Rank each of the following compounds in decreasing order of reactivity towards Friedel-Crafts alkylation. Most reactive = 1; if a compound will not react, rank it as "non" rather than assigning a numerical value. Compound A: bromobenzene Compound B: aniline Compound C: anisole Compound D: iodobenzene
Rank each of the following compounds in decreasing order of reactivity towards Friedel-Crafts alkylation. Most reactive...
3. Rank the reactivity of the compounds shown below when using a Friedel Crafts alkylation reaction. Make sure you label which is least reactive and most reactive. (5pts)
3. Rank the reactivity of the compounds shown below when using a Friedel Crafts alkylation reaction. Make sure you label which is least reactive and most reactive. (5 pts) 4. Provide a plausible mechanism for the reaction shown.(6 pts) =100
Rank the reactivity of the compounds shown below when using a Friedel Crafts alkylation reaction. Make sure you label which is least reactive and most reactive. (5 pts)
,,,,,,,,,,, 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
Rank the compounds below in order of decreasing reactivity towards electrophilic aromatic substitution Most reactive Least reactive COOH H3C CH3 HOOC- COOH
Rank the following compounds in order of decreasing reactivity in a nucleophilic acyl substitution reactions (most to least reactive from left to right in the answer) yucuruit pun Rank the following compounds in order of decreasing reactivity in a nucleophilic acyl substitution reaction (most to least reactive from left to right in the answer): ei ole C>A>D>B A>C>D>B A>C>B>D C>A>B>D
1. Rank the following carbonyl compounds from 1 to 5 in order of decreasing reactivity towards nucleophilic attack (i.e., from 1 for most to 5 for least reactive). Н Н. OCH I CH3 NO2 CHE CH3 NO2 CH3
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.
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