RNH2 stands for class of compounds called
If you are referring to a primary amine (RNH2), the shape of the amine part is pyramidal, unless the R group is aromatic (such as phenylamine), in which case the amine part is planar. If you are referring to the Schiff base (RNH2+), the amine component is also planar. If you are referring to the amide ion (NH2-), this has two lone pairs and is a bent molecule just like water.
Potassium carbonate would be better for drying an ether solution containing an acid RCOOH. This is because potassium carbonate can react with the acid to form a salt, reducing the acidity of the solution. However, it may not be effective in drying a base solution containing RNH2 as it could react with the base to form undesirable byproducts.
An Amine is best defined as a derivative of ammonia (NH3) where one or more N-H bonds are replaced by N-C bonds. Primary amines have one N-H bond replaced by a N-c bond, whereas secondary has two N-C bonds with one N-H bond and tertiary has all three N-C bonds making the molecular formula NC3. An amide is a nitrogen bonded to a carbonyl group.
The Nitride ion N3- will be protonated very quickly in an aqueous solution and is therefor not found in solution under ordinary circumstances. If you look at a molecule of water you see that the electrons spend the majority of the time near the oxygen atom, which means the two hydrogen atoms are (for demonstrative reasons) bare protons. A single hydrogen ion would be pulled from the water molecule and would bond with the N3- ion. Under normal circumstances the reaction should go like this: 3H2O + N3- --> 3OH- + NH3 This is an ideal reaction for the nitride ion, however, it is not likely to happen, what will more often than not happen is this: H2O + N3- --> OH- + NH2- THEN H2O + NH2- --> OH-+ NH2- THEN R + NH2- -->RNH2 OVERALL REACTION: R + 2H2O + N3- --> RNH2 + 2OH- This R group could be any other element present in the solution such as a metal impurity that is capable of bonding with an amine or another hydrogen ion. The reason that the nitride will not take both hydrogen's from a water molecule is because it is much more energetically favorable to take a hydrogen from a new water molecule than it is to pull off the second hydrogen to form O2-. This can occur, but will not unless the nitride is in excess, and this simply would never happen under normal circumstances. Edit: Added an overal reaction and fixed the charges on the second phase of the reaction.