Answer:
Explanation:
a ) Benzoic acid is formed . In any alkyl benzene derivative , potassium permanganate reacts to form carboxylic acid . It oxidises side chains to carboxylic acid .
C₆H₅CH₃ + 0 = C₆H₅COOH + H₂O
O is provided by KMnO₄
b ) In this reaction isophthalic acid is formed .
C₆H₄(CH₃)₂ +O = C₆H₄(COOH)₂
c)
4-Propyl-3-t-butyltoluene
In this oxidation , three side chains of ring are 1 ) 1-methyl 2 ) 3- butyl 3 ) 4 propyl .
The methyl and 4 - propyl groups are oxidised to di- carboxylic acid and 3 butyl group remains intact ( unoxidised )
Answer:
pH =3.8
Explanation:
Lets call the monoprotic weak acid HA, the dissociation equilibria in water will be:
HA + H₂O ⇄ H₃O⁺ + A⁻ with Ka = [ H₃O⁺] x [A⁻]/ [HA]
The pH is the negative log of the H₃O⁺ concentration, we know the equilibrium constant, Ka and the original acid concentration. So we will need to find the [H₃O⁺] to solve this question.
In order to do that lets set up the ICE table helper which accounts for the species at equilibrium:
HA H₃O⁺ A⁻
Initial, M 0.40 0 0
Change , M -x +x +x
Equilibrium, M 0.40 - x x x
Lets express these concentrations in terms of the equilibrium constant:
Ka = x² / (0.40 - x )
Now the equilibrium constant is so small ( very little dissociation of HA ) that is safe to approximate 0.40 - x to 0.40,
7.3 x 10⁻⁶ = x² / 0.40 ⇒ x = √( 7.3 x 10⁻⁶ x 0.40 ) = 1.71 x 10⁻³
[H₃O⁺] = 1.71 x 10⁻³
Indeed 1.71 x 10⁻³ is small compared to 0.40 (0.4 %). To be a good approximation our value should be less or equal to 5 %.
pH = - log ( 1.71 x 10⁻³ ) = 3.8
Note: when the aprroximation is greater than 5 % we will need to solve the resulting quadratic equation.
Molar mass NaCl = 58.5 g/mol
C = 158.0 g/L
Molarity = C / molar mass
M = 158.0 / 58.5
M = 2.7000 M
hope this helps!
I believe it is the fourth choice because the producer would use sunlight to make food, then the next choice fhat has anything to do with the producer is [D]. if i’m wrong i’m sorry but I believe that would be the write anwser.
