Answer:
Strong acids are assumed 100% dissociated in water- True
As a solution becomes more basic, the pOH of the solution increases- false
The conjugate base of a weak acid is a strong base- true
The Ka equilibrium constant always refers to the reaction of an acid with water to produce the conjugate base of the acid and the hydronium ion- True
As the Kb value for a base increases, base strength increases- true
The weaker the acid, the stronger the conjugate base- true
Explanation:
An acid is regarded as a strong acid if it attains 100% or complete dissociation in water.
The pOH decreases as a solution becomes more basic (as OH^- concentration increases).
Ka refers to the dissociation of an acid HA into H3O^+ and A^-.
The greater the base dissociation constant, the greater the base strength.
The weaker an acid is, the stronger , its conjugate base will be.
Answer:
43.7
Explanation:
mole is equal mass concentration/ moler mass of MgCl²
H₃O⁺ = 
×
OH = 
×
pH = 2.22
pOH = 11.78
<h3>What is pH?</h3>
The term pH, which originally stood for "potential of hydrogen" (or "power of hydrogen"), is used in chemistry to describe how acidic or basic an aqueous solution is. Lower pH values are summarized for acidic solutions (solutions with higher H+ ion concentrations) than for basic or alkaline solutions.
The pH scale is inversely indicates to the concentration of hydrogen ions in the solution and is logarithmic.
⇒pH = -log(
)
Acidic solutions are those with a pH below 7, and basic solutions are those with a pH above 7, at a temperature of 25 °C (77 °F). At this temperature, solutions with a pH of 7 are neutral (e.g. pure water). The pH neutrality relies on temperature, falling below 7 if the temperature rises above 25 °C.
Learn more about pH
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Answer:
Nitrobenzene is too deactivated (by the nitro group) to undergo a Friedel-Crafts alkylation.
Explanation:
The benzene ring in itself does not easily undergo electrophilic substitution reaction. Some groups activate or deactivate the benzene ring towards electrophilic substitution reactions.
-NO2 ia a highly deactivating substituent therefore, Friedel-Crafts alkylation of nitrobenzene does not take place under any conditions.
This reaction scheme is therefore flawed because Nitrobenzene is too deactivated (by the nitro group) to undergo a Friedel-Crafts alkylation.
Answer:
D
Explanation:
Since [pKa = - log Ka]....hence..,the larger the Ka value,the stronger the acid is..so this means that the pKa is vice versa
Saying that the smaller the pKa value..the stronger the acid is.
