Answer:
Both reactions proceeds through nucleophilic acyl substitution reaction
Explanation:
- Both these two reactions proceeds through nucleophilic acyl substitution reaction where phenyl magnesium bromide replaces one ethoxide ion.
- Then another another equivalent of phenyl magnesium bromide give nucleophilic addition reaction with resulting keto group to produce triphenylmethanol
- Full reaction mechanism has been shown below
Kinetic energy maybe or something
Explanation:
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Answer:
2HCL
Explanation:
Both the elements have 2 so when placing the 2 infront ,it'll distribute/ apply to both