Missing question: volume of <span>solution on the left is 10 mL.
V</span>₁(solution) = 10 Ml.
c₁(solution) = 0.2 M.<span>
V</span>₂(solution)
= ?.<span>
c</span>₂(solution)
= 0.04 M.<span>
c</span>₁ -
original concentration of the solution, before it gets diluted.<span>
c</span>₂
- final concentration of the solution, after dilution.<span>
V</span>₁
- <span>volume to
be diluted.
V</span>₂ - <span>final volume after
dilution.
c</span>₁ · V₁ = c₂ · V₂<span>.
</span>10 mL · 0.2 M = 0.04 M · V₂.
V₂(solution) = 10 mL · 0.2 M ÷ 0.04 M.
V₂(solution) = 50 mL.<span>
</span>
Answer:
p-fluoronitrobenzene and sodium phenoxide is more appropriate
Explanation:
An ipso substitution is required to form p-nitrophenyl phenyl ether.
For this ipso substitution, an alkoxide anion needs to attack as a nucleophile at the carbon atom attached to fluorine atom and thereby substitute that F atom.
p-nitrophenoxide is an weak nucleophile as compared to phenoxide due to presence of electron withdrawing resonating effect of nitro group at para position.
p-fluoronitrobenzene is a good choice for nucleophilic attack by alkoxide anion as compared to fluorobenzene due to higher positive charge density at carbon atom directly attached to F atom. Higher positive charge density arises due to presence of electron withdrawing resonating effect og nitro group at para position.
So, p-fluoronitrobenzene and sodium phenoxide is more appropriate
<span>CH4 + 4 Cl2 → CCl4 + 4 HCl
(4.00 mol CH4) x (1/1) x (0.70) = 2.80 mol CCl4
(4.00 mol CH4) x (4/1) x (0.70) = 11.2 mol HCl
CCl4 + 2 HF → CCl2F2 + 2 HCl
(2.80 mol CCl4) x (2/1) x (0.70) = 3.92 mol HCl
11.2 mol + 3.92 mol = 15.1 mol HCl from both steps</span>
Before the development of electrophoresis to separate macromolecules, high-speed centrifugation was used to isolate DNA.
A laboratory procedure called electrophoresis is used to divide DNA, RNA, or protein molecules according to their size and electrical charge. The molecules are moved by an electric current through a gel or other matrix. The technology of electrophoresis is crucial for the separation and examination of nucleic acids. At the lab bench, cloned DNA fragments are frequently isolated and worked with using nucleic acid electrophoresis.
High-speed centrifugation employs centrifugal force to separate particles with various densities or masses suspended in a liquid. High-speed rotation of the solution inside the tube causes each particle's angular momentum to experience centrifugal forces inversely proportionate to its mass.
To know more about electrophoresis refer to: brainly.com/question/28709201
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B, the opposing forces are the same, thus, the ball doesn't move back or forward.
