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 |
Product structure in AgNO3 EtOH of the following (Note: it should follow an SN2 mechanism). Dont...
Product Structure in NaI, acetone 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
2-chlorobutane 2-bromobutane 1-chlorobutane 1-bromobutane 2-chloro-2-methyl-propane Allyl chloride Benzyl Chloride Bromobenzene Bromocyclohexane Bromocyclopentane 1. Which substrates should be "very reactive" in SN2 reactions? 2. Which substrates should be "very reactive" in SN1 reactions?
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
Nucleophilic substitutions, mainly just need the arrangements, and the drawn out reaction equations CHEM 220L Laboratory Manual (S.A. Cummings & J.K. Mahoney) CHEM 220L Data Sheet: Nucleophilic Substitutions (SN1 and SN2) (6 points) Part 1. Enter the results of each test into the table below: Alkyl Halides 10, 2 or 3? SN2 (Nal/acetone) 1-chlorobutane 1-bromobutane 2-chlorobutane 2-bromobutane bromocyclohexane 2-chloro-2-methylpropane (t-butyl chloride) Crotyl chloride Benzyl chloride (a-chlorotoluene) Arrange the alkyl halides in order of reactivity (from most to least reactive) with...
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 the Reactions that formed precipitates, what are the drawn out reaction equations with stereochemistry if applicable? Part 1. Enter the results of each test into the table below: 1°, 2° or 3°? Alkyl Halides 1-chlorobutane Sn2 (Nal/acetone) Precipitate formed 1-bromobutane Precipitate formed 2-chlorobutane No precipitate formed 2-bromobutane No precipitate formed bromocyclohexane No precipitate formed 2-chloro-2-methylpropane (t-butyl chloride) No precipitate formed Crotyl chloride No precipitate formed Benzyl chloride (a-chlorotoluene) No precipitate formed Arrange the alkyl halides in order of reactivity...
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
Reactivity of Alkyl Halides a. Which test was overall faster? Give a rationale for why that test is faster. Use one of the substrates to help you explain, drawing an energy diagram might help as well. b.For the AgNO3 test: Which substrate was fastest and which was slowest. Why? Draw a mechanism and energy diagram to help you explain these results. Data Table Test Tube # Reaction Time NaI test Reaction Time AgNo3 test 1 2-chlorobutane 00:03.25 No reaction 2...
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
complete the following table. Compound: Structure: 1°, 2° or 3° RX Predict reactivity (SN1, SN2, both, neither?) 1 2 3 4 5 6 1-chlorobutane 1-chloro,2-methylpropane 2-chlorobutane 2-chloro, 2-methylpropane bromobenzene benzyl bromide