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Addition of H2 to acetylene gives ethane...

Addition of `H_2` to acetylene gives ethane in présence of palladium but if `BaSO_4` and quinoline or sulphur are also added, the prodụct is ethene. Why?

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.CH=CH+H_2 stackrelPdlongrarrarrow CH_pm=CH_2, stackrelH_2 / pdlongrarrarrow. Acetylene Ethene .CH_3-CH_x. Ethane Mixture of .BaSO_+. and quinoline/sulphur-poison the catalyst. Hence the efficiency of the catalyst decreases and the reaction stops at the first stage of reduction. Hence ethene is obtained.
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Paragraph Carboxylic acids are distinctly acidic because they ionize in water to give hydronium ions: RCOOH+H_(2)O hArr RCOO^(-) +H_(3)O^(+) The acidic strength depends upon the extent of ionizations of the acid and the stability of the anion formed. The acidic strength can also be expressed in terms of dissociation constant K_(a) or pK_(a) which are related as pK_(a)= -log K_(a) . Most unsubstituted carboxylic acids have K_(a) values in the range of 10^(-4) to 10^(-5) (pK_(a) =4-5) . The substitutents have marked effect on the acidic strength of carboxylic acids. Any group that stabilizes the carboxylate ion more than the carboxylic acid group will increase the acidic strength, and the group which destabilizes the carboxylate group more than the carboxylic acid group will decrease the acidic strength. In a similar manner, the electron-releasing groups makes benzoic acid weaker, while the electron-withdrawing groups make benzoic acid stronger. The ortho isomer of every substituted benzoic acid (whether electron releasing or electron withdrawing) is the strongest among the three isomers due to ortho effect. Which of the following is the weakest acid?

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A dark brown solid (X) reacts with NH_3 to form a mild explosive which decompuses to give a violet coloured gas(X)also reacts with H_2 to give an acid (Y). (Y) can also be prepared by heating its salt with H_3 PO_4 .X and Y are

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