Write balanced equations and draw the structure for any reactions undergone by each alkyl halide with NaI/Acetone:
2-bromobutane, 2-bromo-2-methylpropane, 1-bromobutane, bromocyclohexane, 1-bromoadamantane
and write out mechanism for the reaction 2-bromobutane in NaO/Acetone
Write balanced equations and draw the structure for any reactions undergone by each alkyl halide with NaI/Acetone: 2-bro...
Write balanced equations and draw the structure for any reactions undergone by each alkyl halide with Nal/Acetone: 2-bromobutane, 2-bromo-2-methylpropane, 1- bromobutane, bromocyclohexane, 1-bromoadamantane and write out mechanism for the reaction 2-bromobutane in NaO/Acetone
Write balanced equations and draw the structure for any reactions undergone by each alkyl halide with AgNO3/ethanol 2-bromobutane, 2-bromo-2-methylpropane, 1-bromobutane, bromocyclohexane, 1-bromoadamantane and write out mechanism for the reaction of 2-bromobutane in AgNO3/Ethanol
•Write balanced ean for all rans that occurred with Na Ito • Nal/acetone. ila-bromo butane (Draw all structures for all organic 2) 2-bromo-2 methyl propane Compands) -3) 1-bromo butane 4) bromo cyclohexane 5) 1-bromo adamantane • Write (Draw out mechanism for the ran of 2 - bromobutane in all structures for all organic compounds) Na Il acetone. Ag NOzlethanol •Write balanced earn for all rons that occurred with (Draw all structures for all organic compounds) 12-bromo-2-methylpropane 2) 1-bromo butane 3)...
which alkyl halide reacts fastest with sodium iodide in acetone: 1-bromobutane, 2-bromobutane or 2-bromo-2-methylpropane? explain why
Name Exp. 10 Post-lab Report Organic Chemistry I Nucleophilic Substitution Reactions PART 1.Nal /acetone Alkyl halide Structure 1-bromobutane 1-chlorobutane 2-chlorobutane 2-chloro-2- methylpropane chlorobenzene benzyl chloride
1. Write the general equation for the reaction of an alkyl halide (RX, where R = alkyl group and X = halide) with AgNO3 in ethanol. Indicate which product will precipitate out of solution. 2. Write the general equation for the reaction of an alkyl halide (RX, where R = alkyl group and X = halide) with Nal in acetone. Indicate which product will precipitate out of solution. 3. Draw a complete reaction mechanism using the curved-arrow notation for each...
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...
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
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
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