B. Determine the substrate and the nucleophile in each pair of reactants. Show the mechanism of the reaction through curved arrows and draw the final product. (B2) CI + + -OH н-о-н
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- For each reaction, draw the complete mechanism and the major organic product(s), paying attention to stereochemistry. (a) (b) OH LOH (еxcess) ? ? CH,Cl2 CH2CI2C) 30. In the presence of a nucleophile, which of the following will undergo conjugate addition? OCH3 HEVL OCH3If anhydrides react like acid chlorides with the nucleophiles, draw the products formed when each of the following nucleophiles reacts with benzoic anhydride [(C6H5CO)2O]: (a) CH3MgBr (2 equiv), then H2O; (b) LiAlH4, then H2O; (c) LiAlH[OC(CH3)3]3, then H2O.
- For each alkyl halide and nucleophile: [1] Draw the product of nucleophilic substitution; [2] determine the likely mechanism (Sn1 or Sn2) for each reaction.2. Draw a reaction mechanism to explain the following reaction. O OH i. OH (aq) LOHH3C-C O: H ethanal :CN: and the electrophile is cyanide ion In the step you have just written, the nucleophile is slow rate-determining Ö—0—1 H3C-C-C=N; adduct
- The given reaction scheme is an example of which type of reaction? O || R₁-C-OH + R₂-OH Oxidation Fischer esterification Nucleophilic substitution Reduction Rearrangement reaction Acid O || R₁-C-O-R₂ Meeting in "General"For the attached alkyl halide and nucleophile: [1] Draw the product of nucleophilic substitution [2] determine the likely mechanism (SN1 or SN2) for each reaction.For the attached alkyl halide and nucleophile: [1] Draw the product of nucleophilic substitution[2] determine the likely mechanism (SN1 or SN2) for each reaction.
- The answer choices for part b ["How would you convert the alkene to a epoxide?"] are: (a) Br2/NaNH2 in liq NH3; (b) mCPBA; (c) OsO4Thank you!2) Rank the following compounds in order of their reaction rates in an SN1 reaction with NaF with 1 being the fastest reaction and 5 being the slowest. OTs Br CI5a) Draw the product(s) of the reaction shown below. Additionally, identify the nucleophile, electrophile and leaving group.