Rank all of the carbonyl-containing compounds in Figure 1 in
terms of most electrophilic (4) to least electrophilic (1).
phenyl benzoate
benzanilide
benzophenone
2-naphthaldehyde
Rank all of the carbonyl-containing compounds in Figure 1 in terms of most electrophilic (4) to...
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic attack. Most reactive acetyl chloride propionamide benzoic anhydride isopropyl benzoate acetaldehyde propanone Least reactive
Rank the following carbonyl-containing
compounds in order of reactivity towards nucleophilic acyl
substitution.
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution Most reactive Least reactive butyl acetate benzoic anhydride 3-methylpentanoyl chloride propionamide
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.
Rank the following carbonyl-containing
compounds in order of reactivity towards nucleophilic
attack.
Rank the following carbonyl - containing compounds in order of reactivity towards nucleophilic attack.
Rank the following carbonyl-containing compounds in order of
reactivity towards nucleophilic attack.
draw theproducts of the following reaction as they occur in acid
solution.
Classify these structures as hemiacetal, hemiketal, acetal,
ketal, or other.
Draw the final organic product of the following three-step
reaction of bromomethylbenzene.
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic attack. Most reactive Least reactive acetic anhydride methanal propanone butyl acetate N,N-diphenylethanamide 3-methylpentanoyl chloride
3. Rank the following carbonyl compounds most reactive (label as 1) to least reactive (label as 4) to nucleophilic acyl substitution. Briefly explain your reasoning. (5 points) Rank
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
Does anyone know the answer to these?
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic attack. Most reactive Least reactive butyl acetate 3-methylpentanoyl chloride acetaldehyde acetic propionic anhydride N,N-diphenylethanamide propanone
Help I've tried so many answers Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution. Most reactive to least reactive?: Acetic anhydride, hexyl propanoate, benzamide, benzoyl chloride