dipropoxyethyl)benzene from 1-bromopropene, indicate the product that I have to add in addition to NaOH.arrow_forwardIndicate the products obtained when fluorobenzene reacts with a sulfonitric acid mixture (HNO3 + H2SO4). Indicate the majority if necessary.arrow_forwardIndicate the products obtained when chlorobenzene acid reacts with a sulfonitric acid mixture (HNO3 + H2SO4). Indicate the majority if necessary.arrow_forward
- Indicate the products obtained by reacting benzenesulfonic acid with a sulfonitric acid mixture (HNO3 + H2SO4). Indicate the majority if necessary.arrow_forwardIndicate the products obtained by reacting ethylbenzene with a sulfonitric acid mixture (HNO3 + H2SO4). Indicate the majority if necessary.arrow_forwardIndicate the products obtained when tert-butylbenzene reacts with a sulfonitric acid mixture (HNO3 + H2SO4). Indicate the majority if necessary.arrow_forward
- Indicate the products obtained when acetophenone reacts with a sulfonitric acid mixture (HNO3 + H2SO4). Indicate the majority if necessary.arrow_forwardIndicate the products obtained from the reaction of N-(4-methylphenyl)acetamide with a sulfonitric acid mixture (H2SO4 + HNO3). Indicate the majority if necessary.arrow_forwardIndicate the products obtained from the reaction of 4-(trifluoromethyl)benzonitrile with a sulfonitric mixture (H2SO4 + HNO3). Indicate the majority if necessary.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
ChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill Education
Principles of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill Education
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY
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