The herbicide oxyfluorfen can be prepared by raction between a phenol and an aryl fluoride. Propose a mechanism. CH2CH3 кон NO2 Он `CH2CH3 NO2 Oxyfluorfen
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- Draw the products formed when each compound is treated with HNO3 and H2SO4.State whether the reaction occurs faster or slower than a similar reaction with benzene.b) The Wolf-Kishner reduction is a reaction used in Organic Chemistry to convert carbonyl functionalities into methylene group. The reaction was used to convert an aldehyde or ketone to an alkane using hydrazine, base and thermal conditions. The mechanism begins with the attack of hydrazine of the aldehyde or ketone. Stage 1: The reaction of aldehyde/ketone with hydrazine to produce hydrazine Stage 2: Reaction with the base and heat to convert hydrozone to alkane Write the mechanism of the reaction.Acetic acid has been mixed with isoamyl alcohol to produce isoamyl acetate giving off a banana smell. Propose a reaction mechanism for this reaction.
- Acetals are formed from the reaction of two alcohols with a carbonyl under acidic conditions. Acetal formation is faster with 1,2-ethanediol than with two methanol molecules. Choose the factor that explains the difference in reaction rates. A) The reaction with 1,2-ethanediol has a lower AH (enthalpy) of reaction. B) The reaction with 1,2-ethanediol has a higher AH (enthalpy) of reaction. C) The reaction with 1,2-ethanediol has a more favorable entropy of reaction.How does propane synthesized from propanone? Show its mechanism.Complete the following reactions by filling in any missing reactants, reagents or products. a) Zn(Hg) conc. HCl b) ОН ? с) ОН РСС CH,Cl,
- Identify the best reagents to complete the following reaction. Options are included.The reaction of an alkene with diazomethane forms a cyclopropane ring. Propose a mechanism for the reaction.What is required to complete the following reaction? H3C H 1) CH3CH₂MgBr, ether 2) H3O+ 1) LDA, THF 2) CH3CH₂Br 1) NaOH 2) CH3CH₂MgBr, ether 1) CH3CH₂Br 2) H3O+ H3C H₂ H
- Propose a mechanism for the reaction of benzyl acetate with methylamine. Label theattacking nucleophile and the leaving group, and draw the transition state in which theleaving group leaves.1. Draw the products for the following substitution reactions: benzylbromide LDA, THE benzylbromide NaOCH3 MEOH benzylbromide LDA, THE benzylbromide NaOCH3 MEOHShow two reaction schemes to synthesize the following compounds. Pick one reactionscheme and draw the step-by-step reaction mechanism