What is the major organic product of this reaction? (i) CH3CH2MgBr (ii) H+ Give detailed mechanism Solution with explanation needed of each steps. don't give Handwritten answer
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- Provide the major organic product of the reaction below explain the mechanismPredict the organic product(s) of the following reactions. Clearly indicate which product is major if applicable. a) b) Br NaOMe MeOH HeatWhich of the following series of reactions is a viable route form the starting material to the product shown below? The correct route is option B but please inlcude a detailed description explaining why and a step by step process:)
- For each of the reactions shown below, draw the structure of the major organic product(s) or starting material. Give only one structure per box and indicate stereochemistry where applicable. CH3 NaSH (a) H- -Br H- -OCH3 acetone CH2CH3 (b) (c) fo (d) 3 Br Br₂/light NaOtBu tBuOH OH H₂O monobrominated product monobrominated product(d) Propose a reaction mechanism to account for the following reaction. AIC3Give the mechanistic Symbols CE1, E₂, SN, SN²) that are Con Sistent with Statemenst! most each of the following O Methyl halides react with Sodium ethoxide in eth and only by this mechanism In ethanol that contains Sodiumn ethoxide, tert-butyl bromide reacts mainly by this mechanism c) these reaction Con certed DJ these involve are mechanisms infere processes reactions mechanisms carbc cation intermedites E) Reactions proceeding by mechanisms are these Sterospecific
- 1. Propose a plausible mechanism for the reaction schemes below using curved arrow notation to illustrate electron flow; be sure to show all charges and intermediates. () mechanism a) OH 1 eq. Cl₂ 2 + HCI mechanism b) D2SO4 озвProvide the mechanism for the following reaction (1) PhMgBr (2 equiv) (2) H3O+ workup OHGive the detailed mechanism for the following nitration reaction. Show the contributing resonance structures and the resonance hybrid for the intermediates. HNO,, H,SO, NO2
- Predict the major products of the following reactions.(a) cis@hex@2@ene + mCPBA in chloroform(b) trans@hex@3@ene + peroxyacetic acid (CH3CO3H) in water(c) 1@methylcyclohexene + MMPP in ethanol(d) trans@cyclodecene + peroxyacetic acid in acidic water(e) cis@cyclodecene + mCPBA in CH2Cl2, then dilute aqueous acidWhich of the following best describes a key step in the mechanism for the reaction below? HO, ... -CH3 -CH3 + en dihydroxylation H3C- H3C- OH (A) free-radical substitution at the carbonyl carbon B elimination reaction by abstraction of a beta-hydrogen nucleophilic attack by an alkene to form a cyclic (epoxide) intermediate electrophilic addition reaction to form a carbocation intermediateGive the expected major product for each reaction, including stereochemistry where applicable.(a) but@1@ene + H2>Pt (b) cis@but@2@ene + H2>Ni