HO OMe 5 6 a. Draw a specific base-catalyzed mechanism. b. Draw a general base-catalyzed mechanism c. Which base would be more likely to exhibit a specific base-catalyzed mechanism, NaOMe or Et3N? Explain your answer in a sentence.
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Consider the formation of lactone (cyclic ester) 6 from 5
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- draw the reaction mechanism.After running various experiments, you determine that the mechanism for the following reaction is bimolecular. CI. + Using this information, draw the correct mechanism in the space below. m Cl. + Ci Add/Remove step Click and drag to start drawing a structure.In an SN2 mechanism, how does it work, what are all of the steps, transition state and all final products?
- H₂C H H₁C Br NBS CH, CH₂ CC, hv **You may assume that Br-Br is formed by a side reaction that occurs (which we discussed in class). This is useful for one of the steps of the mechanism.1. Draw the mechanism for the bromination of ethane. Label steps as initiation, propagation or termination. hv CH3CH3 + Br₂ CH3CH₂Br + HBrAfter running various experiments, you determine that the mechanism for the following reaction is bimolecular. CI <+ + OH + CI Using this information, draw the correct mechanism in the space below. Cl. Add/Remove step X 5 C Click and drag to start drawing a structure.
- From the picture and description can you is that a correct mechanism . can you draw the mechanism ? Phosphate Ester (Minor Product): In the mechanism, a nucleophilic attack by the phosphate ion (�2��4−H2PO4−) substitutes the hydroxyl group in the protonated cyclohexanol. This is a minor product due to steric hindrance. The phosphate group is relatively large and bulky, making the substitution reaction less favored. The size of the substituent may lead to a slower reaction rate and decreased likelihood of successful substitution. Ether (Minor Product): In the mechanism, substitution involves another cyclohexanol molecule attacking the hydroxyl group in the protonated cyclohexanol. Steric hindrance and the availability of a more favorable elimination pathway (dehydration) contribute to the ether being a minor product. The proximity of two cyclohexanol molecules for substitution is hindered by steric factors, making elimination more favorable.Please answer fast I give you upvote1. Answer the following questions on the reaction coordinate diagram pictured below. Reaction Progress a. Label AG on the diagram above. b. Label the reactants, products, transition state(s), and intermediate(s). c. How many steps would the mechanism of this reaction have?