<span>Nucleophilic acyl substitution describe a class of substitution reactions involving nucleophiles and acyl compounds. In this type of reaction, a nucleophile – such as an alcohol, amine, or enolate – displaces the leaving group of an acyl derivative – such as an acid halide, anhydride, or ester. The resulting product is a carbonyl-containing compound in which the nucleophile has taken the place of the leaving group present in the original acyl derivative. Because acyl derivatives react with a wide variety of nucleophiles, and because the product can depend on the particular type of acyl derivative and nucleophile involved, nucleophilic acyl substitution reactions can be used to synthesize a variety of different products.</span>
Answer:
the solubility of the ionic solid decreases
Explanation:
If a salt MX is added to an aqueous solution containing the solute AX, the X^- ion is common to both of the salts. The presence of X^- in the solution will suppress the dissolution of AX compared to the solubility of AX in pure water. This observation is known as common ion effect in chemistry.
The origin of common ion effect is based on Le Chatelier's principle. The addition of a solute will drive the equilibrium position towards the left hand side.
Answer:27,430J/g.K
Explanation:q= mass* specific heat capacity * change in temperature (kelvin)
22*4.184*[(100-25) + 273]
22*4.184*298
27,430J/g.K
So you do 1.5 moles times 44(molar mass of co2) which you get 66 grams