Answer:
Explanation:
Assume the reaction is the combustion of propane.
Word equation: propane plus oxygen produces carbon dioxide and water
Chemical eqn: C₃H₈(g) + O₂(g) ⟶ CO₂(g) + H₂O(g)
Balanced eqn: C₃H₈(g) + 5O₂(g) ⟶ 3CO₂(g) + 4H₂O(g)
(a) Table of enthalpies of formation of reactants and products
(b)Total enthalpies of reactants and products
ΔᵣH° is negative, so the reaction is exothermic.
3.16 X 10^-11 M is the [OH-] concentration when H3O+ = 1.40 *10^-4 M.
Explanation:
data given:
H30+= 1.40 X 10^-4 M\
Henderson Hasslebalch equation to calculate pH=
pH = -log10(H30+)
putting the values in the equation:
pH = -log 10(1.40 X 10^-4 M)
pH = 3.85
pH + pOH =14
pOH = 14 - 3.85
pOH = 10.15
The OH- concentration from the pOH by the equation:
pOH = -log10[OH-]
10.5= -log10[OH-]
[OH-] = 10^-10.5
[OH-] = 3.16 X 10^-11 is the concentration of OH ions when hydronium ion concentration is 1.40 *10^-4 M.
Answer:
See figure 1
Explanation:
On this case we have a <u>base</u> (methylamine) and an <u>acid</u> (2-methyl propanoic acid). When we have an acid and a base an <u>acid-base reaction </u>will take place, on this specific case we will produce an <u>ammonium carboxylate salt.</u>
Now the question is: <u>¿These compounds can react by a nucleophile acyl substitution reaction?</u> in other words <u>¿These compounds can produce an amide? </u>
Due to the nature of the compounds (base and acid), <u>the nucleophile</u> (methylamine) <u>doesn't have the ability to attack the carbon</u> of the carbonyl group due to his basicity. The methylamine will react with the acid-<u>producing a positive charge</u> on the nitrogen and with this charge, the methylamine <u>loses all his nucleophilicity.</u>
I hope it helps!