Answer would be B. I provided work on an image attached. Message me if u have any other questions on how to do it
Q is unlike K value it describes the reaction that is not at equilibrium.
by considering this reaction:
aA+ bB⇄ cC
and our reaction is:
Br2 + Cl2 ⇄ 2 BrCl
According to Q low:
Q= concentration of products/concentration of reactants
but this equation in the gaseous or aqueous states only.
∴ Q = [BrCl]^2 / [Br2] [Cl2]
and we have [Br2] = 0.00366 m [Cl2]= 0.000672 m [BrCl] = 0.00415 m
by substitution:
= [0.00415]^2 / ( [0.00366] * [0.000672])
∴ Q = 7
Answer:
RbOH → Rb⁺ + OH⁻
As the hydroxide can gives the OH⁻ in water, it is considered as an Arrhenius's base
Explanation:
Arrhenius theory states that a compound is considered a base, if the compound can generate OH⁻ ions in aqueous solution.
Our compound is the RbOH.
When it is put in water, i can dissociate like this:
RbOH → Rb⁺ + OH⁻
As the hydroxide can gives the OH⁻ in water, it is considered as an Arrhenius's base
Answer:
Explanation:
Ketcher 01232019462D 1 1.00000 0.00000 0 5 4 0 0 0 999 V2000 -0.0330 2.2250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0.8330 2.7250 0.0000 C 0 0 0 0 0 0 0 0 0 0 1.6990 2.2250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0.8330 3.7250 0.0000 C 0 0 0 0 0 0 0 0 0 0 1.6990 1.2250 0.0000 C 0 0 0 0 0 0 0 0 0 0 1 2 1 0 0 0 2 3 1 0 0 0 2 4 1 0 0 0 3 5 1 0 0 0 M END
Answer:p-hydroxybenzaldehyde is stronger acid to phenol
para-cyanophenol is stronger acid to meta-cyanophenol
o-fluorophenol is stronger acid to p-fluorophenol.
Explanation:
The PKa tool relative to Ph are used to contrast the pairs.
The pKa of phenol is 10. The pKa of p-hydroxybenzaldehyde is 9.24
The pKa for meta-cyanophenol is 8.61 and the pKa for para-cyanophenol is 7.95.
The pKa value of o-fluorophenol is 8.7, while that of the p-fluorophenol is 9.9. It's obvious that the inductive effect is more dominant at ortho-position, which results in a more acidic nature
The pKa is the pH value at which a chemical species will accept or donate a proton. The lower the pKa, the stronger the acid and the greater the ability to donate a proton in aqueous solution.
