Place the following in order from least reactive to most reactive, in reference to reactivity towards...
Rank the compounds below in order of decreasing reactivity towards electrophilic aromatic substitution Most reactive Least reactive COOH H3C CH3 HOOC- COOH
,,,,,,,,,,, Rank the compounds below in order of decreasing reactivity towards electrophilic aromatic substitution. Most reactive Least reactive COOH H3C CH3 COOH HaC
Rank the monosubstituted benzene compounds below in order of decreasing reactivity towards electrophilic substitution. Most reactive Least reactive
Can someone explain how I am supposed to know which is least reactive compared to most reactive? I know that the benzene with the NO2 group on it is least reactive because it's an EWG (electron withdrawing group) so a deactivator but how do I compare the others? Thanks!!! Rank the following compounds in order of their reactivity toward electrophilic aromatic substitution NO2 CH least reactive (slowest) most reactive (fastest) b Rank the following compounds in order of their reactivity...
20) Rank the following Carboxyllic Acid derivatives in decreasing order (Most to Least) of reactivity towards Nucleophillic Substitution reactions? 3 Pts "NH2 II III IV More Reactive: Least Reactive 21) Match the following? 2 Pts 1) Alkynes 2) Aromatic Compounds 3) Aldehydes/Ketones 4) Carboxyllic acid derivatives A) Nucleophillic Addition Reactions B) Nucleophillic Substitution Reactions C) Electrophillic Additon Reactions D) Electrophillic Substitution Reactions
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution Most reactive acetyl chloride hexyl propanoate Least reactive acetic anhydride propionamide
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic attack. Most Reactive to least reactive. 3-methylpentanoyl chloride, acetic anhydride, hexyl propanoate, N,N-diphenylethanamide, butanedial, and propanone.
Arrange the following groups of compounds in order from most reactive to least reactive toward electrophilic aromatic substitution. 1. Benzene, ethylbenzene, chlorobenzene, nitrobenzene, anisole. 2. Toluene, p-cresol, benzene, p-xylene. 3. Benzene, benzoic acid, phenol, propylbenzene. 4. p-Methylnitrobenzene, 2-chloro-1-methyl-4-nitrobenzene, 1-methyl-2,4-dinitrobenzene, p-chloromethylbenzene.
In the following compound, select the position that is most reactive towards electrophilic aromatic substitution reaction. Review of Skills - Skill Builder 18.03 X Incorrect. Tert-butyl (activator) will direct the incoming electrophile and it is an ortho-para director. In the following compound, select the position that is most reactive towards electrophilic aromatic substitution reaction. NO,
rank the following compounds on the basis of reactivity toward electrophilic aromatic substitution use 1 for most reactive and 4 for least Provide the major enolRank the following compounds on the basis of reactivity toward electrophilic aromatic substitution use 1 for most reactive and 4 for least