There are:
3.41 moles of C
4.54 moles of H
3.40 moles of O.
Why?
To solve the problem, the first thing that we need to do is to write the chemical formula of the ascorbic acid.
Now, we know that there are 100 grams of the compound, so, the masses of each element will represent the percent in the compound.
We have that:
To know the percent of each element, we need to to the following:
So, we know that for the 100 grams of the compound, there are:
40.92 grams of C
4.58 grams of H
54.49 grams of O
We know the molecular masses of each element:
Now, to calculate the number of moles of each element, we need to divide the mass of each element by the molecular mass of each element:
Hence, we have that there are 3.41 moles of C, 4.54 moles of H, and 3.40 moles of O.
Have a nice day!
Answer:
remaining still during the night.
Explanation:
Answer:125.0964g
Explanation:
Density = mass/volume
Density = 2.7 gcm-3
Volume=2.7*1.2*14.3=46.332
Mass=?
Mass= density* volume
= 2.7× 46.332=125.0964g
Answer:
1.5 × 10² mL
Explanation:
Step 1: Given data
- Initial pressure of the gas (P₁): 1.9 atm
- Initial volume of the gas (V₁): 80 mL
- Final pressure of the gas (P₂): 1.0 atm (standard pressure)
- Final volume of the gas (V₂): ?
Step 2: Calculate the final volume of the gas
For an ideal gas, we can calculate the final volume of the gas using Boyle's law.
P₁ × V₁ = P₂ × V₂
V₂ = P₁ × V₁/P₂
V₂ = 1.9 atm × 80 mL/1.0 atm
V₂ = 1.5 × 10² mL
Since the pressure decreased, the volume of the gas increased.
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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