It's not so easy for me guys!
I know this is a cakewalk for all geniuses out here!
1 mole each of Bromo-Derivative (A) and NH3 react to give 1 mole of an organic compound (B). B reacts with Methyl Iodide (CH3I) to give (C). Both B & C react with Nitrous acid to give D & E respy. D is oxidised and subsequent decarboxilation of the product gives 2-Methoxy-2Methyl Propane. Identify A to E.
-
UP 0 DOWN 0 1 4
4 Answers
B is the amino derivative...diazotization of it gives D which is the alcohol, oxidation of which gives us a carboxylic acid. But how will we find out where the carboxyl group was located in the product after decarboxylation?
RBr+NH3→RNH2 TO react with a HNO2 we should have an alcohol SO
the compund A is
C6H5Br+NH3→C6H5NH2HNO2→C6H5N2Cl CH3Ithis further reacts to give 2-Methoxy-2Methyl Propane on decarboxyaltion after it is oxidised to Benzoic acid