7. Draw the mechanism to describe the following transformation: Note: This is a base catalyzed reaction. So, the last steps must make [OH]- OH [OH]¯ OH Heat O
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![7. Draw the mechanism to describe the following transformation:
Note: This is a base catalyzed reaction. So, the last steps must make [OH]-
OH
[OH]¯
OH
Heat
O](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F388c6efd-de98-4f85-9159-4606d7c40ad8%2F5919ae53-7ef4-4056-afc9-f294eda689cb%2F2mkhejz_processed.jpeg&w=3840&q=75)

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- Rank the following bases in order from slowest E2 reaction rate to fastest. ONa H20 NaOH NH3 OK ONa A В D E FA H2N. Figure 9: Multi-step reaction sequenceDraw the mechanism for the reaction of an alkyl halide with sodium azide followed by reduction. Complete the mechanism of the initial step of the reaction, then identify the key intermediate and the product. Step 1: Draw curved arrows. o z + Na + || : z: I Step 2: Complete the intermediate. Na +
- Draw a detailed, step-wise mechanism for the reaction shown below. SHOW ALL BOND-FORMING AND BOND-BREAKING STEPS. SHOW ALL INTERMEDIATES. 1) NaOH 2) H3O* H3C H3C HO6. Predict the reactant (starting material) for the reaction and propose a mechanism. NaCN SN2 NaOH E2 CN a Ph PhA set of three nucleophilic displacement reactions is shown below: - Br -Br -Br "CHз Hзс CHз C В A NaCN CH-он SN2 reaction Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest?
- The following transformation can be accomplished by reactions we have studied in this chapter and Chapter 20. Name the type of reaction used in each step.5. Which one of the following ions/molecule is the strongest nucleophile? CH -SH A В E5. The reaction below proceeds through a 4-step mechanism. Classify each step according to the pattem(s) of arrow-pushing (nucleophilic attack, loss of a leaving group, proton transfer, rearrangement). Please provide curved arrows for each step. Pinacol Reaction OH OH Mechanism: Step 1: Step 2: Step 3: Step 4:
- This reaction is an example of conjugate addition of a nucleophile to an a,ß-unsaturated carbonyl. LOCH3 H20 H3C H3C° OCH3 OCH3 Draw the two resonance structures of the enolate anion intermediate for this reaction.Br CH3OH + Br-Br H3CO The mechanism proceeds through a first cationic intermediate, intermediate 1. Nucleophilic attack leads to intermediate 2, which goes on to form the final product. In cases that involve a negatively charged nucleophile, the attack of the nucleophile leads directly to the product. +Br + CH3OH Br Intermediate 1 Intermediate 2 (product) In a similar fashion, draw intermediate 1 and intermediate 2 (final product) for the following reaction. OH + Br2 + HBr Br racemic mixture • Pay attention to the reactants, they may differ from the examples. In some reactions, one part of the molecule acts as the nucleophile. • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate intermediate 1 and intermediate 2 using the → symbol from the dropdown menu.All I need help with, is everything about this process, please send help!



