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- Benzvl chloride can be converted into benzaldehvde by treatment with nitromethane and base. The reaction involves initial conversion of nitromethane into its anion, followed by SN2 reaction of the anion with benzyl chloride and subsequent Ε2 reaction. Write the mechanism in detail, using curved arrows to indicate the electron flow in each step.40) Predict the major product for the reaction shown. xo 40 IV (CH3)3CCH₂CI AICI 3 A) I B) II V C) III ||| D) IV E) VOIV OV What is the predicted product of the elimination reaction shown? IV OH HO conc. H2SO4 heat || V III
- 2. Predict the product and show the mechanism for the following reaction. a) NaOtBu b) O Hnoitibb ispu c) warm to RT d) H3O+, heat oldo19 visaPredict the products and peouide the mechanism for r eoch reachon below + - NaO WHz pyridine :OCH2CH3 ec) + Na OcHs Na OH BrProvide the product and mechanism for the reaction: ОН Cro, H,SO, H,0
- но CH3CO₂Et LDA, -78 °C NaOEt EtOH in addition to the mechanism predict which product is favoredOrganic Chemistry - Mechanism Show the mechanism of transformations below:Show the mechanism of transformations below: b) OMe 1. NaOMe MeOH Meo, Meo OMe 2. H30* TSOH, A B C) CI Meo OMe MeO OMe NaOMe MeO OMe NaOMe (excesso) (excesso)Answer the following questions from the reaction given below: OH OH 1) BH3-THF 2) NAOH/H2O2 OH C a) What is the major product(s) of the reaction (A-D) ? b) What is the mechanism by which the major product is formed ? c) Is the reaction Regioselective ? Explain DI A.
- )A Which of the following is the product of the reaction shown below? || C H,C CI A) B) C) D) + H OH pyridine HO H O H3C H H OH 0 H CH3 ве B) C OB D) DIII. Give a detailed mechanism for the following reaction: OH ОН1. Predict the product of the following reaction and show the mechanism. a) 1.1 equiv LDA -78 C OH (d b) 0 c) H3O+, heat