Concept explainers
Carbon monoxide (CO) forms bonds to a variety of metals and metal ions. liS ability to bond to iron in hemoglobin is the reason that CO is so toxic. The bond carbon monoxide forms to metals is through the carbon atom:
a. On the basis of electronegativities, would you expect the carbon atom or the oxgen atom to form bonds to metals?
b. Assign formal charges to the atoms in CO. Which atom would you expect to bond to a metal on this basis?
c. In the MO model, bonding MOs place more electron density near the more electronegative atom. (See the HF molecule in Figs. 4-54 and 4-55.) Antibonding MOs place more electron density near the less electronegative atom in the diatomic molecule. Use the MO model to predict which atom of carbon monoxide should form bonds to metals.
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Chapter 9 Solutions
Chemistry
- 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_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_forwardIt is possible to write a simple Lewis structure for the SO42- ion, involving only single bonds, which follows the octet rule. However, Linus Pauling and others have suggested an alternative structure, involving double bonds, in which the sulfur atom is surrounded by six electron pairs. (a) Draw the two Lewis structures. (b) What geometries are predicted for the two structures? (c) What is the hybridization of sulfur in each case? (d) What are the formal charges of the atoms in the two structures?arrow_forward
- Consider 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_forwardThe chemistry of the nitrite ion and HNO2: (a) Two resonance structures are possible for NO2. Draw these structures, and then find the formal charge on each atom in each resonance structure. (b) In forming the acid HNO2 an H+ ion attaches to the O atom and not the N atom of NO2. Explain why you would predict this result. (c) Two resonance structures are possible for HNO2. Draw these structures, and then find the formal charge on each atom in each resonance structure. Is either of these structures strongly preferred over the other?arrow_forwardThe 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_forward
- An important observation supporting the concept of resonance in the localized electron model was that there are only three different structures of dichlorobenzene (C6H4C10). How does this fact support the concept of resonance (see Exercise 89)?arrow_forwardGive 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_forwardComplete the following resonance structures for POCl3. a. Would you predict the same molecular structure from each resonance structure? b. What is the hybridization of P in each structure? c. What orbitals can the P atom use to form the bond in structure B? d. Which resonance structure would be favored on the basis of formal charges?arrow_forward
- Define formal charge and explain how to calculate it. What is the purpose of the formal charge? Organic compounds are composed mostly of carbon and hydrogen but also may have oxygen, nitrogen, and/or halogens in the formula. Formal charge arguments work very well for organic compounds when drawing the best Lewis structure. How do C, H, N, O, and Cl satisfy the octet rule in organic compounds so as to have a formula charge of zero?arrow_forward(a) Draw a Lewis structure for the ozone molecule, O3. (The order of atom attachment is OOO, and they do not form a ring.) Chemists use ozone to cleave carbon-carbon double bonds (Section 6.5C). (b) Draw four contributing resonance structures; include formal charges. (c) How does the resonance model account for the fact that the length of each OO bond in ozone (128 pm) is shorter than the OO single bond in hydrogen peroxide (HOOH, 147 pm) but longer than the OO double bond in the oxygen molecule (123 pm)?arrow_forwardSeveral 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_forward
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