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- According to this video, https://www.youtube.com/watch?v=9Ng6Zv9oLzk, draw the dienophile that was used in the example explaining s-cis and explain what is different about this dienophile from common examples?Fill in the blank completely including stereochemistry if necessary.In testosterone molecule, assign R or S configuration in Carbon 3. Explain/show how. Is Sn2 Reaction possible for 1-bromo-2,2-dimethylpropane? Yes or no Pls Explain :)
- up an example (not appearing in this ChemActivity) of a pair of molecules that are a)constitutional isomers, b) conformers. c) configurational stereoisomers.How many stereoisomers of 2-methyl-heptan-4-ol could form? How many would you expect to form? In what ratios? (All equal?). Explain your answer Please explain clearly why the ratio is 1:1. Thank you!Draw the most stable carbocation that can be formed by the compound in Figure 5. [Generate a SMILES notation: https://jsme-editor.github.io/dist/JSME_test.html. Copy the notation (CTRL+C) and paste it as the answer to this question (CTRL+V).] *
- Benzene is one of the compounds used as octane enhancers in unleaded gasoline. It is manufactured by the catalytic conversion of acetylene to benzene: 3C2 H2(g) ⟶ C6 H6(g). Which value of Kc would make thisreaction most useful commercially? Kc ≈ 0.01, Kc ≈ 1, or Kc ≈ 10. Explain your answer.Draw the organic product(s) of the following reaction. You do not have to consider stereochemistry. Include cationic counter-ions, e.g., Na+ in your answer, but draw them in their own sketcher. If no reaction occurs, draw the organic starting material. Separate multiple products using the + sign from the drop-down menu.Can someone please explain the logic of 2 vs 3 for stereochemistry? They are both C-C so I don't understand how to rank 2 vs 3. Thank you!