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Olenka [21]
4 years ago
14

If a sample of a certain solution is determined to have a [H3O+] concentration of 9.49×10−1 moles/liter, what is its pH? Round o

ff your answer to one decimal place.
Chemistry
1 answer:
almond37 [142]4 years ago
6 0

<u>Answer:</u> The pH of the solution is 1.022

<u>Explanation:</u>

pH is defined as the negative logarithm of hydrogen ion concentration present in a solution.

To calculate the pH of the reaction, we use the equation:

pH=-\log[H^+]

where,

[H^+]=9.49\times 10^{-1}mol/L

Putting values in above equation, we get:

pH=-\log(9.49\times 10^{-1})\\\\pH=1.022

Hence, the pH of the solution is 1.022

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A low-pressure area, or "low", is a region where the atmospheric pressure at sea level is below that of surrounding locations. Low-pressure systems form under areas of wind divergence that occur in upper levels of the troposphere.

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3 years ago
In a thin layer chromatography experiment, a plate of length 9.3 cm was used and a horizontal line was made at 1.45 cm above the
dezoksy [38]

Answer: The R_f value is 0.664

Explanation:

Distance travelled by solvent front = (7.7-1.45)cm = 6.25 cm

Distance travelled by unknown = (5.6-1.45) cm = 4.15 cm

 The retention factor or the R_f value is defined as the ratio of distance traveled by the unknown to the distance traveled by the solvent front.

R_f=\frac{\text {distance travelled by unknown}}{\text {distance travelled by solvent}}

R_f=\frac{4.15}{6.25}=0.664

Thus the R_f value is 0.664

6 0
3 years ago
Why doesn't gravity pull water all the way to the center of the Earth?
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It has to do with force
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3 years ago
List and explain the four most important factors that control the relative reactivity of a carbonyl-containing functional group
ioda

Resonance, leaving group, carbonyl carbon delta+, and steric effect is the most crucial variables that affect the relative reactivity of a functional group containing a carbonyl in an addition or substitution process.

Discussion:

1. Carbonyl Carbon Delta+: The carbonyl group becomes more electrophilic and accelerates nucleophilic assault when the carbonyl carbon delta+ is bigger.

2. Resonance: When the carbonyl is transformed into the tetrahedral adduct, it may be lost. Loss of resonance increases the energy of the transition state for this nucleophilic assault because resonance has the function of stabilizing. Therefore, a carbonyl functional group's resistance to nucleophilic attack increases as resonance in the group increases in importance.

3. Leaving group: Tetrahedral adduct fragmentation is encouraged by a better LG.

4. Steric effects: The nucleophilic attack on carbonyl carbon is delayed when sterically impeded.

Learn more about carbonyl here:

brainly.com/question/21440134

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