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Are the ligand labels La (Scheme 1) ad L1 (Table 2) consistent? How did you arri

ID: 716443 • Letter: A

Question

Are the ligand labels La (Scheme 1) ad L1 (Table 2) consistent? How did you arrive at your answer? (Note: Lb is L2 and Lc is L3) Table 2: Calculated geometric parameters of SiO2 A and complexes B-E, Gibbs free energies ( G [kcal mol 1) for the formation of complexes (B-E), and electronic charges (Q(SiO2)) of the Sio2 fragment in complexes B-E. Ph Ph 1.877 1.900 1.971 1.5501 1.555 o-si-o Ar-N P :Si N1.507 1.507 1527 1.527 1.527 1.589 o-si-o (60 °C) 1.544 T1.829 o-si-o 1744.1 784 Ph 1725 185, 2007 NHC-1 D-A D-A D-A Ar-N PR O-Si-o L-Si-D(L) 129.0 109.0 151.8 139.2 99.2 180 2 Ph Ph a DMAP b Pyridine L1 0.0 L2 0.0 L3 0.0 -45.9 -39.4 55.4 -65.9 -65.9 65.9 -86.5 -81.8 -83.0 -69.3 -65.5 -74.9 AG LRT 0-Sio Q(sio2) L L2 0.068-0.1640.474 0.213-0.068 -0.1620.465 0.348 -0.068 -0.306 -0.583 R- Pr(NHC-1) Me (NHC-2) Key: LI-DMAP, L2= Py, L3-NHGI, D/A-donor-acceptor imino- phosphorane ligand (R-CPh CHPh, Ar-2,6-iPr2CsH) Scheme 1. Synthesis of Si,0, complex 2 and Sio2 complex 3

Explanation / Answer

Yes the ligands are capable of doing this because u can't get any Lewis acid without extraxtex

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