(a) Describe the molecule xenon trioxide, XeO3, using four possible Lewis structures, one each with zero, one, two, or three Xe—O double bonds. (b) Do any of these resonance structures satisfy the octet rule for every atom in the molecule? (c) Do any of the four Lewis structures have multiple resonance structures? If so, how many resonance structures do you find? (d) Which of the Lewis structures in (a) yields the most favorable formal charges for the molecule?

(a) Describe the molecule xenon trioxide, XeO3, using four possible Lewis structures, one each with zero, one, two, or three Xe—O double bonds. (b) Do any of these resonance structures satisfy the octet rule for every atom in the molecule? (c) Do any of the four Lewis structures have multiple resonance structures? If so, how many resonance structures do you find? (d) Which of the Lewis structures in (a) yields the most favorable formal charges for the molecule?

Chemistry: Principles and Practice

3rd Edition

ISBN:9780534420123

Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer

Publisher:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer

Chapter9: Chemical Bonds

Section: Chapter Questions

Problem 9.72QE: Write all resonance structures of chlorobenzene, C6H5Cl, a molecule with the same cyclic structure...

See similar textbooks

Similar questions

Given the bonds C N, C H, C Br, and S O, (a) which atom in each is the more electronegative? (b) which of these bonds is the most polar?
Using the bond dissociation enthalpies in Table 8.8, estimate the enthalpy of combustion of gaseous methane, CH4, to give water vapor and carbon dioxide gas.
In 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?
Consider 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 briefly
Write the Lewis symbol for atoms of each of the following elements:(a) Al, (b) Br, (c) Ar, (d) Sr.
3) The molecule diphosphorus tetraoxide (P,O,) has two central atoms and four different resonance structures that do not violate the octet rule. Draw two of these resonance structures below. 4) The compound acetone is a common solvent. It has a chemical formula of CH,COCH, Acetone has three central atoms. (a) Draw the Lewis Dot structure for acetone. (b) Give the Ideal Bond Angle for all three central atoms. 5) Four covalent molecules are drawn below. :o: H. H-CH H H (1) (2) (3) (4) a) Define each of these molecules as polar or non-polar. (1) (2) (3) b) Describe the type of intermolecular force that each molecule would use: (1) (2) (3) (4)
(1) What is the total number of valence electrons in the Lewis structure of SF2? electrons (2) Draw a Lewis structure for SF2
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?
Cyanogen (CN)2 is known as pseodohalogen because it has some properties like halogens. It is composed of two CN’s joined together.(i) Draw the Lewis structure for all the possible combination for (CN)2.(ii) Calculate the formal charge and determine which one of the structures that you have drawn is most stable.(iii) For the stable structure, determine the geometry around the two central atoms.(iv) For the stable structure, draw the dipole arrows for the bonds.(v) Base on the stable structure, determine the polarity of molecule and state your reason.
In addition to ammonia, nitrogen forms three other hy-drides: hydrazine (N₂H₄), diazene (N₂H₂), and tetrazene (N₄H₄).(a) Use Lewis structures to compare the strength, length, and or-der of nitrogen-nitrogen bonds in hydrazine, diazene, and N₂.(b) Tetrazene (atom sequence H₂NNNNH₂) decomposes above 0°C to hydrazine and nitrogen gas. Draw a Lewis structure fortetrazene, and calculate ΔH°ᵣₓₙ for this decomposition.
Use Lewis electron-dot symbols to represent the formationof (a) BrF₃ from bromine and fluorine atoms; (b) AlF₃ from alu-minum and fluorine atoms.
Some chemists believe that satisfaction of the octet rule should be the top criterion for choosing the dominant Lewis structure of a molecule or ion. Other chemists believe that achieving the best formal charges should be the top criterion. Consider the dihydrogen phosphate ion, HaPO, , in which the H atoms are bonded to O atoms. (a) What is the predicted dominant Lewis structure if satisfying the octet rule is the top eriterion? (b) What is the predicted dominant Lewis structure if achieving the best formal charges is the top criterion?