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- Show the steps of the next reaction in detail. And explain why it's hard to go along with the dotted line.the following reaction mechanism contains mistakes. which of the following statements correctly describes the curved arrows consistent with the reaction?The rate of bromination of the following three alkenes: 2-methyl-1-pentene, 2-methyl-2-pentene, 3-methyl-1-pentene. Please rank them in order from slowest to fastest to react. Thank you
- 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 + CI5. For the following pairs of species, which is the strongest nucleophile in acetone? Explain. By ü) yplease help complete the appropriate mechanism arrows for each transformation (in a saponification reaction) and What small molecule is being generated by this reaction in the third step of the mechanism
- The following compounds are major products of an elimination reaction with an alkyl halide. Determine the structure of the alkyl halide. (P.S. write the overall reaction mechanism). Tip: Remember your Markovnikov’s rule. Follow the progress of the reaction and look at the stability of the intermediate products and transition states to determine the minor and major products. ANSWER ONLY THE FIRST 3 LETTERS.Rank the following substrates in order from slowest E1 reaction rate to fastest. Br Br Br Br A Bcan someone complete the following mechanism with all steps?
- Place these compounds in order from fastest to slowest in an SN2 reaction (list the letters of the compounds from fastest to slowest). There are 5 compounds.The reaction below requires several mechanistic steps. Six different intermediates are shown below...some are involved in the mechanism and some are not. Your job is to pick the correct intermediates and put them in the correct order. Your answer should be formatted using the number of the first intermediate, followed by the number of the second intermediate, followed by the number of the third intermediate, etc., until you have selected the correct intermediates and placed them in the correct order for the mechanism. An example of the correct answer format would be 231 if you thought intermediate #2 should come first, followed by intermediate #3, and then lastly, intermediate #1. Again, not all of the intermediates are included in this mechanism, so it might be a good idea to try to work it out first on your scratch paper. Do not add any spaces in your answer. HCI đ HO CH₂Cl₂ (solvent) Н. H10O Н HO Intermediate 1 Intermediate 4 + HO H Intermediate 2 Intermediate 5 **** O: HO :0…In an E2 mediated elimination reaction of an alkyl halide (H-X) using NaOCH3 as base, which of the following statement is not true? O The reactivity order for alkyl halides (RX) is tertiary secondary> primary. O The rate of reaction = k2 (alkyl halide] [NaOCH₂] O The reaction occurs in a single step. O The rate is independent of the leaving group.