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- Give 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 SterospecificPredict the product(s) and provide the complete mechanism for each reaction below.3. Provide the mechanism for the following reactions showing the major product only, include generation of electrophile if appropriate. You don't need to show the resonance contributors of the intermediate- H,C ČH, AICI,
- Consider the reaction scheme shown below. HCI [1] ОН (a) Provide a detailed mechanism for reaction [1].Predict the major most products of the following reactions or reaction sequences. Mechanisms are not required for your answers to these questions. In sequences, partial credit can be earned by correctly identifying products of each step in the sequence. 1) NaH, THF H-= 2) 3) H₂0Ⓒ 0-H- 1) PhMgBr, ether 2) H₂O Ⓒ b) d) HO OH OTS [(Pr)₂CuCN)Li₂, THF CHO OH OH MeOH H₂0 cat. A) O3. CH₂Cl₂, -78°C B) (CH3)2SGive the major product of the following reaction. مشن Ph-CEC-H 1) NaNH, 2) CH3CH2CH2CI, ? O There is no reaction under these conditions or the correct product is not listed here.
- Give the detailed mechanism for the following nitration reaction. Show the contributing resonance structures and the resonance hybrid for the intermediates. HNO,, H,SO, NO2Provide the major product of each of the following reactions: What do all these reactions have in common? How do all reactions differ?Br Brz CH3 CH3 H3C CH2CI2 H3C Br Electrophilic addition of bromine, Br2; to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH,Cl). In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product with anti stereochemistry is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions Br: :Br: .CH3 H3C H3C CH3 Br:
- Which of the following molecules will NOT lead to a successful synthesis of a Grignard reagent upon reaction with magnesium? CI https://ibb.co/54Jw34p 2 Me. OMe https://ibb.co/6655LTH Br но https://ibb.co/2nfzPmX O Me `Br https://ibb.co/wo93ymS 2 Br MeO https://ibb.co/Hq2s6ck 21) Complete the following reaction and provide a detailed, step-by-step mechanism for the process. HBr 2) Provide the structure of the major organic product in the reactions below. HI CH3 win H3C. CH3 CH₂CH3 HCI Xero H₂C CH3 HBr(i) OEt OEt 1) NaOEt 2) H3O* workup W 1) NaOEt 2) Br V Compound W can be synthesised in an excellent yield via an intramolecular Claisen reaction of 1,6-diester V. Draw the structure of product W and provide detailed reactions mechanisms to account for its formation. (ii) Draw the product X which would form upon the alkylation reaction of W with the reagents shown.