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- Draw the structure of the organic product that is formed when the compound shown below is treated with the following reagents: 1) TsCl, pyridine; 2) NaCN. Interactive 3D display mode H₂Cl OH Draw the molecule on the canyas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single beWhich of the following best describes compound 3? It is an… alcohol anhydride thiol amine nitrileim very confused someone help me please
- Profiles Tab Window Help ALEKS - Tiffany Te-L-Peng - L X = sl.exe/10_u-IgNslkr7j8P3jH-liGBdp5ulp5VqUnMDyPOVaX6q0CRPLZSQ5NeEtFRBekLt6yRz O SUBSTITUTION REACTIONS Identifying resonance stabilized carbocation intermediates in... Substrate For each of the substrates below, identify whether: (A) the rate of substitution doesn't depend on nucleophile concentration and (B) the product distribution from substitution gives a 50/50 mix of enantiomers. If you answered "yes" for the first susbtrate, draw the intermediate that forms during a nucleophilic substitution reaction in the space below the table. 'Br á Br Are both A and true? Oyes Ono + Oyes O no Oyes Ono Oyes Ono ㅂ Click and drag to start drawing a structure. X C с X Tiffakeferences Draw the structure(s) of the major organic product(s) of the following reaction. H. PPH3 THE • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If the reaction produces a racemic mixture, draw both stereoisomers. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Include anionic counter-ions, e.g., I-, in your answer, but draw them in their own sketcher. C opy asteDraw curved arrows indicating the movement of electrons in. The third step of the mechanism