Name Exp. 10 Post-lab Report Organic Chemistry I Nucleophilic Substitution Reactions PART 1.Nal /acetone Alkyl halide...
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...
(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...
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...
14. Provide the major organic product of the reaction below. Lab Report Nucleophilie Substitution Reactions Section Date Name Part I. Sx/ 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 S2 reactions. 3. Write the complete chemical equations for the Sul and S2 reactions that took place. Use structural formulas for...
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...
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
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...
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
2. Draw the major organic product (bond-line structure) of the following nucleophilic substitution reactions: 1-bromoethane and KOH (in water solvent)???KBr (aq) а. 1-chlorobutane and Nal (in acetone solvent)???+NaCl (s) b.
organic chemistry question kinetic study lab 1) justify why benzyl chloride (PhCH2Cl) reacts faster than 2-Chlorobutane under any of the reaction conditions studied. (Sn2 and Sn1) 2) the compounds 2-bromobutane and 2-clorobutane are secondary alkyl halides. what can be concluded with reactions Sn1 (AgNO3 )and Sn2 (NaI)