5. Now draw the proper arrows for these transformations. These are all first semester mechanisms. Br CI Br Br Br Br RO ROH Н CI н CH, O CH3 „CH3 CH3 -CH3 CH3 н Н но H-o-S-OH
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- For 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 CIHaving trouble carrying out this mechanismConsider the reaction in the box. Which of the following is a key intermediate in the mechanism of this reaction? HO НО OH A) 6 НО НО НО HO НО -OH OH HO OH HO CH₂OH H₂SO4 B) D) НО НО HO HO HO НО OH ОН HO OH HO HO OCH
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- Hello, I am very confused working on this worksheet, please help me understand every step for either reacton or both that I have photos uploaded of!Need help asap thanks!!The reaction below shows a Claisen condensation. O 2 CH3COEt Ethyl ethanoate (ethyl acetate) 1. Eto Na* 2. H₂O, HCI ^nc↔x™ raw curved arrows to show the movement of electrons in the step of the mechanism shown below. Arrow-pushing Instructions :O: O: ·||₂ CH3-COEt + CH₂-COET O CH3CCH₂COEt + EtOH Ethyl 3-oxobutanoate Ethanol (Ethyl acetoacetate) ll.. - :0: :0: || CH3-C-CH₂-C-OEt :OEt A tetrahedral carbonyl addition intermediate