Give me answer of 4th reaction h- Syl Nucleophilic substitutioni- Sy2 Nucleophilic substitutionj- Electrophilic aromatic substitutiona - Proton transfere - Electrophilic additionb- Lewis acid/basef-E1 Eliminationc- Radical chain substitutiond = Radical chain addition.g- E2 EliminationIdentify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - j for your answers.HIAICI3Cl- AICI,OEtNaOEtOEtHOETNaAIBNCN70°poly(acrylonitrile)(Orlon, Acrilan)

Polymerization reactions are the type of reactions in which a monomer is polymerized to form a…

a - Proton transfer b-Lewis acid base e- Electrophilic addition f-E1 Elimination g-E2 Elimination h- Syl Nucleophilic substitution i- Sy2 Nucleophilic substitution j-Electrophilic aromatic substitution c-Radical chain substitution d = Radical chain addition Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - j for your answers. +] HI AICI, CI-AICI3 OEt Na OEt OEt HOEt Na AIBN CN 70° poly(acrylonitrile) (Orlon, Acrilan)

a - Proton transfer b-Lewis acid base e- Electrophilic addition f-E1 Elimination g-E2 Elimination h- Syl Nucleophilic substitution i- Sy2 Nucleophilic substitution j-Electrophilic aromatic substitution c-Radical chain substitution d = Radical chain addition Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - j for your answers. +] HI AICI, CI-AICI3 OEt Na OEt OEt HOEt Na AIBN CN 70° poly(acrylonitrile) (Orlon, Acrilan)

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter10: Organohalides

Section10.SE: Something Extra

Problem 35AP: Alkylbenzenes such as toluene (methylbenzene) react with NBS to give products in which bromine...

See similar textbooks

Similar questions

a = Proton transfer d = Electrophilic addition g = SN1 Nucleophilic substitution b = Lewis acid/base e = E1 Elimination h = SN2 Nucleophilic substitution c = Radical chain substitution f = E2 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1.fill in the blank 1 2.fill in the blank 2
Using your knowledge of general chemistry and organic chemistry, answer the following questions: Predict the relative acidities within each of the following groups, then identify the conjugate bases, and finally predict their relative leaving group abilities HClO3 and HClO2 PH3 and H2S [NH4]+ and [H3O]+ Explain why the trifluoromethane sulfonate (TfO-) ion is a better leaving group than the methanesulfonate (MsO-) ion.
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.
I. Molecular rearrangementsA) How are 1,2-hydride shifts in carbocation intermediates formed during SN1 or E1-type processes? How are carbocations formed by treating alcohols with water? How can you predict when a hydride shift will occur and how can you show it using arrow-pushing strategies?
In each of the following electrophilic substitution reactions (i) as a first step show the“preactivation” or generation of an electrophilic species; (ii) using arrows provide a mechanisticexplanation of the course of the reaction (show all resonance structures contributing for intermediatearenium ion stabilization); (iii) write all major products of the reaction. Friedel-Crafts acylation of anisole with 2-methylpropanoyl chloride ((CH3)2-CH-COCl) inthe presence of AlCl3 as a catalyst.
Tributyltin hydride (Bu3SnH) is used synthetically to reduce alkyl halides, replacing a halogen atom with hydrogen. Free-radical initiators promote this reaction, and free-radical inhibitors are known to slow or stop it. Your job is todevelop a mechanism,
EFFECTS OF SUBSTITUENTS ON ELECTROPHILIC AROMATIC SUBSTITUTIONA halogen group (-X) is deactivating, what place would it occupy on the following scale? –NO2 > –CN > –SO3H > –CHO > –COR > –COOH > –COOR > –CONH2 > –CCl3 more deactivating less deactivating
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. Discuss the stability of the final compound
Furan undergoes electrophilic aromatic substitution more readily than benzene; mild reagents and conditions are sufficient.For example, furan reacts with bromine to give 2-bromofuran.(a) Propose mechanisms for the bromination of furan at the 2-position and at the 3-position. Draw the resonance forms ofeach sigma complex, and compare their stabilities.(b) Explain why furan undergoes bromination (and other electrophilic aromatic substitutions) primarily at the 2-position.O Br O123furan 2-bromofuran
For the base-catalysed hydrolysis of 3-bromo-3-methylhexane (i.e. reaction with the nucleophile OH-): State whether the reaction is likely to proceed by an SN1 or SN2 mechanism, and explain why give the likely rate law and explain why
Conformation control of reaction mechansims. Consider the reaction below: Provide all possible elimination products from this reaction and identify the major elimination product. Provide mechanisms (with curved arrows) that clearly explain the reaction outcome.
Give 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.