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slavikrds
1 month ago
15

In living organisms, C-14 atoms disintegrate at a rate of 15.3 atoms per minute per gram of carbon. A charcoal sample from an ar

chaeological site has a C-14 disintegration rate of 9.16 atoms per minute per gram of carbon. Estimate the age of this sample in years. The half-life of C-14 is 5730 years. (enter only the number of years in standard notation, not the unit years)
Chemistry
1 answer:
lions [2.9K]1 month ago
6 0

Answer:

The result is "4,241.17 years"

Explanation:

The disintegration rate for C-14 atoms is indicated in  15.3 \frac{atoms}{min-g}

The dissolution rate of the sample is given by 9.16 \frac{atoms} {min-gram}

The C-14 proportion within the sample can be determined as per = \frac {9.16}{15.3} \\\\ = 0.5987

With a half-life of 5730 years.

Now, we need to compute the number of half-lives (n) that are applicable:

(\frac{1}{2})^n= A\\\\A= fraction of C-14, which is remaining \\\\(\frac{1}{2})^n= 0.5987 \\\\ n \log 2 = - \log 0.5987\\\\

\therefore \\\\ \Rightarrow n= \frac{0.227}{0.3010} \\\\ = 0.740\\

Thus, the age of the sample is represented as = n \times\ half-life

                                                 = 0.740 \times 5730 \ years \\\\=4241.17 \ years\\\\

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Students dealing with ionic bonds comprehend better how to convey what the model should showcase.

Explanation:

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1 month ago
A certain liquid has a density of 2.67 g/ cm3. what is the mass of 30.5 ml of this liquid? (
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Hello!

density = 2.67 g/cm³

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1 month ago
Calculate the number of grams of carbon dioxide produced from complete combustion of one liter of octane by placing the conversi
Tems11 [2777]

Answer:

15.71g

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The combustion equation that applies to hydrocarbons is

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C8H18 + ( 8 + 18/4 ) O2 = 8CO2 + 9H2O

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From this balanced reaction,

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6 0
1 month ago
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While the original inquiry is incomplete, the comprehensive question is:

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Typically, using chromic acid to visualize spots during the conversion of alcohol to ketone is not feasible. The alcohol (substrate) will convert into its respective ketone due to the presence of chromic acid, causing the spots for the product and the reactant to align horizontally. This alignment complicates differentiation between the spots, making chromic acid unsuitable for this purpose.

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