Answer:
The reaction when the Borane (BH3) is add to an alkene and form an alkylborane is shown below.
Explanation:
The boron of the borane does not have extra electron pairs, in this way the double bond of the alkene attacks the boron and the hydrogen belonging to the borane adheres to the carbon that is more substituted, thus forming an alkyl borane.
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
