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- Draw eugenol as a line structure. The double bonds of the benzene ring are fairly unreactive unless you use special catalysts. But the double bond on the side group is reactive. Draw the mechanism of eugenol reacting with HBr to form the two possible carbocation intermediates. Put your intermediates into square brackets. Label each carbocation as a methyl carbon or 1°, 2°, or 3°. Then circle a more stable carbocation if one is more stable. Can you guess what the final product is?Q: Provide the reagents needed to carry out the reactions below (or the product obtained). If two steps are needed, clearly indicate 1. (reagent A); 2. (reagent B). If separate steps are not indicated, I will assume you mean that all reagents are introduced together. Will H20 and H30+ work if so can you explain how for this question I am working on 2EDraw the product of an SN2 reaction shown below. Use wedge and dash bonds to indicate stereochemistry where appropriate. Ignore inorganic byproducts.
- Fill in the information based on the type of reaction mentioned in each column. A. Draw the line angle diagram of a substrate that will undergo SN1, SN2, E1, E2 B. Draw the line angle diagram of a nucleophile that can be used for SN1, SN2, E1, and E2 C. Draw the line angle diagram of a solvent that can be used with SN1, SN2, E1, and E2 D. Write down if the stereochemistry of the product will be inversion, retention, or a 50:50 ratio of inversion and retentioni. Fill in the missing starting materials, products, or reagents as necessary. ii. Label each transformation as SN1, SN2, or acid/base. iii. Indicate if the product is racemic or a single enantiomerComplete the reactions below using the required reagents or products. If there is no reaction, indicate so. If a product is in the majority, specify which one.
- Rearrangements can occur during the dehydration of 1° alcohols even though no 1° carbocation is formed—that is, a 1,2-shift occurs as the C— OH2+ bond is broken, forming a more stable 2° or 3° carbocation, as shown in Equation [1]. Using this information, draw a stepwise mechanism for the reaction shown in Equation [2]. We will see another example of this type of rearrangement in Section 16.5C.Several reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.What are ALL of the products of buta-1,3-diene and bromine water? I know how to get to the major product (bromine and OH both to the left of the double bond) but don't know how to get to the minor product (bromine to the left, OH to the right)?
- 1.) Can you draw this out in more detail and explain the FC alkylation 2.) I do not understand what it is asking 3.) Can you confirm if it is correct or notDraw the organic product(s) of the following reaction. You do not have to consider stereochemistry. Include cationic counter-ions, e.g., Na+ in your answer, but draw them in their own sketcher. If no reaction occurs, draw the organic starting material. Separate multiple products using the + sign from the drop-down menu.Rearrangements can occur during the dehydration of 1° alcohols eventhough no 1° carbocation is formed—that is, a 1,2-shift occurs as the C—OH2+ bond is broken, forming a more stable 2° or 3° carbocation, asshown in Equation [1]. Using this information, draw a stepwisemechanism for the reaction shown in Equation [2]. We will see anotherexample of this type of rearrangement