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.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.