CHEMICAL PRINCIPLES (LL) W/ACCESS
7th Edition
ISBN: 9781319421175
Author: ATKINS
Publisher: MAC HIGHER
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 2, Problem 2B.13E
Interpretation Introduction
Interpretation:
The structure of anthracene has to be completed with multiple bonds to satisfy the octet rule at each carbon atom and possible resonance structures have to be drawn.
Concept Introduction:
When a single Lewis structure cannot describe all the experimentally observed properties of a molecule more than one Lewis structure that differs only in position of multiple bonds is drawn. These are termed resonance structures. The actual molecule is represented by the hybrid of each of these resonance structures. For example, for molecule like ozone
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionChapter 2 Solutions
CHEMICAL PRINCIPLES (LL) W/ACCESS
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
- Experimental evidence indicates the existence of HC3N molecules in interstellar clouds. Write a plausible Lewis structure for this molecule.arrow_forwardFormamide, HC(O)NH2, is prepared at high pressures from carbon monoxide and ammonia, and serves as an industrial solvent (the parentheses around the O indicate that it is bonded only to the carbon atom and that the carbon atom is also bonded to the H and the N atoms). Two resonance forms (one with formal charges) can be written for formamide. Write both resonance structures, and predict the bond angles about the carbon and nitrogen atoms for each resonance form. Are they the same? Describe how the experimental determination of the HNH bond angle could be used to indicate which resonance form is more important.arrow_forwardBond Enthalpy When atoms of the hypothetical element X are placed together, they rapidly undergo reaction to form the X2 molecule: X(g)+X(g)X2(g) a Would you predict that this reaction is exothermic or endothermic? Explain. b Is the bond enthalpy of X2 a positive or a negative quantity? Why? c Suppose H for the reaction is 500 kJ/mol. Estimate the bond enthalpy of the X2 molecule. d Another hypothetical molecular compound, Y2(g), has a bond enthalpy of 750 kJ/mol, and the molecular compound XY(g) has a bond enthalpy of 1500 kJ/mol. Using bond enthalpy information, calculate H for the following reaction. X2(g)+Y2(g)2XY(g) e Given the following information, as well as the information previously presented, predict whether or not the hypothetical ionic compound AX is likely to form. In this compound, A forms the A+ cation, and X forms the X anion. Be sure to justify your answer. Reaction: A(g)+12X2(g)AX(s)The first ionization energy of A(g) is 400 kJ/mol. The electron affinity of X(g) is 525 kJ/mol. The lattice energy of AX(s) is 100 kJ/mol. f If you predicted that no ionic compound would form from the reaction in Part e, what minimum amount of AX(s) lattice energy might lead to compound formation?arrow_forward
- Draw Lewis structures for the following species. (The skeleton is indicated by the way the molecule is written.) (a) Cl2CO (b) H3C—CN (c) H2C—CH2arrow_forwardConsider the following compounds: CO2, SO2, KrF2, SO3, NF3, IF3, CF4, SF4, XeF4, PF5, TF5, and SCl6. These 12 compounds are all examples of different molecular structures. Draw the Lewis structures for each and predict the molecular structures. Predict the bond angles and the polarity of each. (A polar molecule has a net dipole moment, while a nonpolar molecule does not.) See Exercises 25 and 26 for the molecular structures based on the trigonal bipyramid and the octahedral geometries.arrow_forwardChloromethane has the Lewis structure _______________________________ The carbon atom is sharing 4 electron pairs. In each shared pair the carbon atom “owns” 1 electron. The number of electrons that “belong” to carbon is ___. Carbon, being a Group ___ element would have 4 , outer shell electrons in the unbonded, neutral state. Therefore, the carbon atom in chloromethane has a formal charge of zero.arrow_forward
- Two different molecules have the formula C2H6O. One of the molecules has the oxygen atom bonded to both carbon atoms. The other molecule has the oxygen atom bonded to only one carbon atom while both carbon atoms are bonded to each other. Write Lewis structures for both of these compounds.arrow_forwardWrite all resonance structures of chlorobenzene, C6H5Cl, a molecule with the same cyclic structure as benzene. In all structures, keep the CCl bond as a single bond. Which resonance structures are the most important?arrow_forwardMethylcyanoacrylate is the active ingredient in super glues. Its Lewis structure is In this molecule, which is the (a) weakest carbon-containing bond? (b) strongest carbon-containing bond? (c) most polar bond?arrow_forward
- Write the Lewis structure for nitrosyl fluoride, FNO. Using only a periodic table, identify (a) which is the longer bond. (b) which is the stronger bond. (c) which is the more polar bond.arrow_forwardConsider the pyrosulfate ion, S2O72-. It has no sulfur–sulfur nor oxygen–oxygen bonds. (a) Write a Lewis structure for the pyrosulfate ion using only single bonds. (b) What is the formal charge on the sulfur atoms for the Lewis structure you drew in part (a)? (c) Write another Lewis structure using six bonds and two O—S bonds. (d) What is the formal charge on each atom for the structure you drew in part (c)?arrow_forward3. The skeleton of chloromethane is __________________ The central carbon atom is bonded to each of the other atoms by a shared electron pair (represented by a straight line, ___) giving Now, each hydrogen has two electrons and the carbon atom has eight. However, chlorine must be provided with unshared electrons (represented by pairs of dots, ) to complete its octet, thusarrow_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 Learning
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage LearningChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher: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
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning