your mechanism explains the stereochemical outcome. CI Problem 11: Use mechanism to predict the product of the following reaction. Be sure that Cl2 enantiomer I Н.0 'Cl +
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- Can someone explain to me the mechanism for the reaction? I don't know what type of reaction this is and how they add together to create the product. I do understand the actual product is correct because having all substituents equitorial is favorable.A student proposes the following reaction mechanism for the reaction in Model 6. Which step inthis mechanism is least favorable? Explain your reasoning.What are the major product(s)? Show the mechanism.
- Is this mechanism Sn1, Sn2, E1, or E2This is the feedback I'm getting: This reaction is an SN2 reaction. With the epoxide above the plane of the ring, the ethoxide will attack the lower face of the ring, producing a product with a trans orientation. Consider if the product(s) will have zero, one, or two chirality centers.Can you answer the question and show the mechanism and explain it? And one more thing how do I know when a reaction is not going to react in the case of sn2 sn1
- Draw mechanism arrows and then predict the major products and stereochemistry. Also include the labels of thermodynamic and kinetic 4-methylocta-2,4-diene with Br2 in CCl4Draw the mechanism of the following reactions and the corresponding products. Pay attention to the stereochemistry. For both reactions, do you decide whether they are SN1- or SN2-likeDraw mechanism arrows and then predict the major products and stereochemistry. Also include the labels of thermodynamic and kinetic - no stick structure please dont understand like that. - 4- methypenta-1,3- diene with Hbr