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- Depending on the structure of the organic halide, one or both of these methods may be employed. Complete the following reaction scheme. Part 1- For the given organic halide, select the method(s) that provide the appropriate reagents for steps 1 and 2. Select the single best answer. A. Method 1 only B. Method 2 only C. Both methods 1 and 29. Which reagent/reagents would you use for the following reaction?How does gold help to catalyze the reaction in the gold catalysis experiment? It deprotonates the methanol, making methanol a better nucleophile. оа. o b. It donates electron density to the alkyne, making the alkyne a better nucleophile. О с. It coordinates to the methanol, making methanol a better nucleophile. o d. It coordinates to the alkyne, making the alkyne a better electrophile.
- 3. Show two different ways you would make 3-methyl-3- hexanol via a Grignard reagent, beginning each time with any alkyl or aromatic halide, and any other organic and inorganic reagents.In the reaction series below, write down the appropriate reagents that can be used where there are question marks.6. Multi Step Synthesis. Propose a synthetic route from the reactant to the product using any reagents you need. Nalt LINH4
- True or false 1.Hydroxide is the good leaving group for SN2 reaction. 2.Iodide ion is the better leaving group than the bromide ion. 3.Ethyl bromide is the better substrate than t-butyl bromide for SN2 reactions. 4.water is the protic solvent. 5.Sn1 reactions take place in one single step.Fill in the reagents below/above the arrow in the ff reactionI need help with the ones that are circled. Looking for the reagents necessary for the following transformations. Thank you