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- Room Date: Name Lab Day/Time Partner Name: Instructor Set 1 Questions: Investigating Number of Bonds 1 Based ofT your observations above compare the Lewis structures and the bond lengtn What conclusion can you make about the relationship between the number of bonds and bond length? 2. Why would the amount of bonds change the bond length? (May have to refer to book or lecture notes) 3. Did the change in the number of bonds and the bond lengths affect the type of molecular geometry? Why or Why not?See the Attachment & Answer the following question? Ques: In what type of orbital does the lone pair on each N atom reside?Which of the highlighted chemical bonds in the molecules below is longest? Shortest? In between? Which highlighted bond requires the highest energy to break? Lowest? In between? Answer these questions by completing the second and third columns in the table. length of highlighted bond energy of highlighted bond compound :0: choose one- choose one H-C-H :CE0: -choose one - choose one H-C-0-H choose one - choose one H. Submit A HIC
- Part B Below are the molecular orbitals of benzene. Rank them in order of increasing energy based on the number of nodes. Consider that the blue color indicates one phase and the red color indicates the other phase of the orbital. Rank from lowest energy to highest energy. To rank items as equivalent, overlap them. ► View Available Hint(s) Lowest energy The correct ranking cannot be determined. Submit H B Reset Help Highest energyFigure 3 of 3 Which of the following clusters of orbitals would form the shape shown here (Figure 3) either through the formation of a single molecule or by bonding to another atom of similar electronic geometry and results in an arrangement of orbitals that is possible within the valence shell of an atom? Check all that apply. ► View Available Hint(s) two sp orbitals and two p orbitals six sp³ d² orbitals three sp orbitals two sp orbitals and four p orbitals three p orbitals six sp³ d orbitals six sp³ orbitals one sp orbital and two p orbitalsNew Tab The resonance hybrid representation of O3 more stable than either one of the individual resonance structure representations - concisely explain this. (multiple answers) Multiple answers: Multiple answers are accepted for this question Select one or more answers and submit. For keyboard navigation... SHOW MORE V Electrons that participate in resonance have lower potential energy due to reduction of e-- e- a repulsions with atomic electrons Electrons that participate in resonance have higher potential energy due to reduction of e-- e- repulsions with atomic electrons Electrons that participate in resonance have lower kinetic energy due to an increase in the bonding orbit Electrons that participate in resonance have higher kinetic energy due to an increase in the d bonding orbit
- O CHEMICAL BONDING OD OO Heather Recognizing typical LCAO molecular orbitals The dark dots in this sketch are the nuclei. Now use the sketch to complete the table below. Write the symbol for this MO. O* O bonding Is this a bonding or antibonding MO? O antibonding O higher O lower What is the energy of this MO, compared to the energy of a 3p orbital on one of the separate atoms? O the same not enough information to decide Explanation Check © 2021 McGraw-Hill Education. All Rights Reserved. Terms of Use I Privacy | Accessibility IIWhich of these bonds is weakest? *See ImageNumber of Molecule valence electrons Formal Charge Electron-Group Geometry Molecular Geometry Resonance AIH2ATCI- Al: Al: Select one.. Al: Select one .. Select one ... AIHAT,Br Al: Al: Select one ... Al: Select one ... Select one ... FSIAS Si: Si: Select one .. Si: Select one ... Select one .. PHATCI P: P: Select one ... P: Select one.. Select one .. PCIFI P: P: Select one ... P: Select one ... Select one ... v
- Group the following molecular formulas under their respective geometries. Use the Real Molecules mode to verify the correct geometry for select structures. Drag the appropriate items to their respective bins. > View Available Hint(s) Reset Help BeCl2 SF. CO2 CH4 PCl, HCN BF3 PF, CH20 NH4+ Linear Trigonal planar Tetrahedral Trigonal bipyramidal OctahedralPLEASE hightlight the bonds that need to be highlighted and in which color!HCN is a molecule with ["1", "2", "3", "4"] electron domains giving it a ["trigonal planar", "linear", "tetrahedral"] electron domain geometry. It has ["3", "4", "2", "1"] bonded atoms and ["0", "3", "1", "2"] lone pairs. HCN will exhibit a ["bent", "linear", "trigonal planar", "tetrahedral", "trigonal pyramidal"] molecular geometry.