Answer:
in both nucleophil attach the c and leaving group leave but in acyl nu. subsituation c of carbonyl because of double bond with o have bigger positive charge and is better electrophil so do it faster,also alkyl nu. subsituation can have rearangment if going from sn1 and in sn2 sterichemistry of molecule change , acyl nu. subsituation most of time is better
Answer:
H+(aq) + OH-(aq) → H2O(l)
Explanation:
Step 1: Data given
nitrious acid = HNO3
sodium hydroxide = NaOH
Step 2: The unbalance equation
HNO3(aq) + NaOH(aq) →NaNO3(aq) + H2O(l)
The net ionic equation, for which spectator ions are omitted - remember that spectator ions are those ions located on both sides of the equation - will , after canceling those spectator ions in both side (Ba^2+ and Br-), look like this:
H+(aq) + NO3-(aq) + Na+(aq) + OH-(aq) →Na+(aq) +NO3(aq) + H2O(l)
H+(aq) + OH-(aq) → H2O(l)
The result of Moseley's revisions were that the elements were arranged in atomic number order rather than atomic mass order.