Rank reactivity of Sn2 reactions with sodium iodine and explain why. 1-chlorobutane, bromocyclobutane, 1-bromo-3-phenylpropane, benzylbromide.
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Rank reactivity of Sn2 reactions with sodium iodine and explain why. 1-chlorobutane, bromocyclobutane, 1-bromo-3-phenylpropane, benzylbromide.
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- Rank the reactivity of the following compounds according to the SN2 reaction? Please explain why a) Methyl chloride b) Methyl iodide c) isopropyl chlorideRank the primary, secondary, tertiary, and aryl halides in terms of reactivity with the nucleophile. Which type of halide react faster by an SN2 reaction? Explain1. In both SN1 and SN2 tests, why should 2-chlorobutane react more slowly than 2-bromobutane?2. Why is benzyl chloride reactive in SN1? In SN2?3. Why is bromobenzene unreactive in both tests?
- Rank the alkyl halides in the following marine natural product in order of increasing reactivity in the SN2 reaction.After E2 elimination, will the following molecule contain deuterium? Why or why not?what structure show the transition state for the rate determining step in the sn1 reaction with this picture?