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- Use the dropdown menu to indicate whether the rate of the reaction shown below will increase, decrease, or remain the same when the reaction conditions are changed to X or to Y or to Z (see below). NaCN Br CN CH3CN X: Change the leaving group from Br to CI Y: Increase the concentration of haloalkane Z: Increase the concentration of NaCN X: choose your answer... Y: choose your answer... Z: choose your answer... >3. Draw the reaction mechanism for the following reactions. When possible, label nucleophiles/electrophiles, carbocations, and oxonium ions. H* CI. a) H. + H2O + НОCHЗ H* OH H* H;CPart B?
- Use the dropdown menu to indicate whether the rate of the reaction shown below will increase, decrease, or remain the same when the reaction conditions are changed to X or to Y or to Z (see below). NaN3 'N3 Br CH3CN X: Change the leaving group from Br to CI Y: Increase the concentration of haloalkane Z: Increase the concentration of NaN3 X: choose your answer.. ^ Y: choose your answer... V Z: choose your answer... choose your answer... Remain the same Nex Decrease IncreaseOf the following halonium (bromonium) ions; Indicate for each one which of the two carbons is more susceptible to being attacked by the nucleophile and explain why. Br+ Br* Br Br X X CH3 CH3 H CH3 H |||4 H H3C... H 114 H H1. Reaction mechanism and alkebe product 2. Major product
- Please help me with both of these problems, they are the same question its just a two-part, I really want to study so please helpPlease help, I answered it wrong.H3C OH OH CH3 1,3-pentanediol + B OMe OME OME MeO... CH3 H3C OMe benzaldehyde dimethylacetal catalytic Me 0:0 OH FO (p-TsOH) CH3CN H... MeO, OMe OMe e a & H3C CH3 H3C CH3 H3C CH3 C D A HO E HO OCH3