Draw the product of an SN2 reaction shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts. NaSCH 3 TUE Br • Q
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- The reactants, intermediates, final products, and all curved arrows showing bonds forming andbreaking are collectively referred to as the mechanism of a reaction. For the following reactants: a. Explain why the original statement of Markovnikov’s rule does not help in this case, but themodern restatement of Markovnikov’s rule tells you which carbon will get the X (Cl). b. Show the mechanism of the most likely addition reaction between the reactants.Orgonic Chemistry II: The answer is writtten as followed. But I Need Explanation. My question is that: Can I siwtch reagent 2 to reagent 1? for example reagent 1 is Cl2,Fecl3, can I changed it to reagent 2??? Why and why not???A8 Is there anyone who can provide this pericyclic rxn mechanism?
- o chem - please show stereochemistry and break down each step as much as possibleWhat happens to the rate of an SN2 reaction under the following conditions? [RX] is halved, and [:Nu−] stays the same.3) Explain how and why the reaction below results in the observed regiochemistryand/or stereochemistry.
- Rank from decreasing reactive to most reactive (SN1)Add curved arrows to the reactant side of the SN2SN2 reaction shown.1 example of reaction for each of the types of organic reactions: substitution, elimination, addition, and rearrangement. Show:a. the overall reaction (reactants --> products)b. the reaction mechanism (indicate intermediate product)c. indicate which is the reactive species or intermediate in the reaction (radical? electrophile? nucleophile?)d. overall description of the reaction eg., radical substitution or SR