7. Which of the following are intermediates in the oxidation of isopropylbenzene to phenol and acetone? OOH OOH он 1 А 234 12346 с 235 D 136 Е 356
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- If you were using the following reaction to produce acetone (CH3COCH3) CH3COCH2COOH → CH3COCH3 + CO2 what would be the overall atom efficiency of this reactionH3C CH3 H3C NA C→XT Br Br₂ CH₂Cl₂ H3C Electrophilic addition of bromine, Br₂, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH₂Cl₂. CH3 Br In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product with anti stereochemistry is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions Br CH3 H3C CH3问题5 5分 Which of the following describe the major product(s) of this reduction reaction (you may assume excess LIAIH4 is used)? 1. LİAIH4 2. H20 rning primary alcohol secondary alcohol tertiary alcohol aldehyde ketone ester
- The reaction of CH4 and O2 to form C2H6 and H2O must be carried out carefully to avoid a competing reaction. What is the most likely competing reaction?CH3COOH + 2H2 = C2H5OH + H2O %3D Acetate Ethanol Acetate may be hydrogenated to ethanol in industrial reaction systems using several catalysts: Select the most effective catalyst for this reaction system if the free energy of the reaction is -34 kJ/mol; Catalist effective at the temperature range 37-45°C, O Catalist effective at the temperature range 40-55°C, O Catalist effective at the temperature range 60-72°C,Butene (CH2CHCH2CH3) reacts with hydrogen chloride (HCl) at room temperature. Draw the displayed formulae of the products formed in this reaction. State the name of the above reaction mechanism. Alkene Propene reacts with hydrogen bromide (HBr) at room temperature to produce, 1-bromopropane and 2-bromopropane. H2C=CHCH3 + HBr → CH2(Br)CH2CH3 + CH3CH(Br)CH3 Draw out the reaction mechanism of the reaction between propene and hydrogen bromide to produce 2-bromopropane. Use curly arrows to show the movement of electrons. The description should be detailed and must include the type of bond fission that takes place. You may sketch and insert suitable diagrams to aid your description if you wish. Referring to the above mechanism, explain why two products…
- 5. An unknown hydrocarbon A with the formula CóH12 reacts with 1 molar equivalent of H2 over a palladium catalyst. Hydrocarbon A also reacts with OsO4 to give diol B. When oxidized with KMNO4 in acidic solution, A gives two fragments. One fragment is propanoic acid, CH3CH2CO2H, and the other fragment is ketone C. What are the structures of A, B, and C? Write all reactions and show your reasoning.The reaction of ozone with 2-butene leads to -10 formation of aldehyde + ketone 0 aldehyde + alcohol 0 two molecules of carboxylic acid 022. For the reaction between 3-methylpent-2-ene and HBr, which of the following structures correspond to the intermediate(s) and product(s) formed in the major product? 3 28060 Br all will be formed i, ii, iii, iv Br
- The reaction of Hbr with 2-methylpropene produces 2-bromo-2-methylpropane. What is the structure of the carbocation formed during the reaction?A chemist synthesized compound X as a racemic mixture. When the ketone group in X was enzymatically reduced to the corresponding alcohol, a 100% yield was obtained of the product shown below. Choose the statement that best describes this result. ОН enzyme C;H1 `OCH,CH; pH 4.0 C3H1 `OCH,CH3 ОН ÕH X (racemic) (100% yield) One enantiomer of compound X reacts quickly with the enzyme. The other enantiomer of compound X is unreactive, but rapidly equilibrates with the reactive enantiomer under the reaction conditions. Since compound X was racemic, it makes sense that only a single product was obtained. O The product is a meso compound, so either enantiomer of compound X gives the same product. One enantiomer of compound X reacts quickly with the enzyme, while the other enantiomer of compound X remains unchanged.In an advanced synthetic chemistry experiment, a researcher prepares a compound, ZY-7, by reacting a ketone (C5H100) with hydroxylamine (NH2OH), followed by heating in the presence of an acid catalyst. The resulting compound, ZY-7, is then treated with a solution of sodium nitrite (NaNO2) and hydrochloric acid (HCI) at low temperature. Identify the class of compound that ZY-7 most likely belongs to after this series of reactions." A) Amide B) Oxime C) Nitro compound D) Diazonium salt E) Ester Don't use chatgpt please provide valuable answer