Le Chatelier's principle simply explains how equilibria change as you change the conditions of a reaction. If you have a reaction that is at equilibrium lets say (A + 2B <--> C + D) by removing C or D we can drive the reaction forward and products more products. I can provide a more in-depth description if needed.
We can rephrase the statement with a little more specificity in order to understand the answer here.
The mass of the products can never be more than the The mass that is expected.
Answer:
Amino >Methoxy > Acetamido
Explanation:
Bromination is of aromatic ring is an electrophilic substitution reaction. The attached functional group to the benzene ring activates or deactivate the aromatic ring towards electrophilic substitution reaction.
The functional group which donates electron to the benzene ring through inductive effect or resonance effect activates the ring towards electrophilic substitution reaction.
The functional group which withdraws electron to the benzene ring through inductive effect or resonance effect deactivates the ring towards electrophilic substitution reaction.
Among given, methoxy and amino are electron donating group. Amino group are stronger electron donating group than methoxy group. Acetamido group because of presence of carbonyl group becomes electron withdrawing group.
Therefore, decreasing order will be as follows:
Amino >Methoxy > Acetamido
3 H2SO4 + 2 Al(OH)3 → Al2(SO4)3 + 6 H2O
(2.14 g Al(OH)3) / (78.0036 g Al(OH)3/mol) x (3 mol H2SO4 / 2 mol Al(OH)3) / (0.210 mol/L H2SO4) =
0.19596 L = 196 mL H2SO4