39. Which product(s) will be isolated from the reaction shown here? Br A. CH3CH₂O Na* CH3CH₂OH B C) Equal amounts of A and B. D) Neither A nor B.
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- [VI9] Instructions: Provide the missing reagent/s, substrate/s, or product/s for each reaction. (refer to the photo below)Draw the final product formed in the reaction below.What kind of reagent is KmnO4? Draw the possible reactions of this reagent with the specific compounds tested in the following reaction?
- The use of curved arrows is a powerful tool that illustrates even complex reactions. a.Add curved arrows to show how carbocation A is converted to carbocation B. Label each new σ bond formed. Similar reactions have been used in elegant syntheses of steroids. b.Draw the product by following the curved arrows. This reaction is an example of a [3,3] sigmatropic rearrangement, as we will learn in Chapter 25.Which mechanism gave the main product in the reaction shown in Figure 8? * A- SN1 B- SN2 C- E1 D- E2Draw the products of each reaction. Assume excess halogen is present.
- Rank the nucleophiles in each group in order of increasing nucleophilicity. a.−OH, −NH2, H2O b.−OH, Br−, F− (polar aprotic solvent) c.H2O, −OH, CH3CO2−4. Identify the reagents (a–h) needed to carry out each reaction. Provide an explanation to your answer. (see attached photo)1.Label kinetic product 2.Label the thermodynamic product 3.Predict the four products from reaction of alkene with one equivalent HBr
- Which compound reacts fastest in an E1 rxn. The correct answer is C but explain why it is correct and why the other options are incorrect. thanks :)What starting materials are needed to prepare each compound using a Heck reaction?In the box to the left of each reaction below, write the mechanism by which it occurs (could be SN1, SN2, or E1, or even 2 of them). Then draw the product(s). i need H and M done