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Carboxylate salts
Carboxylate salts are less reactive than esters in nucleophilic acyl substitution reactions for two reasons. First, resonance stabilization of carboxylate salts is particularly significant because carboxylates have two identical, significant resonance structures;
Between a proton and electron in a hydrogen atom = 3.16 x 10 47 A 0
4-nitrotolouene ---> LiAlH 4 converts it to 4-aminotoluene ----> Add HNO 2 and it forms -----> diazonium salt ------> add H 3 PO 2 to get Toluene -----> add Br 2 /CCl 4 - 2
Higher fatty acids - Carboxylic acids Stearic, Palmitic, and oleic acids are found in natural fats and oils like glyceryl esters. Higher fatty acids derived their names from
Platinichloride Method for Bases - Chemical Methods Organic bases combine along with chloroplatinic acid, H 2 PtCl 6 to make insoluble platinichlorides, that on ignition, opt
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A Carnot heat engine gets heat at 800 K and rejects the waste heat to the environment at 300 K. The whole work output of the heat engine is used to drive a Carnot refrigerator that
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