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1 answer:
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Answer:
cis-3-hexene and trans-3-hexene
Explanation:
Hydroboration oxidation is a method of preparation of alcohol from alkene.
Hydroboration follows anti-Markovnikoff rule in which alcohol group attached to less substituted carbon. Stereochemistry of the product is always syn that is H and OH attached to the same side of the double bond.
cis-3-hexene and trans-3-hexene undergoes hydroboration to form 3-hexanol.
Answer:
5-chloro-1,3-cyclopentadiene
Explanation:
5-chloro-1,3-cyclopentadiene will react more slowly in an SN1 reaction. ( i.e. No reaction as the product is unstable ) attached is the representation of the rate of reaction of both Halides which shows that 5-chloro-1,3-cyclopentadiene reacts the slowest .
Also During SN1 reaction Carbocation is formed .
Attached below is the solution explanation
