Draw a reasonable step-wise mechanism for the following transformation being careful to indicate which step is likely rate-determining by writing "rds" above the arrow for that step. S.e NaOCH2CH3 CH3CH2OH
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- Draw a stepwise mechanism for the attached reaction that illustrateshow two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a weak nucleophile (CH3OH) under SN1 reactionconditions, even though it is a 1 ° alkyl halide.Draw a stepwise, detailed mechanism for the following reaction. CH3NH2 N-CH3 CH,NH, Cr (excess)Draw the reactant(s) required for the following transformation. Include any relevant stereochemistry.
- Draw the product of this reaction and states its IUPAC name, and states what type of mechanism is occuring (eg. SN1, SN2, E1, E2, etc)?Draw a step-wise mechanism for the following substitution reaction. Be sure to add lone pairs and charges where relevant. CI H₂OAnswer the question below the reaction. ta The reaction above proceeds through which type of mechanism? SN2 SN1 E1 E2 OH + Excess NH4C1 H₂SO4 + H₂O
- Draw a detailed mechanism for the FeBr3@catalyzed reaction of ethylbenzene with bromine, and show why the sigma complex (and the transition state leading to it) is lower in energy for substitution at the ortho and para positions than it is for substitution at the meta position.5) Only one product is observed in this reaction. Draw the product and briefly explain why. Hint: It is NOT due to the Zaitsev rule. H3PO4 OH H₂O3. Draw a stepwise detailed mechanism for the following reaction showing all the substitution and the elimination products formed. Label the type of the mechanism (SN1, SN2, E1 or E2). Show stereochemistry when applicable. Br "D CH₂CH₂OH H₂O thor through
- The reaction of 3-methylhex-3-ene with HBr produces two stereoisomers. Draw the two-step mechanism, using good curved arrow notation. Identify the HOMO and LUMO in both steps and explain why two products are formed, along with the optical activity of the solution.Complete the following stepwise reaction mechanism problems based on the reaction conditions given: Draw the stepwise mechanism.Rank the set of compounds in order of reactivity (fastest to slowest) in a nucleophilic addition-elimination reaction with a nucleophile such as CH3NH2.