Here is the complete question.
Benzalkonium Chloride Solution ------------> 250ml
Make solution such that when 10ml is diluted to a total volume of 1 liter a 1:200 is produced.
Sig: Dilute 10ml to a liter and apply to affected area twice daily
How many milliliters of a 17% benzalkonium chloride stock solution would be needed to prepare a liter of a 1:200 solution of benzalkonium chloride?
(A) 1700 mL
(B) 29.4 mL
(C) 17 mL
(D) 294 mL
Answer:
(B) 29.4 mL
Explanation:
1 L = 1000 mL
1:200 solution implies the
in 200 mL solution.
200 mL of solution = 1g of Benzalkonium chloride
1000 mL will be ![\frac{1000mL}{200mL}=\frac{1g}{xg}](https://tex.z-dn.net/?f=%5Cfrac%7B1000mL%7D%7B200mL%7D%3D%5Cfrac%7B1g%7D%7Bxg%7D)
200mL × 1g = 1000 mL × x(g)
x(g) = ![\frac{200mL*1g}{1000mL}](https://tex.z-dn.net/?f=%5Cfrac%7B200mL%2A1g%7D%7B1000mL%7D)
x(g) = 0.2 g
That is to say, 0.2 g of benzalkonium chloride in 1000mL of diluted solution of 1;200 is also the amount in 10mL of the stock solution to be prepared.
∴ ![\frac{10mL}{250mL}=\frac{0.2g}{y(g)}](https://tex.z-dn.net/?f=%5Cfrac%7B10mL%7D%7B250mL%7D%3D%5Cfrac%7B0.2g%7D%7By%28g%29%7D)
y(g) = ![\frac{250mL*0.2g}{10mL}](https://tex.z-dn.net/?f=%5Cfrac%7B250mL%2A0.2g%7D%7B10mL%7D)
y(g) = 5g of benzalkonium chloride.
Now, at 17%
concentrate contains 17g/100ml:
∴ the number of milliliters of a 17% benzalkonium chloride stock solution that is needed to prepare a liter of a 1:200 solution of benzalkonium chloride will be;
= ![\frac{17g}{5g} = \frac{100mL}{z(mL)}](https://tex.z-dn.net/?f=%5Cfrac%7B17g%7D%7B5g%7D%20%3D%20%5Cfrac%7B100mL%7D%7Bz%28mL%29%7D)
z(mL) = ![\frac{100mL*5g}{17g}](https://tex.z-dn.net/?f=%5Cfrac%7B100mL%2A5g%7D%7B17g%7D)
z(mL) = 29.41176 mL
≅ 29.4 mL
Therefore, there are 29.4 mL of a 17% benzalkonium chloride stock solution that is required to prepare a liter of a 1:200 solution of benzalkonium chloride
A. thermal energy
like when the computer gets hot after running for so long
Answer:
See explanation
Explanation:
For this question, we have to remember the effect of an atom with high <u>electronegativity</u> as "Br". If the "Br" atom is closer to the carboxylic acid group (COOH) we will have an <u>inductive effect</u>. Due to the electronegativity of Br, the electrons of the C-H bond would be to the Br, then this bond would be <u>weaker</u> and the compound will be more acid (because is easier to produce the hydronium ion
).
With this in mind, for A in the last compound, we have <u>2 Br atoms</u> near to the acid carboxylic group, so, we will have a high inductive effect, then the C-H would be weaker and we will have <u>more acidity</u>. Then we will have the compound with only 1 Br atom and finally, the last compound would be the one without Br atoms.
In B, the difference between the molecules is the <u>position</u> of the "Br" atom in the molecule. If the Br atom is closer to the acid group we will have a <u>higher inductive effect</u> and more <u>acidity</u>.
See figure 1
I hope it helps!