Answer:
1) After adding 15.0 mL of the HCl solution, the mixture is before the equivalence point on the titration curve.
2) The pH of the solution after adding HCl is 12.6
Explanation:
10.0 mL of 0.25 M NaOH(aq) react with 15.0 mL of 0.10 M HCl(aq). Let's calculate the moles of each reactant.
There is an excess of NaOH so the mixture is before the equivalence point. When HCl completely reacts, we can calculate the moles in excess of NaOH.
NaOH + HCl ⇒ NaCl + H₂O
Initial 2.5 × 10⁻³ 1.5 × 10⁻³ 0 0
Reaction -1.5 × 10⁻³ -1.5 × 10⁻³ 1.5 × 10⁻³ 1.5 × 10⁻³
Final 1.0 × 10⁻³ 0 1.5 × 10⁻³ 1.5 × 10⁻³
The concentration of NaOH is:
![[NaOH]=\frac{1.0 \times 10^{-3} mol }{25.0 \times 10^{-3} L} =0.040M](https://tex.z-dn.net/?f=%5BNaOH%5D%3D%5Cfrac%7B1.0%20%5Ctimes%2010%5E%7B-3%7D%20mol%20%7D%7B25.0%20%5Ctimes%2010%5E%7B-3%7D%20L%7D%20%3D0.040M)
NaOH is a strong base so [OH⁻] = [NaOH].
Finally, we can calculate pOH and pH.
pOH = -log [OH⁻] = -log 0.040 = 1.4
pH = 14 - pOH = 14 - 1.4 = 12.6
C,
takes dead things, makes them into other things
Answer:
He was the first scientist to observe and describe bacteria and protozoa by looking at a drop of water from a pound under a microscope. He also was the one to build the first compound microscope.
Hope this helps :)
The hydrocarbon is used in excess.
<h3><u>Explanation</u>:</h3>
The bromination of an arene is not simple as bromination of an alkane. This is because the carbocation or free radicle formation in benzene is a very energy consuming process. This is why a lewis base like aluminium bromide or ferric bromide is used. The ferric bromide takes in the bromine radicle and forms the brominium cation which helps in the formation of electrophile. Now this electrophile brominium cation attacks the benzene ring and forms a temporary sp3 hybrid carbon intermediate. Then the hydrogen is taken by the FeBr4- forming HBr and regenerating the FeBr3 as well as Aromaticity of the arene species at the same time. Here hydrocarbon is used in excess just to prevent the chances of multiple substitution in the same arene molecule.
