Answer: The rate constant for the reaction is 
Explanation:
Expression for rate law for first order kinetics is given by:

where,
k = rate constant
t = age of sample = 559 min
a = let initial amount of the reactant = 
a - x = amount left after decay process = 



The rate constant for the reaction is 
When the pressure is increased, the equilibrium will shift to the left to offset the pressure increase. Equilibrium shifting to the left side is favored because the left side has fewer moles of gas than the number of moles of gas on the right-hand side and because it exerts less pressure. Therefore, the answer is there will be a shift toward the reactants.
acid
when a metal hydroxide reacts with acid it forms a salt and water, for example:
lithium hydroxide + hydrochloric acid → lithium chloride (the salt) + water
The ability of sodium sulfate to act as an antidote to barium chloride poisoning is because displaces barium in barium chloride to form sodium chloride and insoluble harmless barium sulfate.
<h3>Why is a solution of sodium sulfate used as an antidote?</h3>
The ability of sodium sulfate to act as an antidote to barium chloride poisoning is because of the reactivity of sodium.
Sodium is a more reactive metal than barium, so it displaces barium in barium chloride to form sodium chloride and insoluble harmless barium sulfate.
The equation of the reaction is given below:
- BaCl2 + Na2SO4 ----> BaSO4 + NaCl
Therefore, the ability of sodium sulfate to act as an antidote to barium chloride poisoning is because displaces barium in barium chloride to form sodium chloride and insoluble harmless barium sulfate.
Learn more about about reactivity of metals at: brainly.com/question/24866635
Answer:
Nucleophilic reaction
and
Explanation:
A nucleophilic reaction is a type of reaction that involves attack of a specie having a negative charge or a lone pair of electrons on a positive center. This negatively charged specie or specie having a lone pair of electrons is called a nucleophile.
An SN2 reaction is a bimolecular, concerted nucleophilic reaction that leads to inversion of configuration at the carbon center. The leaving group is the group that departs from the frontside of the molecule as the nucleophile attacks from the backside.