How would you describe the main difference between direct and back titration? I'm struggling to be concise in my response 
For a direct titration, solutions are slowly added together until an endpoint is reached, using a precisely measured amount of primary standard. In back titration, the solution is neutralised instantaneously by adding as excess of the standard. This is done so accuracy can be preserved when trying to analyse solutions like ammonia, i.e. volatile compounds. If you a direct titration was used instead, the process would be inaccurate because as the aliquot is slowly delivered, the ammonia evaporates. Instead, using a back titration, all of the ammonia is reacted instantly and another titration is then used to determine the amount of excess standard solution.
*I'm sure someone could be more detailed
*I myself have a few questions.
1. In pure water when heated, the pH of the resulting solution will decrease as hydronium concentration increases. Nevertheless, the solution itself is neutral because hydroxide and hydronium are at equal concentrations, which seems somewhat contradictory because the pH indicates an acidic solution. So my question is, are there any other cases where the pH decreases/increases but the solution is still neutral? Thanks.
2. When doing questions using acidity constants, in what cases do we make the assumption (let the acid be HA) that [H
+] = [A
-], or more simply, the concentration of products on the left hand side are equal? In what cases can we make this assumption and in what cases should we not (I came across a VCAA question where people did but it was incorrect - the specific question has slipped my mind)?
Just to make sure you understand my question:

Let [H
+] = [A
-]

When do and don't we make this assumption?
Thank you!