redict the major products of this organic reaction: AICI3 ? ote for advanced students: you may assume that an excess of benzene is used as part of the reaction conditions. Check X
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- In the reaction from compound 10 to compound 11, why the C=C bond is retained and is not hydrogenated? f) LiAlH4, Et2O, 08C; g) Ac2O, py, DMAP, CH2Cl2, RT, 77% over 2 steps;Organic Chemistry: 1) 2-Butanol heated with KMnO4 will produce 2-butanone 2) 2-Propanol heated with concentrated H2SO4 will produce 2-propanone? Can I have the equation :( I need to check my workHow do I calculate the percent yield based on the limiting reactant in this bromination of trans-cinnamic acid reaction? (See attachments for further information)0.149 g of trans-cinnamic acid was initial mass of the alkene 1.0 mL of glacial acetic acid (AcOH) was used 1.0 mL of Br2 was used 0.128 g of (2R, 3S)/(2S, 3R)-2,3-dibromo-3-phenylpropanoic acid was the final mas of the product
- How can you analyze or characterize a final product? What analytical techniques you can use to check the formation of the final product?2 Organic Synthesis! Palladium catalyzed reaction. Complete the reaction! Please only answer if you are 100% sure! Thank you in advance!Organic Chemistry Please help with finding the product of this reaction. Thank you
- Complete and balance the following methesis reaction in aqueous solution.Answer Entery Instructions• Parentheses are only required around polyatomic ions and only when more than 1 of those ions is present.K3PO4 (no parentheses required).Mg3(PO4)2 (parentheses required).• In each case one product is soluble (aq) and one insoluble (s). Use solubility rules to determine which product appears in each box.***Answer*** Na2S (aq) + ***Answer*** FeCl3 (aq) ➝ ***Answer*** ***Answer*** (s) + ***Answer *** ***Answer*** (aq)The addition of an alcohol to an acid chloride is an example of alcoholysis (alcohol addition with bond breakage). Consider the alcoholysis reaction below and answer the questions that follow. 1. Show the tetrahedral intermediate that is formed after the nucleophilic addition of the alcohol to the acid chloride. Be sure to include all lone pair electrons and formal charges on your intermediate structure. 2. Show the final product of this alcoholysis reaction that forms after the intermediate you made in Part 1. Do not include inorganic or charged products in your answer. Be sure to include all lone pair electrons and formal charges.Phineas and Ferbs, two brothers who enjoy vacations, doing fun things every summer. This summer the brothers and their friends carry out an organic synthesis with an unknown compound (L1) that contains 52% Carbon, 6% Hydrogen and 42% bromine, this compound (L1) is treated with magnesium in ether to obtain L2 , which reacts violently with D2O for 1-methyl cyclohexene with a deuterium atom in the methyl group (L3). The L2 reaction is treated with acetone followed by hydrolysis to give L4. Heating L4 with concentrated sulfuric acid gives L5, which decolors the bromine, obtaining L6. L5 undergoes hydrogenation with excess hydrogen and platinum as a catalyst giving rise to isobutyl cyclohexane. Determine the structures of compounds L1 through L6.
- This image is the final product that is produced. If a synthesis started with benzene and other organic compounds (four carbons or less) what would the synthesis look like to achieve this final product.Please show the steps to the organic synthesis reactions below:Solve for the starting material or product and then fill in the missing componenet to give overall reaction. Use one of this reactions I) CH3OH/H2SO4 2) 1. BH3. 2. H2O2, OH,H20 3) 1. OSO4. 2. NaHSO3 4) H3O+ 5)1. Hg(OAc)2, CH3OH. 2. NaBH4 6) Br2 in CCL4 7) Br2 in CH3OH 8)Br2 in CH3OH 9) Cl2 in H2O Show reaction mechanism
