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- Illustrate the resonance effect of the methoxy group -OCH3, on the structure of the benzene ring. Draw all the oissuvke resonance forms of methoxybenzene, including the hybrid Based on the structures, explain how the presence of the -OCH3 group affects: (i) the reactivity of the benzene ring towards electrophilic attack (ii) the orientation or point of attack of an incoming electrophilic reagent on the benzene ring.1.) Predict the reactivity of the following alkyl bromides in a substitution reaction with NaI in acetone. Rank them from 1-2 with 1 being the fastest and circle the molecule(s) that reacted in the substitution experiment? 2.) Rank the molecules from 1-2 based on their rate of reactivity with NaI with 1 being the fastest. Explain the theory behind your ranking of each compoundHelp ASAP Illustrate the resonance effect of the methoxy group -OCH3, on the structure of the benzene ring. Do this by writing all the possible resonance forms for methoxybenzene, including the hybrid. Based on your structures, explain how the presence of the -OCH3 group affects: (i) the reactivity of the benzene ring towards electrophilic attack; (ii) the orientation or point of attack of an incoming electrophilic reagent on the benzene ring.
- Choose the best reagents from the list provided below for carrying out the following conversion. Match the reagent with the step number. HCl (aq), Zn(Hg) KMnO4, H3O+ CH3Cl, AlCl3 HNO3, H2SO4 Cl2, FeCl3 fuming sulfuric acidGive a detailed mechanism including all resonance isomers for intermediates (show electron flow) for the Friedel-Crafts reaction Expt. 29.4-micro: Friedel-Crafts Synthesis of 1,4-t-Butyl-2,5-dimethoxybenzene. NOTE: It is likely the mechanism from reactants to only 1-t-butyl-2,5-dimethoxybenzene. I want a complete mechanism showing all steps and resonance isomers for the synthesis of the dialkylated product.Give a detailed reaction mechanism for the reaction expected to occur when 2-bromo-2-methylpentane is heated with sodium methoxide. Draw clear structural formulas of all relevant species and use curved arrows to represent electron flow. Also indicate which step is likely to be rate-determining. The answer you sent before will be used for this question.
- Draw the major and minor product that could be formed when 1-methoxy-1,3-butadiene reacts with 2-methylpropenoic acid. Ignore any stereochemistry. Show your work.(UV spectroscopy lab, organic chem 2) Perhaps it is unsurprising that cyclohexane and ethanol are reasonable UV solvents, whereas toluene is not. Explain why that is. please answer, in detail- will give a thumbs up. thank youONLY USE THINGS LEARNED IN ORGANIC CHEM 1 Show stepwise mechanism by pushing arrows (Fishhook) and drawing all intermediates: Draw a detailed mechanism for the addition of HBr to 3,3-dimethyl-1-butene in the presence of dimethylperoxide. Show and label all steps including initiation, propagation and termination.
- What is the detailed reaction mechanism between 1-indanone and veratraldhyde, with a NaOH base and no solvant? The final product should be 2-(3,4-dimethoxybenzylidene)-1-indanone. Please include arrows and charges. Thank you.Provide the mechansim using curved arrows of the reaction of p-t-butyl phenol treated with acetic anhydride in AlCl3. Include resonance stabilized intermediates and if more than one product is formed, label them as major, minor, etc. thank you for the helpCan someone please help me with 2 mechanisms? One is for the synthesis of 1-bromobutane, and the other is for 2-bromobutane. The attached reaction shows the reagents and starting product.