Jaslev Propose a synthesis of the following starting from benzene and any other reagents and chemicals. No mechanisms are required. Indicate the condition for each step plus the major product for each step. More than two steps are required. Step 1 Step 2 مہد Br
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- How would you synthesize the followingcompounds from benzene using thereagents from the table? Each requires 3-4steps.The following series of reaction steps will yield 1) But-1-yne plus NaNH2; 2) the product of Step 1 plus Butanone; 3) followed by H30* O 3-methyl-hept-4-yne-3-ol formic acid, propanal and butan-2-ol an octane-based compound containing both a ketone and an alkyne O CO2, propanoic acid and buta-1,2-dione O 4-methyl-hept-4-yne-1-ol QUESTION 34 Which of the following will not oxidize propan-2-ol to propanone? O chromic acid reagent O KMNO4 О МСРВА O nitric acidNonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated , -unsaturated isomers. Propose a mechanism for this isomerization.
- Q24) Provide a synthesis of the following compounds using the given starting material and any other reagents. starting material final product CI starting material final product OH OH OH starting material final product 5) Provide an arrow-pushing mechanism for the following reaction to get to the product shown. HON OH H₂O*, H₂O НО ملهWhat are the products and mechanisms
- 3) Propose a mechanism for the following reaction. HO H2SO4Provide reagents/conditions to accomplish the following transformations. Label each reaction type in the steps you provide. OEt MeO OMeWhat is the product of the following sequence of reactions? D | NaOH NaNH2 H3O+ || ||| explain each steps..explanation needed. don't give Handwritten answer IV NH₂
- Identify the suitable reagents for the given reaction and arrange them accordingly. OH A+&+F OEt 1 2 OEt OEt 1) EtOH, H₂SO4; 2) EtOH, H₂SO4 1) EtONa followed by H₂O; 2) TsCl/py followed by EtONa 1) EtONa followed by H₂O; 2) NaH followed by EtBr O 1) EtOH, H₂SO4; 2) NaH followed by EtBr O 1) EtOH, H₂SO4; 2) TsCmy followed by EtONaIdentify the suitable reagents for the given reaction and arrange them accordingly. 1 OH OEt 2 OEt OEt O 1) EtOH, H₂SO4; 2) EtOH, H₂SO4 O 1) EtONa followed by H₂O; 2) TsCl/py followed by EtONa O 1) EtONa followed by H₂O; 2) NaH followed by EtBr O 1) EtOH, H₂SO4; 2) NaH followed by EtBr O 1) EtOH, H₂SO4; 2) TsCy followed by EtONaThe following nucleophilic substitution occurs with rearrangement as shown below. Suggest a detailed mechanism for the transformation using arrows to detail electron flow.