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Gnoma [55]
3 years ago
11

Calculate the Zn conc. of Zn/Zn++ // Cl/Cl- 0.1M Emf=2.21v

Chemistry
1 answer:
Leto [7]3 years ago
5 0

Answer:

Option a. = 0.01 M

Explanation:

To do this, we need to gather the data:

E = 2.21 V

[Cl⁻] = 0.1 M

And the Redox reaction taking place is the following:

Zn(s) + Cl₂(g) <-------> Zn²⁺(aq) + 2Cl⁻(aq)       Q = [Zn] [Cl]²

E° Cl⁻/Cl₂ = 1.36 V

E° Zn/Zn²⁺ = -0.76 V

According to this, the expression to use will be the Nernst equation, and we can assume we are working at 25 °C, therefore, the Nernst equation will be:

E = E° - (0.059/n) logQ

E = E° - (0.059/n) ln([Cl⁻]² * [Zn²⁺])   (1)

From there, we can solve for Zn later.

First, we need to write the semi equation of oxidation and reduction, and get the standard potential of the cell:

Zn(s) --------> Zn²⁺(aq) + 2e⁻       E₁° = 0.76 V

Cl₂(g) + 2e⁻ -----------> 2Cl⁻(aq)   E₂° = 1.36 V

---------------------------------------------------------------

Zn(s) + Cl₂(g) -------> Zn²⁺(aq) + 2Cl⁻(aq)    E° = 0.76 + 1.36 = 2.12 V

Now, let's replace in (1) and then, solve for [Zn]:

2.21 = 2.12 - (0.059/2) log ([0.1]² * [Zn])

2.21 - 2.12 = -0.0295 log (0.01[Zn])

- 0.09 / 0.0295 = log (0.01[Zn])

-3.0508 = log (0.01[Zn])

10^(-3.0508) = 0.01[Zn]

8.8961x10⁻⁴ = 0.01[Zn]

[Zn²⁺] = 0.08896 M

This value can be rounded to 0.1 M. so the correct option will be option A.

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Monosaccharides are colorless crystalline solids that are very soluble in water. Moat have a swwet taste. D-Fructose is the sweetest monosaccharide.

In the open chain form, monosaaccharides have a carbonuyl group in one of their chains. If the carbonyl group is in the form of an aldehyde group, the monosaccharide is an aldose; if the carbonyl group is in the form of a ketone group, the monosaccharide is known as a ketose. glucose is an aldose while fructose is a ketose.

In D-glucose, there is an aldehyde functional group, and the carbonyl group is at carbon-1 when looking at the Fischer projection.

In D-fructose, there is a ketone functional group, and the carbonyl group is at carbon-2 when looking at the Fischer projection.

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18. Suggest an explanation for the observations that ethanol, C2H5OH, is completely miscible with water and that ethanethiol, C2
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Answer:

              Ethanol is completely miscible due to <u><em>presence</em></u> of Hydrogen bonding.

              Ethanethiol is partially miscible due to <u><em>absence</em></u> of Hydrogen Bonding.

Explanation:

                     The miscibility of liquids depend upon the intermolecular interactions between the two liquids. The stronger the intermolecular interactions the more miscible will be the liquids.

Among the two given examples, Ethanol is more miscible in water because it exhibits hydrogen bonding which is considered the strongest intermolecular interaction. Hydrogen bonding occurs when the hydrogen atom is bonded to more electronegative atoms like Fluorine, Oxygen and Nitrogen. In this way the hydrogen atom gets partial positive charge and the electronegative atom gets partial negative charge. Hence, these partial charges results in attracting the opposite charges on other surrounding atoms.

While, in case of Ethanethiol the hydrogen atom is not bonded to any high electronegative atom hence, there will be no hydrogen bonding and therefore, there will be less interactions between the neighbour atoms.

6 0
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If you tried forming an ionic bond between sodium and aluminum, would it work? Why? (please help! this is for a friend)
sineoko [7]

Answer:

The answer to your question is No

Explanation:

Ionic bonding is a kind of bonding that involves the attraction between oppositely charged ions. That means that one element must have a positive charge and the other a negative charge.

Also, the difference in electronegativity of both elements must be higher than 1.7.

Both Sodium and Aluminum are positively charged then an ionic bond is not possible to be formed.

Difference of electronegativity = 1.61 (Al) - 0.93(Na)

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To form an ionic bond the difference of electronegativity must be higher than 1.7.

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