Concept explainers
The heavier halogens (CI, Br, and I) form compounds in which the central halogen atom, X, is bonded directly to oxygen and to fluorine. Several examples are known, including those with formulas of the type
a. chloryl fluoride,
b. perchloryl fluoride,
c.
Trending nowThis is a popular solution!
Chapter 22 Solutions
GENERAL CHEMISTRY(LL)-W/MASTERINGCHEM.
- Best Lewis Formula and Molecular Geometry A student writes the Lewis electron-dot formula for the carbonate anion, CO32, as a Does this Lewis formula obey the octet rule? Explain. What are the formal charges on the atoms? Try describing the bonding for this formula in valence bond terms. Do you have any difficulty doing this? b Does this Lewis formula give a reasonable description of the electron structure, or is there a better one? If there is a better Lewis formula, write it down and explain why it is better. c The same student writes the following resonance description for CO2: Is there something wrong with this description? (What would you predict as the geometries of these formulas?) d Is one or the other formula a better description? Could a value for the dipole moment help you decide? e Can you write a Lewis formula that gives an even better description of CO2? Explain your answer.arrow_forwardPredict die molecular structure and bond angles for each molecule or ion in Exercises 88 and 94. a. POCl3, SO42, XeO4, PO43, ClO4 b. NF3, SO32, PO33, ClO3 c.ClO2, SCl2, PCl2 d. Considering your answers to parts a, b, and c. what conclusions can you draw concerning the structures of species containing the same number of atoms and the same number of valence electrons? (O3), sulfur dioxide, and sulfur trioxide.arrow_forwardA variety of chlorine oxide fluorides and related cations and anions are known. They tend to be powerful oxidizing and fluorinating agents. FClO3 is the most stable of this group of compounds and has been studied as an oxidizing component in rocket propellants. Draw a Lewis structure for F3ClO, F2ClO2+, and F3ClO2. What is the molecular structure for each species, and what is the expected hybridization of the central chlorine atom in each compound or ion?arrow_forward
- Give two requirements that should be satisfied for a molecule to be polar. Explain why CF4 and XeF4 are nonpolar compounds (have no net dipole moments) while SF4 is polar (has a net dipole moment). Is CO2 polar? What about COS? Explain.arrow_forwardFor many years after they were discovered, it was believed that the noble gases could not form compounds. Now we know that belief to be incorrect. A mixture of xenon and fluorine gases, confined in a quartz bulb and placed on a windowsill, is found to slowly produce a white solid. Analysis of the compound indicates that it contains 77.55% Xe and 22.45% F by mass. (a) What is the formula of the compound? (b) Write a Lewis structure for the compound. (c) Predict the shape of the molecules of the compound. (d) What hybridization is consistent with the shape you predicted?arrow_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_forward
- Several Lewis structures can be written for perbromate ion, , the central Br with all single Br—O bonds, or with one, two, or three Br=O double bonds. Draw the Lewis structures of these possible resonance structures, and use formal charges to predict which makes the greatest contribution to the resonance hybrid.arrow_forwardLight of appropriate wavelength can break chemical bonds. Light having λ < 240 nm can dissociate gaseous O2. It requires light with λ < 819 nm to dissociate gaseous H2O2 to 2 OH. Assume that all of the photon energy is used solely for these dissociations. (a) Calculate the energy required to dissociate (i) O2 and (ii) H2O2. (b) Consider the results of part (a). How well do they correlate with the Lewis structures of O2 and H2O2? Explain your answer.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
- The molecule shown here. 2-furylmelhanethiol, is responsible for the aroma of coffee: (a) What are the formal charges on the S and O atoms? (b) Give approximate values of angles 1, 2, and 3. (c) Which are the shorter carbon-carbon bonds in the molecule? (d) Which bond in this molecule is the most polar? (e) Is the molecule polar or nonpolar? (f) The four C atoms of the ring are all in a plane. Is the O atom in that same plane (making the five-member ring planar), or is the O atom bent above or below the plane?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_forwardCould the anion Li2 exist? What is the ions bond order?arrow_forward
- 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 Learning
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning