Answer:
No net change in reaction occurs in this nucleophilic acyl subtitution reaction
Explanation:
Sodium ethoxide in ethanol gives nucleophilic acyl substitution reaction with ethyl-2-methylpropanoate.
Here ethoxide group replaces an ethoxide group from ester through addition-ellimination pathway.
So, ultimately, the product of this reaction is identical with reactant i.e. ethyl-2-methylpropanoate is reproduced.
Hence one might observe no change during reaction as product and reactant of this reaction are same.
Mechanistic pathway has been shown below.
Answer:
a.
b. K = 192.9
c. Products are favored.
Explanation:
Hello!
a. In this case, according to the unbalanced chemical reaction we need to balance HCl as shown below:
In order to reach 2 hydrogen and chlorine atoms at both sides.
b. Here, given the concentrations at equilibrium and the following equilibrium expression, we have:
Therefore, we plug in the data to obtain:
c. Finally, we infer that since K>>1 the forward reaction towards products is favored.
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