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2 answers:
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Answer:
See explanation and image attached
Explanation:
This reaction is known as mercuric ion catalyzed hydration of alkynes.
The first step in the reaction is attack of the mercuric ion on the carbon-carbon triple bond, a bridged intermediate is formed. This bridged intermediate is attacked by water molecule to give an organomercury enol. This undergoes keto-enol tautomerism, proton transfer to the keto group yields an oxonium ion, loss of the mercuric ion now gives equilibrium keto and enol forms of the compound. The keto form is favoured over the enol form.
Answer:
0.159 \%
Explanation:
The acid will dissociate according to the reaction shown below:-
Given that, pH=3.8
The concentration of can be determined from the expression fo pH as:-
pH = - log
3.8 = - log
=
The initial concentration of RCOOH was 0.10 M, then the percent dissociation was- calculated as shown below:-