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emmasim [6.3K]
3 years ago
14

A pure sample contains only nitrogen and oxygen atoms. If the sample is 30.4% nitrogen, by weight, what is the empirical formula

of the molecule? 1. N2O3 2. NO2 3. N2O 4. N2O5 5. NO
Chemistry
1 answer:
andrew-mc [135]3 years ago
8 0

Answer: 2. NO_2

Explanation:

Empirical formula is the simplest chemical formula which depicts the whole number of atoms of each element present in the compound.

a) If percentage are given then we are taking total mass is 100 grams.

So, the mass of each element is equal to the percentage given.

Mass of N = 30.4 g

Mass of O= 69.6 g

Step 1 : convert given masses into moles

Moles of N=\frac{\text{ given mass of N}}{\text{ molar mass of N}}= \frac{30.4g}{14g/mole}=2.2moles

Moles of O=\frac{\text{ given mass of O}}{\text{ molar mass of O}}= \frac{69.6g}{16g/mole}=4.4moles

Step 2 : For the mole ratio, divide each value of moles by the smallest number of moles calculated.

For N = \frac{2.2}{2.2}=1

For O =\frac{4.4}{2.2}=2

The ratio of N: O = 1; 2

Hence the empirical formula is NO_2

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Determine the number of valence electrons for the following: [kr] 5s2 4d6
wlad13 [49]

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3 years ago
Suppose a student started with 142.0 mg of trans-cinnamic acid, 412 mg of pyridinium tribromide, and 2.30 mL of glacial acetic a
nirvana33 [79]

Answer: Theoretical Yield = 0.2952 g

               Percentage Yield = 75.3%

Explanation:

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pyridium tribromide moles = (412mg/1000) / 319.82= 1.288*10⁻³ mol

  • n-trans-cinnamic acid is the limiting reactant

The molar ratio according to the equation mentioned is equals to 1:1

The brominated product moles is also = 9.584*10⁻⁴ mol

Theoretical yield = (9.584*10⁻⁴ mol) * (Mr of brominated product)

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Percentage Yield is : Actual Yield / Theoretical Yield = 0.2223/0.2952

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4 0
3 years ago
Which isomer of 1-bromo-4-tert-butylcyclohexane reacts faster when refluxed with potassium tert-butoxide?
grigory [225]

Answer:

See explanation.

Explanation:

Since potassium tert-butoxide is a strong bulky base, we expect that an elimination reaction predominates.

This reaction is expected to occur by E2 mechanism. The cis isomer of  1-bromo-4-tert-butylcyclohexane is known to react faster by E2 mechanism because it fulfills the anticoplanar arrangement required for for E2 mechanism, where the leaving group and adjacent proton must be anti to each other and in the same plane. The trans isomer can not fulfill this requirement.

7 0
2 years ago
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