bromomethane with excess ammonia b)chloroethane with ammonia (1:1 ratio) c)bromomethane with aminoethane (1:1) I don’t understand why it’s (1:1ratio) I always thought it was 1:2 ratio can someone give me the equation for b and c pls
bromomethane with excess ammonia b)chloroethane with ammonia (1:1 ratio) c)bromomethane with aminoethane (1:1) I don’t understand why it’s (1:1ratio) I always thought it was 1:2 ratio can someone give me the equation for b and c pls
im pretty sure in this case 1:1 ratio will simply mean there is equal amounts of both reactants
I don’t understand why it’s (1:1ratio) I always thought it was 1:2 ratio can someone give me the equation for b and c pls
An excess of the haloalkane will lead to the formation of secondary (and then tertiary) amines. If you know/understand the mechanism, you will see that, just like the reactant, the amine product still has a lone pair on the N. In fact the product is a better nucleophile than the initial reactant.