Concept explainers
(a)
Interpretation:
The Lewis structure for formic acid has to be written.
Concept Introduction:
Lewis structure is also known as Lewis dot diagrams or electron dot structures. The bond between atoms and lone pairs of electrons that is present in the molecule. Lewis structure represents each atom and their position in structure using the chemical symbol. Excess electrons forms the lone pair are given by pair of dots, and are located next to the atom.
(b)
Interpretation:
The Lewis structure for Acetonitrile has to be written.
Concept Introduction:
Refer part (a).
(c)
Interpretation:
The Lewis structure for vinyl chloride has to be written.
Concept Introduction:
Refer part (a).
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Chapter 6 Solutions
OWLv2 for Moore/Stanitski's Chemistry: The Molecular Science, 5th Edition, [Instant Access], 1 term (6 months)
- A stable triatomic molecule can be formed that contains one atom each of nitrogen, sulfur, and fluorine. Three bonding structures are possible, depending on which is the central atom: NSF, SNF, and SFN. (a) Write a Lewis diagram for each of these molecules, indicating the formal charge on each atom. (b) Often, the structure with the least separation of formal charge is the most stable. Is this statement consistent with the observed structure for this molecule— namely, NSF, which has a central sulfur atom? (c) Does consideration of the electronegativities of N, S, and F from Figure 3.18 help rationalize this observed structure? Explain. 100. The gasarrow_forwardConsider the formate ion, HCO2", which is the anion formed when formic acid loses an H* ion. The H and the two O atoms are bonded to the central C atom. (a) Draw the best Lewis structure(s) for this ion. (b) Are resonance structures needed to describe the structure? Explain briefly (c) Would you predict that the C-O bond lengths in the formate ion would be longer or shorter relative to those in CO2? Explain brieflyarrow_forwardA resident expert on electronegativity comes up to visit with you. He makes two claims (seen below) about electronegativity with relation to covalent bonding. Is the expert correct or can you refute him with your knowledge of electronegativity? (a) If a diatomic molecule is made up of atoms X and Y, which have different electronegativities, the molecule must be polar. (b) The farther two atoms are apart in a bond, the larger the dipole moment will be.arrow_forward
- (b) Methyl azide, CH-N3 is a molecule that decomposes explosively. Draw a Lewis structure for CH3N3, showing formal charges and also sketch any possible resonance forms.arrow_forwardIn the vapor phase, BeCl2 exists as a discrete molecule. (a) Draw the Lewis structure of this molecule, using only single bonds. Does this Lewis structure satisfy the octet rule? (b) What other resonance structures are possible that satisfy the octet rule? (c) On the basis of the formal charges, which Lewis structure is expected to be dominant for BeCl2?arrow_forwardUse Lewis electron-dot symbols to represent the formationof (a) BrF₃ from bromine and fluorine atoms; (b) AlF₃ from alu-minum and fluorine atoms.arrow_forward
- (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?arrow_forwardWrite Lewis structures for the following: (c) C2F6 (contains a C¬C bond), (d) AsO3 3 -, (e) H2SO3 (H is bonded to O), (f) NH2Cl.. Arrange the bonds in each of the following sets in order of increasing polarity: (a) C¬F, O¬F, Be¬F; (b) O¬Cl, S¬Br, C¬P; (c) C¬S, B¬F, N¬O. What is the Lewis symbol for each of the following atoms or ions? (a) K, (b) As, (c) Sn2 + , (d) N3 Write electron configurations for the following ions and determine which have noble-gas configurations: (a) Cd2+, (b) P3-, (c) Zr4+arrow_forwardAn elemental analysis of a hydrocarbon, which contains only carbon and hydrogen, shows the mass%: element mass% carbon 92.26 hydrogen 7.743 (A) * Determine the empirical formula of the hydrocarbon. (B) The compound has a molar mass of 26.04 g/mol. Determine its molecular formula. (C, Draw the Lewis structure of the molecular compound. Count the total number of sigma bonds and pi bonds each, present in the molecule. (D, What is the hybridization of carbon in the molecule? Explain.arrow_forward
- Ortho-Dichlorobenzene, C6H4Cl2, is obtained when two ofthe adjacent hydrogen atoms in benzene are replaced withCl atoms. A skeleton of the molecule is shown here. (a) Completea Lewis structure for the molecule using bonds andelectron pairs as needed. (b) Are there any resonance structuresfor the molecule? If so, sketch them. (c) Are the resonancestructures in (a) and (b) equivalent to one another asthey are in benzene?arrow_forwardAcetylene (C2H2) and nitrogen (N2) both contain a triplebond, but they differ greatly in their chemical properties.(a) Write the Lewis structures for the two substances. (b) By referring to Appendix C, look up the enthalpies of formationof acetylene and nitrogen. Which compound is more stable?(c) Write balanced chemical equations for the completeoxidation of N2 to form N2O5(g) and of acetylene to formCO2(g) and H2O(g). (d) Calculate the enthalpy of oxidationper mole for N2 and for C2H2 (the enthalpy of formationof N2O5(g) is 11.30 kJ/mol). (e) Both N2 and C2H2 possesstriple bonds with quite high bond enthalpies (Table 8.3).Calculate the enthalpy of hydrogenation per mole for bothcompounds: acetylene plus H2 to make methane, CH4;nitrogen plus H2 to make ammonia, NH3.arrow_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_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
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