(a)
Interpretation:
The hybrid orbitals has to be described in the given molecules or ions.
Concept Introduction:
Hybrid orbitals:
Hybrid orbitals are formed from the combination of atomic orbitals of the isolated atom. Hybrid orbitals are used to describe the formation of bonds in the directions predicted by VSEPR model.
(b)
Interpretation:
The hybrid orbitals has to be described in the given molecules or ions.
Concept Introduction:
Valence bond theory: VSEPR theory tells about the shapes of molecules and ions by taking the consideration that the outermost electron pairs are arranged about each atom so that the pairs of electrons are kept at a distance from one molecule to other, thereby minimizing the repulsion of electron-pair.
Hybrid orbitals:
Hybrid orbitals are formed from the combination of atomic orbitals of the isolated atom. Hybrid orbitals are used to describe the formation of bonds in the directions predicted by VSEPR model.
Want to see the full answer?
Check out a sample textbook solutionChapter 10 Solutions
General Chemistry - Standalone book (MindTap Course List)
- In the molecular orbital mode l, compare and contrast bonds with bonds. What orbitals form the bonds and what orbitals form the bonds? Assume the z-axis is the internuclear axis.arrow_forwardMolecular Orbital Theory (See Examples 9.49.6.) The hydrogen molecular ion, H2+, can be detected spectroscopically. Write the electron configuration of the ion in molecular orbital terms. What is the bond order of the ion? Is the hydrogenhydrogen bond stronger or weaker in H2+ than in H2s?arrow_forwardCalcium cyanamide, CaNCN, is used both to kill weeds and as a fertilizer. Give the Lewis structure of the NCN2 ion and the bonded-atom lone-pair arrangement and hybridization of the carbon atom.arrow_forward
- Consider the polyatomic ion IO65-. How many pairs of electrons are around the central iodine atom? What is its hybridization? Describe the geometry of the ion.arrow_forwardIn propene CH3CH=CH2, the first carbon has sp3 hybrid orbitals and the second carbon has sp2 hybrid orbitals. These orbitals interact to make a bond. Why are these hybrid orbitals not orthogonal?arrow_forwardMethylcyanoacrylate is the active ingredient in super glues. Its Lewis structure is (a) How many sigma bonds are in the molecule? (b) How many pi bonds are in the molecule? (c) What is the hybridization of the carbon atom bonded to nitrogen? (d) What is the hybridization of the carbon atom bonded to oxygen? (e) What is the hybridization of the double-bonded oxygen?arrow_forward
- Why is the concept of hybridization required in valence bond theory?arrow_forwardSpecify the electron-pair and molecular geometry for each underlined atom in the following list. Describe the hybrid orbital set used by this atom in each molecule or ion. (a) BBr3 (b) CO2 (c) CH2Cl2 (d) CO32arrow_forwardAspirin, or acetylsalicylic acid, has the formula C9H8O4 and the skeleton structure (a) Complete the Lewis structure and give the number of bonds and bonds in aspirin. (b) What is the hybridization about the CO2H carbon atom (colored blue)? (c) What is the hybridization about the carbon atom in the benzene-like ring that is bonded to an oxygen atom (colored red)? Also, what is the hybridization of the oxygen atom bonded to this carbon atom?arrow_forward
- What hybrid orbitals would be expected for the central atom in each of the following molecules or ions?arrow_forwardDo lone pairs about a central atom affect the hybridization of the central atom? If so, how?arrow_forwardPiperine, the active ingredient in black pepper, has this Lewis structure. (a) Give the values for the indicated bond angles. (b) What is the hybridization of the nitrogen? (c) What is the hybridization of the oxygens?arrow_forward
- General Chemistry - Standalone book (MindTap Cour...ChemistryISBN:9781305580343Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; DarrellPublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningPhysical ChemistryChemistryISBN:9781133958437Author:Ball, David W. (david Warren), BAER, TomasPublisher:Wadsworth Cengage Learning,
- Chemistry by OpenStax (2015-05-04)ChemistryISBN:9781938168390Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark BlaserPublisher:OpenStaxChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning