Chemistry: The Molecular Science
5th Edition
ISBN: 9781285199047
Author: John W. Moore, Conrad L. Stanitski
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Textbook Question
Chapter 6, Problem 74QRT
Acrylonitrile is the building block of the synthetic fiber Orlon.
(a) Which carbon-carbon bond is shorter?
(b) Which carbon-carbon bond is stronger?
(c) Which bond is the most polar? What is the partial negative end of that bond?
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
(a) Complete the Lewis structure for vinyl chloride by
showing all unshared pairs of electrons.
(b) Predict the H-C-H, H-C-C, and Cl-C-H
bond angles in this molecule.
(c) Does vinyl chloride have polar bonds? Is it a
polar molecule? Does it have a dipole?
For each of the following covalent bonds: (a) use the symbols δ+ and δ- to indicate the direction of polarity (if any).(a) C-F; (b) N-Br; (c) B-C; (d) Si-H(b) Rank the following covalent bonds in order of increasing polarity. (i) C-H, O-H, N-H; (ii) C-N, C-O, B-O; (iii) C-P, C-S, C-N
Write the Lewis structures for the following, and include resonance structures where appropriate. Indicate which has the strongest carbon-oxygen bond.(a) CO2(b) CO
Chapter 6 Solutions
Chemistry: The Molecular Science
Ch. 6.2 - Write Lewis structures for (a) NF3, (b) N2H4, and...Ch. 6.3 - Prob. 6.1ECh. 6.3 - Prob. 6.2PSPCh. 6.4 - Prob. 6.2CECh. 6.4 - Write Lewis structures for (a) nitrosyl ion, NO+;...Ch. 6.5 - Prob. 6.4CECh. 6.5 - Prob. 6.5CECh. 6.5 - Prob. 6.4PSPCh. 6.6 - Prob. 6.5PSPCh. 6.6 - Use Equation 6.1 and values from Table 6.2 to...
Ch. 6.6 - Prob. 6.6CECh. 6.7 - Prob. 6.7PSPCh. 6.7 - Prob. 6.7CECh. 6.8 - Prob. 6.8PSPCh. 6.9 - Prob. 6.9PSPCh. 6.9 - Prob. 6.9CECh. 6.10 - Prob. 6.10PSPCh. 6.11 - Prob. 6.10ECh. 6.11 - Prob. 6.11ECh. 6.11 - Prob. 1CECh. 6.11 - Prob. 2CECh. 6.12 - Repeat Problem-Solving Example 6.11, but use N2...Ch. 6.12 - Use MO theory to predict the bond order and the...Ch. 6 - Prob. 1QRTCh. 6 - Prob. 2QRTCh. 6 - Prob. 3QRTCh. 6 - Prob. 4QRTCh. 6 - Prob. 5QRTCh. 6 - Prob. 6QRTCh. 6 - Which of these molecules have an odd number of...Ch. 6 - Prob. 8QRTCh. 6 - Prob. 9QRTCh. 6 - Prob. 10QRTCh. 6 - Prob. 11QRTCh. 6 - Prob. 12QRTCh. 6 - Explain in your own words why the energy of two H...Ch. 6 - Prob. 14QRTCh. 6 - Prob. 15QRTCh. 6 - Prob. 16QRTCh. 6 - Prob. 17QRTCh. 6 - Prob. 18QRTCh. 6 - Prob. 19QRTCh. 6 -
Write Lewis structures for
tetracyanoethene,...Ch. 6 - Prob. 21QRTCh. 6 - Prob. 22QRTCh. 6 - Prob. 23QRTCh. 6 - Prob. 24QRTCh. 6 - Prob. 25QRTCh. 6 - Prob. 26QRTCh. 6 - Prob. 27QRTCh. 6 - Prob. 28QRTCh. 6 - Prob. 29QRTCh. 6 - For each pair of bonds, predict which is the...Ch. 6 - Prob. 31QRTCh. 6 - Prob. 32QRTCh. 6 - Which bond requires more energy to break: the...Ch. 6 -
Estimate ΔrH° for forming 2 mol ammonia from...Ch. 6 - Prob. 35QRTCh. 6 - Light of appropriate wavelength can break chemical...Ch. 6 - Prob. 37QRTCh. 6 - Prob. 38QRTCh. 6 - Prob. 39QRTCh. 6 - Acrolein is the starting material for certain...Ch. 6 - Prob. 41QRTCh. 6 - Prob. 42QRTCh. 6 - Write the correct Lewis structure and assign a...Ch. 6 - Prob. 44QRTCh. 6 - Prob. 45QRTCh. 6 - Two Lewis structures can be written for nitrosyl...Ch. 6 - Prob. 47QRTCh. 6 - Prob. 48QRTCh. 6 - Prob. 49QRTCh. 6 - Prob. 50QRTCh. 6 - Several Lewis structures can be written for...Ch. 6 - Prob. 52QRTCh. 6 - Prob. 53QRTCh. 6 - Prob. 54QRTCh. 6 - Prob. 55QRTCh. 6 - Draw resonance structures for each of these ions:...Ch. 6 - Three known isomers exist of N2CO, with the atoms...Ch. 6 - Write the Lewis structure for (a) BrF5 (b) IF5 (c)...Ch. 6 - Write the Lewis structure for
