complete the following table. Compound: Structure: 1°, 2° or 3° RX Predict reactivity (SN1, SN2, both,...
For each compound listed below, predict the dominant mechanism for each reactant (SN1 and/or SN2). The two test reagent mixtures you will be using are sodium iodide in acetone and silver nitrate in ethanol.Note: a compound may not react at all or react under both mechanisms. If both mechanisms are possible, one is usually dominant. Indicate that where applicable. Reactant KI/acetone AgNO3/ethanol 1 bromobenzene 2 bromocyclopentane 3 bromocyclohexane 4 2-bromobutane 5 2-chlorobutane 6 1-chloropropan-2-one 7 1-chlorobutane 8 2-chloro-2-methylpropane 9 1-chloromethylbenzene
For each compound listed below, predict the dominant mechanism for each reactant (SN1 and/or SN2). The test reagent mixture you will be using is silver nitrate (AgNO3) in ethanol. Note: a compound may not react at all or react under both mechanisms. If both mechanisms are possible, one is usually dominant. Indicate that where applicable. 1. bromobenzene 2. bromocylopentane 3. bromocyclohexane 4. 2-bromobutane 5. 2-chlorobutane 6. 1-chloroporpan2-one 7. 1-chlorobutane 8. 2-chloro-2-mehtylpropane 9. 1-chloromethylbenzene
Predict if the given compounds below undergo SN2 or SN1 in presence of NaI / acetone and AgNO3 / ethanol medium. (1-bromobutane, 1-chlorobutane, 2-bromobutane, 2-chlorobutane, 2-chloro-2methylpropane, 2-bromo-2-methylpropane)
Nucleophilic Substitution Reactions Lab (SN1 and SN2 reaction mechanisms) Below are my lab results for SN1 and SN2 reactions. This first column of the chart gives the ten starting material halides used in this experiment. The second column gives the reaction time for SN1 mechanisms with silver nitratate in ethanol solution. The third column gives the reaction time for SN2 mechanisms with sodium iodide. In theory, primary alkyl halides are expected to react faster in SN2 mechanisms, and tertiary alkyl...
Relative ranking (#1 - #7) Reason for ranking 1-chlorobutane 1-chloro-2-butene 2-chlorobutane 1-bromobutane 2-chloro-2-methylpropane bromobenzene benzyl chloride (2) What mechanism do you believe will be favored with AgNO3 in ethanol? What order of reactivity do you predict will be observed when each of the alkyl halides in Figure 1is reacted with AgNOs in ethanol? Complete a similar table as in question #1 for these reaction conditions. Write your prediction of the mechanism and the order of reactivity with AGNO3 in ethanol...
Arrange the alkyl halides in order of reactivity (from most to least reactive) under both SN1 (silver nitrate/ethanol) and SN2 (sodium iodide/acetone) conditions: 1-bromobutane, 2-bromobutane, bromocyclohexane, 2-bromo-2-methylpropane, 1-bromoadamantane, benzyl bromide, and bromobrmzene.
Rank the compounds from most reactive to least reactive under conditions of both SN1 and SN2. Experiment CI Br 1-chlorobutane 1-bromobutane 1-chloro-2-methylpropane B ta Br 2-bromobutane 2-chloro-2-methylpropane 1-chloro-2-butene 2-chlorobutane
Please HELP!! Table 1: Alkyl Halides in NaI Substrate Time for Precipitate to Form Heated? Temp (℃) Time (min) Heat Relative Ranking (#1-#6) Predicted Relative Ranking (#1-#6) Bromobenzene No reaction Yes 44 10 6 6 2-Chlorobutane No reaction Yes 44 10 5 4 1-Chlorobutane 13 min Yes 44 8 4 3 Benzyl Chloride 2min 30 sec No --- --- 2 1 1-Chloro-2-butene 1 second No --- --- 1 5 1-Bromobutane 5 min No --- --- 3 2 1. Why did...
Experiment F. Nucleophilic Substitution Reactions. Pre -Lab Report 2. SPECIAL INSTRUCTIONS: a. Work in groups of 2-3 students. Each group will complete and turn in one report for grade. You will not complete the lab report in your lab notebook using the usual format. Instead, the entire report is provided in the procedures section of these lab materials. You will complete the report by providing the missing information. Report is due at the end of the lab period. b. While...
please fill in the table or answer all rows and columns. thanks. Leaving Group Degree of Substitution Steric Hinderance Stability of Carbocation Name 1-chlorobutane 1-bromobutane v v 2 2-chlorbutane Reactivity Tables (complete the following to hand-in for the experiment) 1-chloro-2-butene "crotyl chloride" 1-chloro-2-methylpropane X 2-chloro-2-methylpropane LL bromobenzene 1-chloroadamantane benzyl chloride