ADDITION OF HYDROGEN:

Hydrogenation Reaction|| Transfer Hydrogenation ||Birch Reduction|| Wilkinson's Catalyst||1,4 and 1,6 Addition Reaction|| Introduction to EAR|| Dehydrohalogenation Reaction|| (Addition OF HX) X=-F,-Cl,-Br,-I TO alkenes

Questions|Addition Of Sodium Hydrogensulphite (NaHSO3)|Addition Of Alcohols|Reduction|Reactions Due To α-Hydrogen|Summary

Hydrogenation of alkenes and alkynes takes place in presence of certain catalysts. In Sabatier Senderen's reaction, the addition of hydrogen takes place I presence of Raney nickel catalyst. Platininm and palladium can also be used as catalyst and used in finley divided state. Experimentally, it is observed that less crowded alkenes adsorb H_(2) with faster rate. Controlled hydrogenation of alkyne H_(2) with faster rate. Controlled hydrogenation of alkyne in presence of Lindlar's catalyst yields cis product i.e., 'cis' alkene. Thus, in presence of Lindlar's catalyst 'syn' addition takes place. The relative rate of hydrogenation follows the order: Non-terminal alkynes are reduced in presence of Na or Li metal dissolved in liquid ammonia. In this reaction, anti-addition of hydrogen results into the trans-product. Answer the following questions: The relative rate of catalytic hydrogenation of following alkenes is:

Given below are two statements : Statement I : The nucleophilic addition of sodium hydrogen sulphite to an aldehyde or a ketone involves proton transfer to form a stable ion. Statement II : The nucleophilic addition of hydrogen cyanide to an aldehyde or a ketone yields amine as final product. In the light of the above statements, choose the most appropriate answer from the options given below :

Given below are two statements : Statement I : The nucleophilic addition of sodium hydrogen sulphite to an aldehyde or a ketone involves proton transfer to form a stable ion. Statement II : The nucleophilic addition of hydrogen cyanide to an aldehyde or a ketone yields amine as final product. In the light of the above statements, choose the most appropriate answer from the options given below :

Hydrogenation of alkenes and alkynes takes place in presence of certain catalysts. In Sabatier Senderen's reaction, the addition of hydrogen takes place I presence of Raney nickel catalyst. Platininm and palladium can also be used as catalyst and used in finley divided state. Experimentally, it is observed that less crowded alkenes adsorb H_(2) with faster rate. Controlled hydrogenation of alkyne H_(2) with faster rate. Controlled hydrogenation of alkyne in presence of Lindlar's catalyst yields cis product i.e., 'cis' alkene. Thus, in presence of Lindlar's catalyst 'syn' addition takes place. The relative rate of hydrogenation follows the order: Non-terminal alkynes are reduced in presence of Na or Li metal dissolved in liquid ammonia. In this reaction, anti-addition of hydrogen results into the trans-product. H_(3)C-C-=C-CH_(3)+H_(2) overset(Pd//CaCO_(3))underset("Boiling Quinoline")to (A) The product (A) will be:

Hydrogenation of alkenes and alkynes takes place in presence of certain catalysts. In Sabatier Senderen's reaction, the addition of hydrogen takes place I presence of Raney nickel catalyst. Platininm and palladium can also be used as catalyst and used in finley divided state. Experimentally, it is observed that less crowded alkenes adsorb H_(2) with faster rate. Controlled hydrogenation of alkyne H_(2) with faster rate. Controlled hydrogenationof alkyne in presence of Lindlar's catalyst yields cis product i.e., 'cis' alkene. Thus, in presence of Lindlar's catalyst 'syn' addition takes place. The relative rate of hydrogenation follows the order: Non-terminal alkynes are reduced in presence of Na or Li metal dissolved in liquid ammonia. In this reaction, anti-addition of hydrogen results into the trans-product. The product of the following reaction is: