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1-The bond order of a diatomic molecule is defined A. as one half the difference between the number of electrons in bonding orbitals, nb, and the number of electrons in antibonding orbitals, na. 2- In heteronuclear diatomic molecules, such as CO we must have additional molecular orbitals. 3- We have writing electronic configuration of [FeCl] complex as 4- The energy gap is referred to asA (10 Da) B. -4 Ao C. E(2g) - 43o while E(eg) = +630 D. point their lobes directly at the point- charge ligands E. -640 F. Four long bond, two short compressed G. Crystal Field Stabilization Energy H. The overlap of "p" orbitals results in two sets of s orbitals (two bonding and two antibonding) and one set of p orbitals (one bonding and one antibonding). L point their lobes between the point charges. J. referred to the crystal field splitting 5- CFSE 6- dz and d- 7- dey, dxz, dyz S- CFSE of d' in high spin 9-Z-in distortion 10-CPSE of d in high spin energy K. (al)2(12)6(e)2(t2")3

1-The bond order of a diatomic molecule is defined A. as one half the difference between the number of electrons in bonding orbitals, nb, and the number of electrons in antibonding orbitals, na. 2- In heteronuclear diatomic molecules, such as CO we must have additional molecular orbitals. 3- We have writing electronic configuration of [FeCl] complex as 4- The energy gap is referred to asA (10 Da) B. -4 Ao C. E(2g) - 43o while E(eg) = +630 D. point their lobes directly at the point- charge ligands E. -640 F. Four long bond, two short compressed G. Crystal Field Stabilization Energy H. The overlap of "p" orbitals results in two sets of s orbitals (two bonding and two antibonding) and one set of p orbitals (one bonding and one antibonding). L point their lobes between the point charges. J. referred to the crystal field splitting 5- CFSE 6- dz and d- 7- dey, dxz, dyz S- CFSE of d' in high spin 9-Z-in distortion 10-CPSE of d in high spin energy K. (al)2(12)6(e)2(t2")3

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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1-The bond order of a diatomic molecule is defined A. as one half the difference between the number of electrons in bonding orbitals, nb, and the number of electrons in antibonding orbitals, na. 2- In heteronuclear diatomic molecules, such as CO we must have additional molecular orbitals. 3 We have writing electronic configuration of (FeCla]" complex as В. -4 Ao C. E(12g) = 4Ao while E(eg) = +6Ao D. point their lobes directly at the point- charge ligands 4- The energy gap is referred to as A (10 Da) 5- CISE 6- dz and ds- y E. -6Ao F. Four long bond, two short compressed G. Crystal Field Stabilization Energy H. The overlap of "p" orbitals results in two sets of s orbitals (two bonding and two antibonding) and one set of p orbitals (one bonding and one antibonding). I. point their lobes between the point 7- dxy, dxz, dyz 8- CFSE of d' in high spin 9-Z-in distortion charges. J. referred to the crystal field splitting 10- CFSE of de in high spin energy K. (al)2(12)6(e)2(12")3 D C A 1 2 4 6 7 8 9. LO B.
Transcribed Image Text:1-The bond order of a diatomic molecule is defined A. as one half the difference between the number of electrons in bonding orbitals, nb, and the number of electrons in antibonding orbitals, na. 2- In heteronuclear diatomic molecules, such as CO we must have additional molecular orbitals. 3 We have writing electronic configuration of (FeCla]" complex as В. -4 Ao C. E(12g) = 4Ao while E(eg) = +6Ao D. point their lobes directly at the point- charge ligands 4- The energy gap is referred to as A (10 Da) 5- CISE 6- dz and ds- y E. -6Ao F. Four long bond, two short compressed G. Crystal Field Stabilization Energy H. The overlap of "p" orbitals results in two sets of s orbitals (two bonding and two antibonding) and one set of p orbitals (one bonding and one antibonding). I. point their lobes between the point 7- dxy, dxz, dyz 8- CFSE of d' in high spin 9-Z-in distortion charges. J. referred to the crystal field splitting 10- CFSE of de in high spin energy K. (al)2(12)6(e)2(12")3 D C A 1 2 4 6 7 8 9. LO B.
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