Answer:
See explanation
Explanation:
The reaction of a benzyl bromide with a nucleophile may proceed by SN1 or SN2 mechanism depending on the nature of the solvent used.
Since SN1 reaction involves the formation of a carbocation, it usually predominates in the presence of a poor nucleophiles and protic solvents. Hence when methanol is used as solvent and a poor nucleophile is used, SN1 mechanism predominates.
However, when acetone which is an aprotic solvent is used in the presence of a good nucleophile, SN2 reaction mechanism predominates.
<span>This is Pseudoscience. The scientists didn’t study their
experiment, they would have to prove their claim more than once, and they
assumed things before actually studying it. </span>
Answer:
hope the inserted image will help :)
Explanation:
Answer:
I think this is like a game in which you need dice.
Explanation:
To fill out the second page, you need to complete the roll/go-to chart.
