Draw the step-by-step curved-arrow pushing mechanism of the reaction. Must show where all protons come from and go to. (use of +H*/-H*notations is NOT ALLOWED). All lone pair electrons must be included in your drawing. :O: :O: H₂O :O: он + Но :O:
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- Your answer is incorrect. Predict the relative rates of these reactions. That is, select 1 next to the reaction with the fastest rate, 2 next to the reaction with the next fastest rate, and so on. Note for advanced students: you may assume these reactions all take place in a polar aprotic solvent, like DMSO. Incorrect Your answer is incorrect. Predict the relative rates of these reactions. That is, select I next to the reaction with the fastest rate, 2 next to the reaction with the next fastest rate, and so on. Note for advanced students: you may assume these reactions all take place in a polar aprotic solvent, like DMSO. Reaction Relative Rate G + H₂O - OH₂ 2 Br + H₂S - + Br 3 + H₂S SHI + ci I (fastest) Br + H₂O OM₂ + Br 4 (slowest)Explains the mechanism step by step. Thank you for the help.Predict the relative rates of these reactions. That is, select 1 next to the reaction with the fastest rate, 2 next to the reaction with the next fastest rate, and so on. Note for advanced students: you may assume these reactions all take place in a polar aprotic solvent, like DMSO. ( Choose one) Predict the relative rates of these reactions. That is, select 1 next to the reaction with the fastest rate, 2 next to the reaction with the next fastest rate, and so on. Note for advanced students: you may assume these reactions all take place in a polar aprotic solvent, like DMSO. u + H₂O Reaction - OH₂ Relative Rate (Choose one) OH₂ (Choose one) ▼ +CI ... + H₂O OH + OH + I (Choose one) (Choose one) ▼ + H₂S + CI
- Predict the product of the reaction between phenol (a) (Б) (c) MgBr (d) (C6H5OH) and each of the compounds shown here. Hint: First determine which elementary step is likely to occur. CH;OK CH;Li LIAIH,Please do question 12 and or any other questions. However, please explain the mechanism in detailIt’s directly or indirectly reaction. Answer with details please
- Predict the initial and isolated products for the reaction. Hint: the products are isomers and in equilibrium with each other.Draw the complete, detailed mechanism and predict the products for the following reactions. HCN KCN, H2O (a) HCN NaOH, H20 (b)Which of the following two reactions would you predict to go faster and why?.
- Draw the reaction mechanism without the catalyst C4H7O2NS. You can use either H+ or OH- in the solutionMatch the reaction with the mechanism that it proceeds through. HO, HO. X catalytic H₂SO4 HBr Br₂ light 1. Free Radical Chain Reaction 2. SN1 3. SN2 4. E1 5. E219. Predict the relative rates of these reactions. That is, select 1 next to the reaction with the fastest rate, 2 next to the reaction with the next fastest rate, and so onNote for advanced students: you may assume these reactions all take place in a polar aprotic solvent, like DMSO.