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- (1, 3) Draw the structure(s) of the major organic product(s) of the following reaction. You do not have to consider stereochemistry. If a compound is formed more than once, add another sketcher and draw it again. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.This question has multiple parts. Work all the parts to get the most points. a Draw all of the monochlorination products that you might obtain from the free-radical chlorination of 2,2,4-trimethylpentane. 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 multiple products using the + sign from the drop-down menu.1) What is the major product for the reaction of 3-bromo1-butene and HBr? Give the name of the product. 2) For this product, how many chiral carbon(s) are there in the structure?3) How many stereoisomers could we write for this product? 4) Write the Fischer Projections of all stereoisomers. (attach a file or other ways you could show your work)
- Compound X is insoluble in cold KMnO4, Br2 in CCl4, and conc. H2SO4. Compound X is most likely: a. an alkane b. none of these c. an alkene d. an alcohol e. an alkyl halide Indicate which of the ff. statements regarding nucleophilicity is incorrect. F- is more nucleophilic, hence, more reactive towards methyl iodide than Cl-. Second row elements are more nucleophilic than first row elements of comparable basicity. The rate of SN2 reaction may be markedly affected by the nucleophilicity of the attacking atom. Nucleophilicity is the affinity of a nucleophile to an electrophilic carbon Which of the following alkynes can be deprotonated by NaNH2 in liquid NH3? 3-Methylhex-2-yne Pent-2-yne 3-Methylbutyne none of these Hex-3-yneC6H5CO2CH2C6H5 can be synthesized by an SN2 reaction. Draw the structures of the alkyl chloride and nucleophile that will give this compound in highest yield. Use the wedge/hash bond tools to indicate stereochemistry where it exists. Include all valence lone pairs in your answer. Separate multiple reactants using the + sign from the drop-down menu. When a metal counterion is needed, use Na+, but draw it in its own sketcher.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?
- Draw the structure(s) of the major organic product(s) obtained after workup of the following reaction. Use the wedge/hash bond tools to indicate stereochemistry where it exists. If no reaction occurs, draw the organic starting material. Draw structure(s) of product(s) after aqueous workup. Include counter-ions, e.g., Na+, I-, in your submission, but draw them in their own separate sketcher. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.Double bonds do not rotate freely under normal conditions. The change from Z to E requires areaction. This can occur in the presence of a catalyst or with the addition of a large amount ofenergy (e.g., at high temperature). One such reaction is diagramed below: (1) Add enough potential energy to break the double bond (Eact) . (2) free rotation occurs at high energy transition state, then (3) reforming the double bond as a mixture of Z and E. Draw E-2-butene in one box and Z-2-butene in the other box, and explain your reasoning.Write out the mechanism for this hydration of an alkene adding curved arrows to show how electrons reorient to make or break bonds or form new lone pairs
- Answer all of question 1 pls 1.i. Give two examples each of Unsymmetrical alkenes and reagents.ii. Give two examples of reactions of alkenes that result in Anti-Markonikov’s addition productsCan someone please explain the logic of 2 vs 3 for stereochemistry? They are both C-C so I don't understand how to rank 2 vs 3. Thank you!lab- oxidation of cyclohexene to adipic acid How do you know the products are purified and how is the identity of the product confirmed? Such as if the product is pure, not pure, or not the desired product?