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- Rank the attached compounds in order of increasing reactivity in asubstitution reaction with −CN as nucleophile.Rank the nucleophiles in following group in order of increasing nucleophilicity. H2O, −OH, CH3CO2-Rank the following compounds in order of increasing reactivity in a substitution reaction with −CN as nucleophile.
- Pleas explain how this process occurs. Identify SN1, SN2, E2, E1, nucleophiles and electrophiles.Which compound(s) is (are) best suited for nucleophilic aromatic substitution reactions?Rank the reactivity of the compounds below toward nucleophilic acyl substitution by writing the compounds' letters in the proper blanks in the box below. `NH CI Br CH3 CH3 A В C E rank compounds for acyl substitution reactivity most least reactive reactive
- Which of the following compound is least likely to undergo a nucleophilic substitution reaction?Rank the following esters from most reactive to least reactive in the first slow step of a nucleophilic acyl substitution reaction (formation of the tetrahedral intermediate): Rank the same esters from most reactive to least reactive in the second slow step of a nucleophilic acyl substitution reaction (collapse of the tetrahedral intermediate).Rank the following reactions in order of increasing nucleophile strength: Cl-, H2O, CH3-, H2S, HS-, I-
- Rank the following in increasing order of reactivity towards nucleophilic acyl substitutiona. CH3COCl, CH3COOCH3, CH3CONH2b. CH3COOCH3, CH3COOCH2CCl3, CH3COOCH(CF)3H3C-C O: H ethanal :CN: and the electrophile is cyanide ion In the step you have just written, the nucleophile is slow rate-determining Ö—0—1 H3C-C-C=N; adductWhich of the following could act as a nucleophile? A) HCl B) CH3NH2 C) BF3 D) CH3Br