Explain the observed reactivity rate of the following alkyl halides in an S№1 reaction. -CI slowest rate anti-aromatic least stable + non-aromatic -CI CN CN fastest rate Propose the product of the following reaction (hint: this is a two step-reaction. Reaction one is an electrocyclic ring opening and step 2 is a cycloaddition reaction). Be sure to include stereochem in your answer. A O -CI aromatic most stable

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Explain the observed reactivity rate of the following alkyl halides in an SN1 reaction.
-CI
slowest
rate
anti-aromatic
least stable
answer.
+
non-aromatic
CI
CN
Propose the product of the following reaction (hint: this is a two step-reaction. Reaction one is an
electrocyclic ring opening and step 2 is a cycloaddition reaction). Be sure to include stereochem in your
CN
fastest
rate
A
CI
aromatic
most stable
Transcribed Image Text:Explain the observed reactivity rate of the following alkyl halides in an SN1 reaction. -CI slowest rate anti-aromatic least stable answer. + non-aromatic CI CN Propose the product of the following reaction (hint: this is a two step-reaction. Reaction one is an electrocyclic ring opening and step 2 is a cycloaddition reaction). Be sure to include stereochem in your CN fastest rate A CI aromatic most stable
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