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.
Answer:que es la oms y porque a esta organizacion le preocupan temas como el expuesto
Explanation:
Answer: sharing
Reason: They do this to gain stability. The reason they don’t actually transfer is because the difference in electronegativity values are above a certain value.
