order of reactivity:
Benzoyl chloride > acetic propanoic anhydride > butanedial > propanone > hexyl propanoate > N,N-diphenyl ethanamide.
Reason: More electron withdrawing nature of group, more will be the reactivity towards attack of nucleophile.
Add curved arrows to the following sets of structures in order to complete the mechanism for...
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.
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
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
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. 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
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
First question: second question: Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution. 3-methylpentanoyl chloride propionamide acetic propionic anhydride isopropyl benzoate In each reaction box, place the best reagent or reactant from the list below. Stoichiometry is omitted.
Complete the electron-pushing mechanism for the following base-promoted hydrolysis of an ester. Add atoms, bonds, nonbonding electron pairs (lone pairs), charges, and curved arrows.
Complete the electron-pushing mechanism for the following base-promoted hydrolysis of an ester. Add atoms, bonds, nonbonding electron pairs (lone pairs), charges, and curved arrows where indicated