1. OEt OEt NaBr Na 2. ELOH NaOEt NaCi HOET d = Electrophilic addition g = SN1 Nucleophilic a = Proton transfer substitution h = SN2 Nucleophilic b = Lewis acid/base e = El Elimination substitution c = Radical chain f= E2 Elimination substitution 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. 2. Submit Answer Try Another Version 2 item attempts remaining

1. OEt OEt NaBr Na 2. ELOH NaOEt NaCi HOET d = Electrophilic addition g = SN1 Nucleophilic a = Proton transfer substitution h = SN2 Nucleophilic b = Lewis acid/base e = El Elimination substitution c = Radical chain f= E2 Elimination substitution 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. 2. Submit Answer Try Another Version 2 item attempts remaining

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...

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Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?
Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- ΔH=-75 kJ/mol Rate = k [CH3CH2Br][CH3COO-] Which reaction energy profile would be the best representative of the data provided?
In SN2 reactions of haloalkanes, the order of reactivity is RI>RBr>RCl>RF. Alkyl iodides are considerably more reactive than alkyl fluorides, often by factors as great as 106. All 1-halo-2,4-dinitrobenzenes, however, react at approximately the same rate in nucleophilic aromatic substitutions. Account for this difference in relative reactivities.
i need help filling out the following SN2 reactions with appopiate reactants, products, or reagents,
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Please help me with the organic chemistry problem below: Consider the reaction below: (Check the attached image) (it is between Furan and maleic anhydride, a DIels-Alder reaction) a) Will this reaction for an endo product (with a melting point of 80-81 degrees) or the exo product (with a melitng point of 114 degrees)? b) Carefully explain why the product must have been formed the way it did (exo or endo). c) Provide a mechanism for this reaction.
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