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can question A2 part a and b be answered and labeled please.
information has been provided....
can all parts of question A be answered and labeled please. there is no data for...
can all parts of question A be answered and labeled please.
there is no data for precipitation of Nal in acetone.
NUCLEOPHILIC SUBSTITUTION A. Structural Effects on Sa1 and Sa2 Reactivity A1. In the following table, record the results of your group's experiments with the five alkyl halides and the two reagents, sodium iodide in acetone and alcoholic silver nitrate. Note the elapsed time required for turbidity to appear and for a precipitate to form. If you heated any of...
can question A parts A4 (a and b) A5 and A6 be answered neatly and labled....
can question A parts A4 (a and b) A5 and A6 be answered neatly
and labled. with specifics in A5 and A6
Dale Tepot sub Partners NUCLEOPHILIC SUBSTITUTION A. Structural Effects on Sn1 and Sn2 Reactivity A1. In the following table, record the results of your group's experiments with the five alkyl halides and the two reagents, sodium iodide in acetone and alcoholic silver nitrate. Note the elapsed time required for turbidity to appear and for a precipitate to form....
(1) What mechanism do you believe will be favored with Nal in acetone? What order of...
(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...
For the Reactions that formed precipitates, what are the drawn out reaction equations with stereochemistry if...
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...
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...
Read the experiment and briefly describe what you would predict to be your result if you...
Read the experiment and briefly describe what you would predict
to be your result if you were to perform this experiment and
why.
Part A: Determination of Factors Affecting the Relative Rates of Sy2 Reactions All test tubes must be dry. Effect of Structure of the Alkyl Halide Measure 2 mL of 15% sodium iodide in acetone into each of three clean, dry 10-cm test tubes. Add 2 drops of 1-bromobutane (butyl bromide) to the first test tube; add 2...
can question B of B2 and B3 be answered please. information has also been provided B....
can
question B of B2 and B3 be answered please.
information has also been provided
B. Effect of Solvent on SN1 Reactivity B1. In 1. In the following table, record the time in seconds required for the pink color to disappear in each solvent mixture. Compositon (solvent:water) Reaction time in seconds Methanol Ethanol Acetone 6:175 non reachre 2:405 1.1 mL:0.9 mL (55:45) 1.2 mL:0.8 mL (60:40) 1.3 mL:0.7 mL (65:35) 1.4 mL:0.6 mL (70:30) 7:32 5 08 s 6:49 5:475...
Relative ranking (#1 - #7) Reason for ranking 1-chlorobutane 1-chloro-2-butene 2-chlorobutane 1-bromobutane 2-chloro-2-methylpropane bromobenzene benzyl chloride...
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...
Reactivity of Alkyl Halides a. Which test was overall faster? Give a rationale for why that...
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...
2) Predict the order of reactivity (1=least, 4=most) of primary, secondary, tertiary, and aryl halides toward...
2) Predict the order of reactivity (1=least, 4=most) of
primary, secondary, tertiary, and aryl halides toward nucleophilic
displacement by an SN1 reaction mechanism. Explain
3) Give a detailed summary of the chemistry in both reactions
SN2 and SN1 in details please for both reactions. include any
general statements about the experiments.
LAB)o Organic Chemistry I Lab CHEM 3512 Nueleophilic Substitution Reactions: Sl vs S2 To review Sul, S2, El and E2 reactions and mechanisms and compare and contrast the effect...
can all parts of question A be answered and labeled please.
there is no data for precipitation of Nal in acetone.
NUCLEOPHILIC SUBSTITUTION A. Structural Effects on Sa1 and Sa2 Reactivity A1. In the following table, record the results of your group's experiments with the five alkyl halides and the two reagents, sodium iodide in acetone and alcoholic silver nitrate. Note the elapsed time required for turbidity to appear and for a precipitate to form. If you heated any of...
can question A parts A4 (a and b) A5 and A6 be answered neatly
and labled. with specifics in A5 and A6
Dale Tepot sub Partners NUCLEOPHILIC SUBSTITUTION A. Structural Effects on Sn1 and Sn2 Reactivity A1. In the following table, record the results of your group's experiments with the five alkyl halides and the two reagents, sodium iodide in acetone and alcoholic silver nitrate. Note the elapsed time required for turbidity to appear and for a precipitate to form....
(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...
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...
Read the experiment and briefly describe what you would predict
to be your result if you were to perform this experiment and
why.
Part A: Determination of Factors Affecting the Relative Rates of Sy2 Reactions All test tubes must be dry. Effect of Structure of the Alkyl Halide Measure 2 mL of 15% sodium iodide in acetone into each of three clean, dry 10-cm test tubes. Add 2 drops of 1-bromobutane (butyl bromide) to the first test tube; add 2...
can
question B of B2 and B3 be answered please.
information has also been provided
B. Effect of Solvent on SN1 Reactivity B1. In 1. In the following table, record the time in seconds required for the pink color to disappear in each solvent mixture. Compositon (solvent:water) Reaction time in seconds Methanol Ethanol Acetone 6:175 non reachre 2:405 1.1 mL:0.9 mL (55:45) 1.2 mL:0.8 mL (60:40) 1.3 mL:0.7 mL (65:35) 1.4 mL:0.6 mL (70:30) 7:32 5 08 s 6:49 5:475...
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...
2) Predict the order of reactivity (1=least, 4=most) of
primary, secondary, tertiary, and aryl halides toward nucleophilic
displacement by an SN1 reaction mechanism. Explain
3) Give a detailed summary of the chemistry in both reactions
SN2 and SN1 in details please for both reactions. include any
general statements about the experiments.
LAB)o Organic Chemistry I Lab CHEM 3512 Nueleophilic Substitution Reactions: Sl vs S2 To review Sul, S2, El and E2 reactions and mechanisms and compare and contrast the effect...
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