There are TWO reactions that will happen when we react the molecule shown below with methanol under acidic conditions. Predict the product( s) and show the FULL mechanism methanol, HCI (cat)
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A: [HF][H3O+][F−]=Ka Explanation:
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Q: 5. Complete the following table. Functional Group Name Sample Functional Group Naming Rule
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Q: Question is in attached image
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A: Given:We have to find the IUPAC name of the compound
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- It is not uncommon for organic chemists to prepare acetals by an exchange-type process known as transacetalization. Predict the product(s) and show the mechanism for the transacetalization reactions below.[Rh(PPh3)3Cl] is a precatalyst that can be activated by dissociation of a phosphine ligand to form an active catalyst, B, which is used in the hydrogenation of alkenes. The active catalyst can then undergo oxidative addition in the presence of H2 to form complex C. Propene coordinates to C to form complex D, which then undergoes a 1,2- insertion step to form E. Reductive elimination of propane from E regenerates the active catalyst B. Draw complexes B – E and hence provide a full catalytic cycle, including the activation step, for the hydrogenation of propeneThe following halide reacts differently with hydrogen sulfide as shownshown in the attached image reactions. For each reaction, show the mechanism, draw the energy diagrams for the formation of each product and write the rate equation for the formation of each product. PD: mechanisms are SN1,SN2,E1 etc
- For each reaction below, provide the structural formula for the reactants and the predicted products. Indicate which mechanism the reaction will follow and use curved arrow formalism to illustrate the predicted reaction mechanism. t-butylalcohol + NaBr ?The following alcohols react with HBr to afford an alkyl bromide. Based on their structures, indicate if the reaction mechanism is likely to be Sn1 or Sn2Chemistry III. reactionsGive the main product and specify the mechanism that is favored.
- The reaction below may be made to proceed rapidly by the following changes, except:The reaction between peroxodisulphate (VI) ions, S2O82- and iodide ions, I- can be catalyzed by iron(III) ions, Fe3+. Suggest a mechanism for the catalytic reaction.Choose the correct steps in the dehydration of secondary alcohol; then, arrange inchronological order.I - Formation of AlkeneII - Formation of AldehydeIII - Formation of Protonated alcoholIV - Undergoes E2 mechanismV-Undergoes E1 mechanismA. V-III-IB. IV-III-IIC. III-V-ID.III-IV-II Ethanol is heated with an acidified potassium manganate (VII) solution. What would be theproduct of this reaction?A. EthanalB. EtheneC. Ethanoic acidD. Ethane ALL of the following Ether can be prepared by Williamson's method, EXCEPT:A. Ditertbutyl etherB. Ethyl-tert-butyl etherC. anisoleD. Both A & B. Which of the following is not true of SN1 reactions?A. They are favored by nonpolar solvents.B. The concentration of nucleophiles does not affect the rate of reaction.C. Tertiary alkyl halides generally react through this mechanism.D. They occur through a 2-step concerted reaction. Butan-1-ol is formed from which of the following reactant-reaction pairs?A. Butanal - reduction reactionB. Butanone -…
- Two chemists at Dupont found that ICH2ZnI is better than diazomethane at converting a C=C bond to a cylcopropane ring. Propose a mechanism for the reaction, now known as the Simmons–Smith reaction in their honor.Acetic anhydride reacts with water in the following manner: CH3C(O)-O-C(O)CH3 + H2O = 2CH3CO2 If this reaction is carried out in an inert solvent with low concentrations of both acetic anhydride and water, it follows the rate law rate = k [CH3C(O)-O-C(O)CH3] [H2O] with a rate constant of 0.0035 s-1. However, if low concentrations of acetic anhydride are placed in pure water, it follows the rate law rate = K [CH3C(O)-O-C(O)CH3] where K = 0.1944 s-1. Explain why this is happening.Predict the products by showing the reaction mechanism (arrow pushing) of the given diagram.1. MCPBA; H3O+ 2. O3; DMS 3. H3O+