Why is AgNO3/ethanol especially suitable for comparing the relative reactivity of various alkyl halides toward SN1...

Why is AgNO3/ethanol especially suitable for comparing the relative reactivity of various alkyl halides toward SN1 reactions? Comment on the nature of the nucleophile, the nature of the solvent and the ease with which the occurrence of reaction can be detected

Expert Solution

queen_honey_blossom answered 1 year ago

1. Which of the following alkyl halides would not be suitable to make a Wittig reagent...

1. Which of the following alkyl halides would not be suitable to make a Wittig reagent 1-bromo-2-methylpropane 2-bromobutane 2-bromo-2-methylpropane (Bromomethyl)cyclopentane

Give two reasons why tertiary alkyl halides are more likely to eliminate than primary alkyl halides.

Rank in relative order the reactivity of primary, secondary, tertiary, allylic, benzylic and aromatic halides in...

Rank in relative order the reactivity of primary, secondary, tertiary, allylic, benzylic and aromatic halides in sodium/acetone test. Explain the reason for this difference in reactivity.

A. Arrange the organic halides below in order of decreasing experimental reactivity toward iodide ion (NaI...

A. Arrange the organic halides below in order of decreasing experimental reactivity toward iodide ion (NaI in acetone). B. Are there significant differences in the bromides and chlorides? C. What structural change correlates with reactivity in this mechanism (it should be SN2, right?)? Please explain answers! Thank you! halide reagents: 1-bromobutane, 2-bromobutane, 1-chlorobutane, 2-chlorobutane, benzyl chloride, 2-bromo-2-methylpropane, chlorobenzene, bromobenzene, 2-chloro-2-methylpropane

Show how you might synthesize the following compounds, using acetylene and any suitable alkyl halides as...

Show how you might synthesize the following compounds, using acetylene and any suitable alkyl halides as your starting materials. if the compound given cannot be synthesized by this method, explain why. A. hex-1-yne B. hex-1-yne C. hex-3-yne D. 4-methylhex-yne E. 5-methylhex-2-yne F. cyclodecyne

Arrange the following compounds in order of increasing reactivity toward ethanol solvolysis: t-Butyl bromide, t-Butyl iodide,...

Arrange the following compounds in order of increasing reactivity toward ethanol solvolysis: t-Butyl bromide, t-Butyl iodide, isopropyl chloride, isopropyl chloride, and methyl iodide. (Solvolysis is a type of substitution or elimination where the nucleophile is a solvent molecule)

Why is water used for the initial crystallization and ethanol is more suitable to be used...

Why is water used for the initial crystallization and ethanol is more suitable to be used for the recrystallization step of acetylsalicylic acid? (Hint: solubility & temperature)

Which of the following are suitable null hypotheses. If not, explain why. a. Comparing two groups...

Which of the following are suitable null hypotheses. If not, explain why. a. Comparing two groups Consider comparing the average blood pressure of a group of subjects, both before and after they are placed on a low salt diet. In this case, the null hypothesis is that a low salt diet does reduce blood pressure, i.e., that the average blood pressure of the subjects is the same before and after the change in diet. b. Classification. Assume there are two...

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