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- Give the reaction mechanism for the following subparts in clear handwritten!The following chemical transformations involve multistep mechanisms. Please write a reasonable mechanism for each transformation and label each elementary step.) Fill in the red box(es) with the missing reactant(s), reagent(s), product(s), solvent, and/or conditions and write a reasonable mechanism for the reaction. Not every box needs to be used and not every box necessarily corresponds to only a single species. If no reaction occurs OR no reagents exist to perform the reaction state, "NOT POSSIBLE" AND explain why. =. OH OH
- 2- Write step-by-step mechanism for the following reaction: Cul R1 но .*...... ....... ........The following compounds are major products of an elimination reaction with an alkyl halide. Determine the structure of the alkyl halide and write the overall reaction mechanism. Determine the minor and major products.Examples of E1 and E2 reaction mechanism.
- The following mechanism has been proposed for the reaction of NO w/H2 to form N2O and H2O NO(g) + NO(g) --(k1)--> N2O2 (g) N2O(g)+ H2(g) --(k2)-->N2O(g)+H2O(g) a. Show that the elementary steps of the proposed mechanism add to provide a balanced equation for the reaction b. Write a rate law for each elementary step in the mechanism c. Identify any intermediates in the mechanismFill in the red box(es) with the missing reactant(s), reagent(s), product(s), solvent, and/or conditions and write a reasonable mechanism for the reaction. Not every box needs to be used and not every box necessarily corresponds to only a single species. If no reaction occurs OR no reagents exist to perform the reaction state, “NOT POSSIBLE” AND explain why.The following compounds are major products of an elimination reaction with an alkyl halide. Determine the structure of the alkyl halide and write the overall reaction mechanism.
- In an SN2 mechanism, how does it work, what are all of the steps, transition state and all final products?For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be true for one or moremechanisms. The reaction rate increases when the solvent is changed from CH3OHto (CH3)2SO.Sketch the reaction mechanism (including the final product) corresponding to the following description of; 2-bromo-4-methylpentane is being reacted with sodium cyanide in diethyl ether (set up the reaction – next you will get a description of the mechanism to draw). A lone pair of electrons from the cyanide attacks the carbon bonded to bromine, forming a new carbon-carbon bond. At the same time, the carbon-bromine bond breaks with the electron pair from the carbon-bromine bond moving toward the bromine to form a bromide ion. This will form the product 2,4-dimethylpentanenitrile and sodium bromide.