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Doing an experiment of nucleophilic substitution reaction of organohalides Sn 1 and Sn 2 , this is the reagent used: Iodoethane ( ethyl iodide )

Doing an experiment of nucleophilic substitution reaction of organohalides Sn1 and Sn2, this is the reagent used:
Iodoethane (ethyl iodide)
1-Chlorobutane (n-butyl chloride)
1-Bromobutane (n-butyl bromide)
2-Chlorobutane (sec-butyl chloride)
2-Bromobutane (sec-butyl bromide)
2-Chloro-2-methylpropane (tert-butyl chloride)
1-Chloro-2-methylpropane (isobutyl chloride)
Bromobenzene
NaI is added for Sn2 reaction (part A)
AgNO3 is added for Sn1 reaction (part B). For this experiment, we are seeing if there is a precipitation formed, and the rate of the precipitation formed.
Based on the data, do the following questions
(a) In cases where heating and/or an extended time was necessary for a precipitate to form, elucidate the reasons behind
these requirements.
(b) If no reaction occurred, explain the absence of precipitate in those instances
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