Calculate the ratio by using Henderson-Hasselbalch equation:
pH = pKa + log [neutral form] / Protonated form
3.05 = 2.21 + log [neutral form] / [Protonated form]
3.05 - 2.21 = log [neutral form] / [Protonated form]
0.84 = log [neutral form] / [Protonated form]
[neutral form] / [protonated form] = anti log 0.84 = 6.91
Answer:

Explanation:
Hello there!
In this case, for these problems about collecting a gas over water, we must keep in mind that once the gas has been collected, the total pressure of the system is given by the atmospheric pressure, in this case 1.01 atm. Next, since we also have water in the mixture, we can write the following equation:

Thus, by solving for the pressure of nitrogen and using consistent units, we obtain:

Answer:
0.26 moles
Explanation:
Number of moles = mass/molar mass
Mass of SiO2 = 15.5g
Molar mass of SiO2 = 60.08g/mol
Number of moles = 15.5g/60.08g/mol
=0.257
= 0.26 moles
Answer is: gamma emission or gamma decay.
<span>During gamma emission the nucleus emits radiation without changing its composition, if for example have nucleus with six protons and six neutrons (carbon atom) and after gamma decay there is nucleus with six protons and six neutrons.
</span>Gamma rays are the
electromagnetic waves with the shortest wavelengths (1 pm), highest
frequencies (300 EHz) and highest energy (1,24 MeV).
Answer:
The alkyl halide is secondary
The nucleophile is a poor nucleophile
The solvent is a protic solvent
The product is racemic
Explanation:
The reaction is shown in the image attached.
Alkyl halides undergo nucleophilic substitution by two mechanisms; SN1 and SN2. The particular mechanism that applies depends on;
I) structure of the alkyl halide
ii) nature of the nucleophile
iii) nature of the solvent
Looking at the reaction under review, we can see from the structure that the alkyl halide is a secondary alkyl halide. A secondary alkyl halide may undergo substitution via SN1 or SN2 mechanism depending on the conditions of the reaction.
If the nucleophile is poor, and the solvent is protic, SN1 mechanism is favoured over SN2 mechanism. Since CH3CH2OH is a poor nucleophile and ethanol is a protic solvent, we expect the reaction to proceed via SN1 mechanism leading to the formation of a racemic product.
The organic product is also shown in the second image attached.