Relative ranking (#1 - #7) Reason for ranking 1-chlorobutane 1-chloro-2-butene 2-chlorobutane 1-bromobutane 2-chloro-2-methylpropane bromobenzene benzyl chloride...
(1) What mechanism do you believe will be favored with Nal in acetone? What order of reactivity do you predict will be observed when each of the alkyl halides in Figure 1 is reacted with Nal in acetone? Complete the below table; list the relative ranking of the reactivity of the alkyl halides and your reason for placing that alkyl halide at that ranking. Write your prediction of the mechanism and the order of reactivity with Nal in acetone as...
-Compare rates of S2 and SN1 product formation for 5 halides (1-chlorobutane, 1- bromobutane, 2-bromobutane, 2-chloro-2-methylpropane, and chlorobenzene) -Arrange 5 compounds in order of decreasing reactivity toward (a) Nal in acetone, and (b) AgNO3 in ethanol reagents. [Use structural formula for halides]
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...
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?
Halides tert-Butyl chloride 2-Chlorobutane 1-Chlorobutane 1-Bromobutane Bromobenzene Benzyl Chloride Crotyl Chloride Sy Read Lab Report Nucleophilie Substitution Reactions Section Date Name Part I. Sxl and S2 reactivity of different halides 1. Rank the seven halides from the most reactive to the least reactive in their Snl reactions. 2. Rank the seven halides from the most reactive to the least reactive in their SN2 reactions. 3. Write the complete chemical equations for the Syl and SN2 reactions that took place. Use...
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...
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...
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...
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
1. Compare the reactivity of primary alkyl halides in part 1 (SN2) of this experiment to the reactivity of primary alkyl halides today. What conclusions, if any, can you make about the reactivity of these molecules under these different conditions? Use specific data to make your point. 2. Compare the reactivity of secondary alkyl halides in part 1 (SN2) of this experiment to the reactivity of secondary alkyl halides today. What conclusions, if any, can you make about the reactivity...