At high temperatures, sulfur vapor is predominantly in the form of
(a) Assuming that the molecular orbitals for third-row diatomic molecules are analogous to those for second-row molecules,construct an MO diagram for the valence orbitals of
(b) Is
(c) What is the bond order of
(d) When two electrons are added to
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LCPO CHEMISTRY W/MODIFIED MASTERING
- Describe the hybridization around the central atom and the bonding in SCl2 and OCS.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_forwardThe cations O2+ and N2+ are formed when molecules of O2 and N2 are subjected to intense, high-energy solar radiation in Earths upper atmosphere. Write the electron configuration for O2+. Predict its bond order and magnetic behavior.arrow_forward
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- Acetylene (C2H2) has a tendency to lose two protons (H+) and form the carbide ion (C22−), which is present in a number of ionic compounds, such as CaC2 and MgC2. (a) What is the bond order of the carbide dianion C22−? (b) For comparison, what is the bond order of C2?arrow_forwardButadiene, C4H6, is a planar molecule that has the followingcarbon–carbon bond lengths: (a) Predict the bond angles around each of the carbon atoms and sketch the molecule. (b) From left to right, what is the hybridization of each carbon atom in butadiene? (c) The middle C—C bond length in butadiene (1.48 Å) is a little shorter than the average C—C single bond length (1.54 Å). Does this imply that the middle C—C bond in butadiene is weaker or stronger than the average C—C single bond? (d) Based on your answer for part (c), discuss what additional aspects of bonding in butadiene might support the shorter middle C—C bond.arrow_forward(a) Write a single Lewis structure for SO3 , and determine the hybridization at the S atom. (b) Are there other equivalent Lewis structures for the molecule? (c) Would you expect SO3 to exhibit delocalized π bonding?arrow_forward
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