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- A mechanism pattern involved in this reaction is loss of a leaving group rearrangement nucleophilic attack substitutiondraw the mechanismFor the reaction shown below, circle the major product obtained when the | reaction is allowed to reach equilibrium. Place a box around the product that is formed the fastest. а H2C= CI H-CI CIH2C CIH,C H3C CI CI `CH3 H2C CIH,C H;C CI
- 6. Predict the reactant (starting material) for the reaction and propose a mechanism. NaCN SN2 NaOH E2 CN a Ph PhComplete the following reversible reaction and draw the mechanism of formation ofproducts. Indicate using the arrows of unequal length whether the shift in equilibrium will favor the reactants or the products. give 2 reasonsI need the reaction mechanism of this step
- Which of the following is considered an initiation reaction: O CH₂ CH₂ H-H -CH₂ -CH₂ H₂C-CH₂ H-CH₂ H₂C-CH₂ H. -CH3 H₂C-H H-CH₂ -CH₂ -CH₂The Reaction intermediate in the reaction C2H6 Cl2 C2H5CI HCI O Carbanion O Free radical O Carbocation Transition state Next pageDraw the complete reaction mechanism for the following reactions. Hint: Problem #4 will have a rearrangement. 1) но HBr OH 2) HBr 3) OH H,SO, OH 4) H,SO.