BrF3
XeF4
Ch. 6 - Prob. 60QRTCh. 6 - Prob. 61QRTCh. 6 - Prob. 62QRTCh. 6 - All carbon-to-carbon bond lengths are identical in...Ch. 6 - Prob. 64QRTCh. 6 - Prob. 65QRTCh. 6 - Prob. 66QRTCh. 6 - Prob. 67QRTCh. 6 - Prob. 68QRTCh. 6 - Prob. 69QRTCh. 6 - Prob. 70QRTCh. 6 - Using just a periodic table (not a table of...Ch. 6 - The CBr bond length in CBr4 is 191 pm; the BrBr...Ch. 6 - Prob. 73QRTCh. 6 -
Acrylonitrile is the building block of the...Ch. 6 - Prob. 75QRTCh. 6 - Write Lewis structures for (a) SCl2 (b) Cl3+ (c)...Ch. 6 - Prob. 77QRTCh. 6 - Prob. 78QRTCh. 6 - A student drew this incorrect Lewis structure for...Ch. 6 - This Lewis structure for SF5+ is drawn...Ch. 6 - Tribromide, Br3, and triiodide, I3, ions are often...Ch. 6 - Explain why nonmetal atoms in Period 3 and beyond...Ch. 6 - Prob. 83QRTCh. 6 - Prob. 84QRTCh. 6 - Prob. 85QRTCh. 6 - Prob. 86QRTCh. 6 - Which of these molecules is least likely to exist:...Ch. 6 - Write the Lewis structure for nitrosyl fluoride,...Ch. 6 - Prob. 91QRTCh. 6 - Methylcyanoacrylate is the active ingredient in...Ch. 6 - Aspirin is made from salicylic acid, which has...Ch. 6 - Prob. 94QRTCh. 6 - Prob. 95QRTCh. 6 - Prob. 96QRTCh. 6 - Prob. 97QRTCh. 6 - Prob. 98QRTCh. 6 - Nitrosyl azide, N4O, is a pale yellow solid first...Ch. 6 - Write the Lewis structures for (a) (Cl2PN)3 (b)...Ch. 6 - Nitrous oxide, N2O, is a linear molecule that has...Ch. 6 - The azide ion, N3, has three resonance hybrid...Ch. 6 - Hydrazoic acid, HN3, has three resonance hybrid...Ch. 6 - Prob. 104QRTCh. 6 - Experimental evidence indicates the existence of...Ch. 6 - Prob. 106QRTCh. 6 - Prob. 107QRTCh. 6 - Pipeline, the active ingredient in black pepper,...Ch. 6 - Sulfur and oxygen form a series of 2 anions...Ch. 6 - Prob. 110QRTCh. 6 - Prob. 111QRTCh. 6 - Prob. 112QRTCh. 6 - Prob. 113QRTCh. 6 - Prob. 114QRTCh. 6 - Prob. 115QRTCh. 6 - Prob. 116QRTCh. 6 - Prob. 117QRTCh. 6 - Prob. 118QRTCh. 6 - Prob. 6.ACPCh. 6 - Prob. 6.BCPCh. 6 - Prob. 6.CCP
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
- Write Lewis structures for these compounds. Show all valence electrons. None of them contains a ring of atoms. (a) Hydrogen peroxide, H2O2 (b) Hydrazine, N2H4 (c) Methanol, CH3OHarrow_forwardClassify the following bonds as nonpolar, polar, or ionic: (a) the bond in ClF, (b) the bond in CsBr, and (c) the carbon-carbon double bond in C2H4.arrow_forwarda) Draw the Lewis structure of H3PO4. b) In H3PO4, one P-O bond has a different bond length than the other three. Would it be shorter or longer than the others? Justify your answer.arrow_forward
- Draw the molecules in Problem 1.61 using line structuresarrow_forwardThe arrangement of atoms in several biologically important molecules is given here. Complete the Lewis structures of these molecules by adding multiple bonds and lone pairs. Do not add any more atoms. (a) the amino acid serine: 車 0-H H-C-H H Н—N—с—с—о—н H (b) нон H-N-C-N-H (c) pyruvic acid: ноо н—с—с—с—о—н H. (d) uracil: H (e) carbonic acid: H-0-C-0-Harrow_forwardConsider lisinopril, a drug used primarily in the treatment of high blood pressure, heart failure, and after heart attacks. (a) Complete the Lewis structure of lisinopril, showing all valence electrons. (b) Use the valence-shell electron-pair repulsion (VSEPR) model (Section 3.10) to predict all bond angles in lisinopril. (c) Which is the most polar bond in lisinopril? (d) Is lisinopril polar or nonpolar? (e) Is lisinopril expected to possess resonance (Section 3.9)? Explain why or why not. (f) Name the various functional groups in lisinopril. (g) What is the molecular formula of lisinopril? (h) What intermolecular forces are expected to exist between molecules of lisinopril in close proximity to one another (Section 5.7)?arrow_forward
