What are strengths and limitations of the AgNO3 test for tertiary alkyl halides?
What are strengths and limitations of the AgNO3 test for tertiary alkyl halides?
Homework Answers
The reaction of alkyl halide with silver nitrate is a SN1 reaction. When silver nitrate reacts with alkyl halide, a white precipitate of silver halide is formed. For this first halide ion shoulde be leave from alkyl halide through breaking carbon-halide bond. This results a carbocation.
When silver nitrate forms a precipitate with tertiary alkyl halide, the resulting carbocation is more stable. So the reaction is fovored.
If this is in the case of primary and secondary alkyl halide, a unstable carbocation are result. Therefore, no reaction occurs with silver nitrate.
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What are strengths and limitations of the AgNO3 test for
tertiary alkyl halides?
Part E Indicate whether each of the alkyl halides is primary, secondary, or tertiary. Drag the...
Part E Indicate whether each of the alkyl halides is primary, secondary, or tertiary. Drag the appropriate items to their respective bins. De asemenea, ang manging CH3CHCH2CH2CH2CI CH3CH2CHCH3 CH, primary secondary tertiary
In detail rationale, What are the strengths and limitations of The Rorschach Test?
In detail rationale, What are the strengths and limitations of The Rorschach Test?
In this experiment we will study the rates of different alkyl halides in different reactions. There...
In this experiment we will study the rates of different alkyl halides in different reactions. There are five alkyl halides selected for this study. Explain the following notation: 1-chlorobutane is a 1° (also called primary) alkyl halide 2-bromobutane is a 2° (secondary) alkyl halide 2-methyl-2-chloropropane is a 3º (tertiary) alkyl halide
3. Draw and classify the following alkyl halides as methyl-, primary (1°), secondary (11°), or tertiary...
3. Draw and classify the following alkyl halides as methyl-, primary (1°), secondary (11°), or tertiary (111°) halide: 10pts -2-chloro-3,3-dimethylhexane; -4-sec-butyl-2-chlorononane; -1-bromo-4-isopropylcyclohexane; -2-chloro-3,3-dimethylhexane; -4-sec-butyl-2-chlorononane; -1-bromo-4-isopropylcyclohexane;
17. Classify the following alkyl halides as primary, secondary, tertiary, or none, as appropriate. 17. Clasifique...
17. Classify the following alkyl halides as primary,
secondary, tertiary, or none, as appropriate.
17. Clasifique los siguientes halogenuros de alquilo como primario, secundario, terciario o ninguno, según corresponda. no-din-an, H, CH–CH, H,C- CH CH, -CH -BrH, -CH CH, HI H,-¢-Br HIV сн. 1
2. Classify the following alkyl halides as primary, secondary, or tertiary. Which one of these options...
2. Classify the following alkyl halides as primary, secondary, or tertiary. Which one of these options would be best suited for a unimolecular nucleophilic substitution reaction? مو لہ کی لہ لا 3. Describe the following reactions in written form, making sure to use the following terms where appropriate: nucleophile, lone pair, loss of leaving group, electron-deficient, and electrophile. . و ». . که ملیہ -- « -
B. Conversion of 3 Alcohols to Alkyl Halides 1. Write the equation for the conversion of...
B. Conversion of 3 Alcohols to Alkyl Halides 1. Write the equation for the conversion of 2-methyl-2-butanol to three alkyl chloride products, one primary, one secondary, and one tertiary. Under the products, write the name of the alkyl chloride. HCI
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...
6. Alkyl halides add to alkenes in the presence of AICI3; yields are the highest when...
6. Alkyl halides add to alkenes in the presence of AICI3; yields are the highest when tertiary halides are used. Predict the outcome of the reaction of tert-pentyl chloride (1-chloro-2.2- dimethylpropane) with propene and specify the mechanistic steps. [6]
1. Compare the reactivity of primary alkyl halides in part 1 (SN2) of this experiment to...
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...
Part E Indicate whether each of the alkyl halides is primary, secondary, or tertiary. Drag the appropriate items to their respective bins. De asemenea, ang manging CH3CHCH2CH2CH2CI CH3CH2CHCH3 CH, primary secondary tertiary
In this experiment we will study the rates of different alkyl halides in different reactions. There are five alkyl halides selected for this study. Explain the following notation: 1-chlorobutane is a 1° (also called primary) alkyl halide 2-bromobutane is a 2° (secondary) alkyl halide 2-methyl-2-chloropropane is a 3º (tertiary) alkyl halide
3. Draw and classify the following alkyl halides as methyl-, primary (1°), secondary (11°), or tertiary (111°) halide: 10pts -2-chloro-3,3-dimethylhexane; -4-sec-butyl-2-chlorononane; -1-bromo-4-isopropylcyclohexane; -2-chloro-3,3-dimethylhexane; -4-sec-butyl-2-chlorononane; -1-bromo-4-isopropylcyclohexane;
17. Classify the following alkyl halides as primary,
secondary, tertiary, or none, as appropriate.
17. Clasifique los siguientes halogenuros de alquilo como primario, secundario, terciario o ninguno, según corresponda. no-din-an, H, CH–CH, H,C- CH CH, -CH -BrH, -CH CH, HI H,-¢-Br HIV сн. 1
2. Classify the following alkyl halides as primary, secondary, or tertiary. Which one of these options would be best suited for a unimolecular nucleophilic substitution reaction? مو لہ کی لہ لا 3. Describe the following reactions in written form, making sure to use the following terms where appropriate: nucleophile, lone pair, loss of leaving group, electron-deficient, and electrophile. . و ». . که ملیہ -- « -
B. Conversion of 3 Alcohols to Alkyl Halides 1. Write the equation for the conversion of 2-methyl-2-butanol to three alkyl chloride products, one primary, one secondary, and one tertiary. Under the products, write the name of the alkyl chloride. HCI
6. Alkyl halides add to alkenes in the presence of AICI3; yields are the highest when tertiary halides are used. Predict the outcome of the reaction of tert-pentyl chloride (1-chloro-2.2- dimethylpropane) with propene and specify the mechanistic steps. [6]
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