Draw the mechanism of these chemicals while mixed with AgNO3
Draw the mechanism of these chemicals while mixed with AgNO3 Br Cl CI Cl Br CI...
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
State whether the reaction mechanism prefers SN1 or SN2. Once sorted, rank in order from most reactive to least reactive. 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
Product structure in AgNO3 EtOH of the following (Note: it should follow an SN2 mechanism). Dont need the entire mechanism just the final product structure please. Thank you. 2-chlorobutane 2-bromobutane 1-chlorobutane 1-bromobutane 2-chloro-2-methyl propane Crotyl chloride Benzyl chloride Bromobenzene Bromocyclohexane Bromocyclopentane
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...
insert the product structure for the reactions AgNO3+ Ethanol (SN1) (Write product structure below) Compound HC 1-Chlorobutane CH HC 2-Chlorobutane CH3 HC 2-Bromobutane Br HC 1-Bromobutane CH3 HC- CI CHE t-butylchloride Benzylchloride Bromobenzene
Draw the reaction equation for the Sodium Iodide/Acetone test (SN2 mechanism) for each of the substances: 1. 1-chlorobutane 2. 2-chlorobutane 3. 2-chloro-2-methylpropane 4. 1-bromobutane 5. 2-bromobutane 6. benzyl chloride 7. bromocyclohexane 8. bromocyclopentane
Explain the reactivities in term of structures (1o, 2o, 3o, and cyclic). Can someone help understand this Table 1: Sodium lodide in Acetone Compound PPT? 2-chlorobutane No precipitate 2-bromobutane Cloudy 1-chlorobutane No precipitate 1-bromobutane Precipitate 2-chloro-2-methylpropane No precipitate bromobenzene No precipitate Table 2: Silver Nitrate in Ethanol Compound PPT? 2-chlorobutane Precipitate 2-bromobutane Precipitate 1-chlorobutane Precipitate 1-bromobutane Precipitate 2-chloro-2-methylpropane Precipitate bromobenzene No precipitate
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
how do I draw mechanism for the reaction of 2-bromo-2-methylpropane with AgNO3 in ethanol? also mechanism for the reaction of 1-bromobutane with NaI in acetone. please use arrows
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...