- Consider lisinopril, a drug used primarily in the treatment of high blood pressure, heart failure, and after heart attacks. (a) Complete the Lewis structure of lisinopril, showing all valence electrons. (b) Use the valence-shell electron-pair repulsion (VSEPR) model (Section 3.10) to predict all bond angles in lisinopril. (c) Which is the most polar bond in lisinopril? (d) Is lisinopril polar or nonpolar? (e) Is lisinopril expected to possess resonance (Section 3.9)? Explain why or why not. (f) Name the various functional groups in lisinopril. (g) What is the molecular formula of lisinopril? (h) What intermolecular forces are expected to exist between molecules of lisinopril in close proximity to one another (Section 5.7)?arrow_forwardWhich statements are true about electronegativity? (a) Electronegativity increases from left to right in a period of the Periodic Table. (b) Electronegativity increases from top to bottom in a column of the Periodic Table . (c) Hydrogen, the element with the lowest atomic number, has the smallest electronegativity. (d) The higher the atomic number of an element, the greater its electronegativity.arrow_forwardThe two compounds nitrogen dioxide and dinitrogen tetraoxide are introduced in Section 3.13. (a) NO2 is an odd-electron compound. Draw the best Lewis diagrams possible for it, recognizing that one atom cannot achieve an octet configuration. Use formal charges to decide whether that should be the (central) nitrogen atom or one of the oxygen atoms. (b) Draw resonance forms for N2O4 that obey the octet rule. The two N atoms are bonded in this molecule.arrow_forward
- Judging from their relative positions in the Periodic Table, which atom in each set is more electronegative? (a) Carbon or nitrogen (b) Chlorine or bromine (c) Oxygen or sulfurarrow_forwardDraw a Lewis structure for each of the following molecules: (a) chlorodifluoromethane, CHClF2 (b) propanoic acid, C2 H5CO2H (basic structure pictured below) (c) acetonitrile, CH3CH (the framework is H3C-C-N) (d) allene, H3CCCH2arrow_forwardDraw Lewis structures for each of the following compounds. In each case, specify the number of valence electrons surrounding the central atom. (Assign lone pairs and radical electrons where appropriate.) (Assume the central atom does not contain an expanded octet.) (a) bromine dioxide (BrO2) (b) beryllium bromide (BeBr2) (c) phosphorus pentafluoride (PF5)arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry by OpenStax (2015-05-04)ChemistryISBN:9781938168390Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark BlaserPublisher:OpenStaxChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningIntroductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning
Chemistry by OpenStax (2015-05-04)
Chemistry
ISBN:9781938168390
Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher:OpenStax
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
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