Q: (1) Mg dry THF Br (2) H3O*
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A: Given: The product for given reaction is determined as shown below,
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A: The organic products can be shown below,
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A: Given:
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Q: Draw the organic product(s) of the following reaction. aqueous H2SO, NaCN
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Q: What starting material is needed to synthesize each compound by a ring-closing metathesis reaction?
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Q: Draw the organic products formed in attached reaction.
A: Lithium aluminium hydride (LiAlH4) is a strong reducing agent
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Q: pH 4.5 H,C. `CH, + *CH3 `NH,
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Q: 8. Draw the structure of the product of the reaction displayed. 1) ВН:THF 2) H2O2, OH
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Q: Draw the structures of the neutral organic products formed in the following reaction. Do not draw…
A: Please find below the mechanism for the reaction taking place.
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- C6H5CO2CH2C6H5 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 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.(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.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?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)
- - For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H2SO4H2SO4, then draw the structure of the major product of the elimination. (Picture 1): Step 1: Use curved arrows to complete the protonation mechanism of the alcohol. Step 2: Use a curved arrow to show the formation of the carbocation intermediate. Note: HSO−4HSO4− is formed from step 1, but not shown. (Picture 2): Step 3: Use a curved arrow to show the carbocation rearrangement. Step 4: Draw curved arrows to show the elimination to form the major product. Water is added as a base. - Draw the major product of the elimination. H3O+H3O+ has been pre‑drawn for your convenience.A. Without the use of H2 reductions or PCC oxidation fill in the blank steps of the reactions. Final products should be the major organic product.Fill in the missing information (reactants, products, or reagents) in the following transformations. If more than one product is possible, draw structures for all products and indicate the major product. If stereoisomers are possible, draw all isomers, and indicate the major stereoisomers.
- Curved arrows are used to illustrate the flow of electrons. Follow the arrows to predict the reactant and product of reaction. Include all lone pairs. Use wedges and dashes to indicate stereochemistry. Ignore inorganic byproducts.Start with condensed structural formula CH3-CH(OH)-CH(CH3)-CH2-CH(CH3)2 and react it first with H2SO4 and high heat, to produce a major substrate product. Then, take that major substrate product, and use it as the substrate of the next reaction, by reacting it with Br2 (in the presence of CH2Cl2 solvent), to produce the FINAL MAJOR substrate product. The complete correct condensed structural formula for the major substrate product after reaction step 1 is ___________. (If no new product is formed in this step, type "no reaction.") The complete correct condensed structural formula for the final major substrate product (after reaction step 2) is __________ . (If no new product is formed in this step, type "no reaction.")You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. Do not include lone pairs in your answer. Draw phosphate groups, when present, as in the question: in basic form and with a phosphorous oxygen double bond.