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Q: Identify the stronger nucleophile in the following pair of anions. Br− or Cl− in a polar protic…
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A: See answer below.
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Q: How might nucleophilic catalysis work? Draw out a possible mechanism.
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Q: Question attached
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Q: final
A: Please find the file attached for explanation
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A: Intramolecular attack of OH to give a cyclic product shown below.
Q: Rank the nucleophile strength of the structures from weakest to strongest.
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Q: then
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- Explain how you can tell from the energy diagram that the reaction with the catalyst in Fig. 8.4 isfaster than the reaction without the catalyst.6. Place an "X" in the box below the nucleophile that will react the most quickly with methyl iodide. Place an "O" in the box below the nucleophile that will react the most slowly with methyl iodide.Consider this nucleophilic substitution reaction. 1. Highlight the electrophilic carbon in red, and highlight the leaving group in blue. Highlight the atom in the nucleophile that will attack the electrophilic center in green. Only atoms need to be highlighted and not the lone pairs or formal charges. 2. Draw the product(s) of the reaction. Include all lone pairs.
- How might nucleophilic catalysis work?Draw out a possible mechanism.1. Attack the alkyl chloride with the stronger nucleophile. 2. Deprotonated to form the product3. Does it matter what order you mix the reactants together in? If so, what is the correct order? 4. During the reaction, when do you start the timer? 5. How will you know when to stop the timer?
- Nucleophilicity is a kinetic property. A higher nucleophilicity indicates that the nucleophile will easily donate its electrons to the electrophile and that the reaction will occur at the faster rate. The reaction rate also depends on the nature of the electrophile and solvent. Rank the following reactions from fastest to slowest based on the nucleophilicity of the nucleophile. Rank from fastest to slowest. To rank items as equivalent, overlap them.Which is/are NOT TRUE about bimolecular nucleophilic substitution reactions? Select one or more: 1. A carbocation intermediate is formed. 2. A strong nucleophile displaces a halogen atom in a concerted mechanism. 3. Presence of polar aprotic solvents promotes this reaction. 4. Methyl halides react faster than secondary alkyl halides.This is a umplong reaction. I'm looking for what reagent and intermediates would look like. Thank you