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Standard addition. Selenium from 0.108 g of Brazil nuts was converted into the fluorescent product in Reaction 18-15, and extracted into 10.0 mL of cyclohexane. Then 2.00 mL of the cyclohexane solution were placed in a cuvet for fluorescence measurement. Standard additions of fluorescent product containingSe/mL are given in the table. Construct a standard addition graph to find the concentration of Se in the 2.00-mL unknown solution. Find the wt%of Se in the nuts and its uncertainty and 95% confidence interval

Short Answer

Expert verified

The interval is3.56±0.068104%3.56±0.22104%

Step by step solution

01

Find equation of intensity:

Is+Xfluorescence intensity from the unknown + standard addition Vtotal volume of (unknown + standard)V0 fluorescence intensity from unknown initial concentration of Unknown initial concentration of standard VSvolume of standard.

Is+xVV0=Ix+Ix[X]i[S]iVsV0

02

Spreadsheet:

03

Graph

The graphIS+xVV0

Versus is,[S]iVsV0

The x-intercept is the concentration of Se. We calculate x-intercept by dividing b / a. So, the concentration of Se is0.03842μg/mL

04

Calculate :

w(Se)=m(Se)m(nuts)Where Mass of Se is,m(Se)=Vγ(Se)m(Se)=10mL0.03842μg/mLm(Se)=0.3842μgw(Se)=0.3842106g0.108gw(Se)=3.56104%

05

Spreadsheet:

06

Calculate the interval:

The standard deviation of x-intercept is calculated by formula:

sy|a|1n+y¯2a2Σxix¯2

n is a number of data, y is a average of y,xiare individual values of x, and is average of x.

xiX¯2

The relative uncertainty in the intercept is:

0.0007320.03842=1.91%

Uncertainty of :

0.01923.56104%=6.84106%3.56(±0.068)104%

95% confidence interval is calculated:

±t. standard deviation

t is a Student's t. We read value from Table 4-4. The degrees of freedom are:

n - 2 = 5 - 2 =3

For 95% confidence level and 3 degrees of freedom, the value is 3.182.

3.1820.068104%=0.22104%3.56(±0.22)104%

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Most popular questions from this chapter

Ammonia can be determined spectrophotometrically by reaction with phenol in the presence of hypochlorite(OCl-)

A 4.37 - mgsample of protein was chemically digested to convert its nitrogen into ammonia and then diluted to 100.0mL. Thenof the solution were placed in a 50 - mLvolumetric flask and treated with 5mLof phenol solution plus 2mLof sodium hypochlorite solution. The sample was diluted to 50.0mLand the absorbance at 625nmwas measured in a 1.00 - cmcuvet after 30min. For reference, a standard solution was prepared from 0.0100g of NH4Cldissolved in 1.00Lof water. Then 10.0mLof this standard were placed in a50 - mL volumetric flask and analyzed in the same manner as the unknown. A reagent blank was prepared by using distilled water in place of unknown.

(a)Calculate the molar absorptivity of the blue product.

(b)Calculate the weight percent of nitrogen in the protein.

What is the difference between fluorescence and phosphorescence?

Nitrite ionNO-2, is a preservative for bacon and other foods, but it is potentially carcinogenic. A spectrophotometric determination ofNO-2makes use of the following reactions

Here is an abbreviated procedure for the

determination:

1. To 50.0ml of unknown solution containing nitrite is added 1.00mL of sulfanilic acid solution.

2. After 10min , 2.00mL of 1 –a minonaphthalene solution and 1.00 mL of buffer are added.

3. After 15 min, the absorbance is read at 520 nm in a 5.00-cm cell.

The following solutions were analyzed:

A. 50.0 mL of food extract known to contain no nitrite (that is, a negligible amount); final absorbance =0.153.

B. 50.0mL of food extract suspected of containing nitrite; final absorbance \(=0.622\).

C. Same as B, but with 10.0μLof7.50×103MNaNO2added to the 50.0-mL sample; final absorbance =0.967.

(a) Calculate the molar absorptivity, of the colored product. Remember that a \(5.00\)-cm cell was used.

(b) How many micrograms ofNO-2were present in 50.0mL of food extract?

Preparing standards for a calibration curve.

(a) How much ferrous ammonium sulfate(FeNH42SO426H2OFM392.15)should be dissolved in a 500mL volumetric flask withto obtain a stock solution with1000μgFe/mL?

(b) When making stock solution (a), you weighed out 3.627 g of reagent. What is the Fe concentration in?

(c) How would you prepare 250mL of standard containing containing ~1,2,3,4,5,6,7,8and10in0.1MH2SO4infrom stock solution (b) using only 5- and 10-mL Class A pipets, only 250mL volumetric flasks, and only two consecutive dilutions of the stock solution? For example, to prepare a solution with ~4μgFe/mL,, you could first dilute 15mL(=10+5mL) of stock solution up to 250 mL mLto get~(1525)(1000μgFFe/mL)=∼60μgFe/mL Then dilute 15mL of the new solution up to 250 mL again to get~(15250)(60μgFe/mL)=∼3.6μgFe/mL

Consider a molecule that can fluoresce from the S1 state and phosphoresce from the T1 state. Which is emitted at longer wavelength, fluorescence or phosphorescence? Make a sketch showing absorption, fluorescence, and phosphorescence on a single spectrum.

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