The answer is silicon.
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2 answers:
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Answer:
See explanation and images attached
Explanation:
a) In the mechanism for the acid catalysed esterification of propanoic acid using ethanol, we can see that the first step is the protonation of the acid followed by nucleophillic attack of the alcohol. Loss of water and consequent deprotonation regenerates the acid catalyst. We can see the fate of the 18O labelled ethanol in the mechanism shown.
b) In the second mechanism, an unnamed ester is hydrolysed using an acid catalyst. The attack of the acid and subsequent nucleophillic attack of water labelled with 18O leads to the incorporation of this 18O into the product acid as shown in the mechanism attached to this answer.
Answer:
Reagent A: PBr₃
Reagent B: Mg in Et₂O.
Explanation:
Hello,
In this case, your facing a problem in which a carboxylic acid is produced starting by an alcohol. More specifically, cyclopentanol must react with phosphorous tribromide in order to yield bromocyclopentane which is more likely to produce a carboxylic acid, therefore, reagent A is PBr₃.
On the other hand, by means of the production of the specified product, bromocyclopentane must react with carbon dioxide and magnesium in diethyl ether in acidic media to promote the production of the cyclopentanoic acid via the grignard reaction (substitution of the bromine by the carboxyle group), therefore, reagent B is Mg in Et₂O.
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