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11 Nov 2019

Consider the four different solutions listed in the table below.

Solution
Number Type of Solution

1 0.15 m fructose

2 0.042 m fructose

3 0.15 m KBr

4 0.030 m KBr

(a) Predict which of these solutions will display the greatest elevation in boiling point.

(b) Predict which of these solutions will display the least elevation in boiling point.

(c) which one of the bolded word makes that statement correct

If the van't Hoff factor for Solution 3 (0.15 m KBr) is determined experimentally, it will be less than/ about equal to/ more than the ideal value. As a result, the measured value of boiling-point elevation will be less than/about equal to/more than the calculated value of boiling-point elevation.

Solution Number	Type of Solution
1	0.15 m fructose
2	0.042 m fructose
3	0.15 m KBr
4	0.030 m KBr

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I need help writing a purpose for a chemistry experiment. I feel I was always do a great job, but my professor always gives me 3 out of 6. Iâm out of ideas. She wants us to summarize the introduction, and summarize what you will do in each section of the experiment and state how this work will support the goal of this experiment being longer than 1/2 a page. She also said not to go into depth on calculations just summarize each section in procedure. Please, please help me right a better purpose for the experiment below. Thanks.

Experiment 5 Analysis of Copper in a Brass Sample

Introduction

A.General

The purpose of this experiment is to determine the percentage of copper present in an unknown brass sample spectrophotometrically using a Spectronic 20. Brass is an alloy consisting of tin, lead, copper, and zinc. The brass sample has already been ground to a fine powder.

A standard curve (graph) will be made for Cu⁺² in which a plot of absorbance (instrument reading from the Spectronic 20) versus molarity of Cu⁺² for various solutions will be made. These standard Cu⁺² will be made by dissolving the appropriate amount of CuSO₄ * 5H₂O is distilled water. The brass samples will be made by dissolving the brass in concentrated HNO₃ to produce Pb⁺², Cu⁺², Zn⁺² is solution along with the finely divided white hydrated tin (IV) oxide solid. After the properly prepared solutions have been filtered to remove the tin (IV) oxide, the absorbance of these solutions will be measured using the Spectronic 20. The molarity of Cu⁺² in these solutions will be obtained from the standard curve. Then the percent copper in the brass sample will be calculated.

B.Method of Analysis

In each of the 5 solutions (3 for determining the standard curve and 2 for the determination of copper in brass) the molarity of Cu⁺² present will be determined spectrophotometrically using the Bausch & Lomb Spectronic 20. The only species in the solution that absorbs at 620 mÂµ (this wavelength corresponds to the visible portion of the electromagnetic waves) in Cu⁺². In this aqueous solution Cu⁺² is really present as the aquo complex [Cu(H₂O)₆]⁺². The other species Pb⁺², Zn⁺², H⁺, NO₃^-, SO₄^-2, and H₂O do not absorb at the 620 mÂµ wavelength of light (and tin is precipitated as hydrated tin (IV) oxide).

In the Spectronic 20, light of wavelength of 620 mÂµ and certain initial intensity, I₀ is allowed to pass through the sample. The wider the sample tube (width = b) and the greater the molarity of Cu⁺², the more absorption will occur causing the intensity of the 620 mÂµ wavelength (I) to be less as it leaves the solution. The following equation describes the process quantitatively: A = log I₀ / I = abM, where A = absorbance (quantity actually measured by the Spectronic 20), M = molarity of the absorbance species (Cu⁺² in this experiment), b = tube diameter, and a = constant which is characteristic of each absorbing species. Since the same tube (a special tube called a cuvette is used for spectrophotometry) is used throughout the experiment, b remains constant. Hence, we can define a new constant, K = ab. Therefore, the above equation becomes: A = KM = K [Cu⁺²]. A plot of A (the absorbance value measured by the use of the Spectronic 20) versus the molarity of Cu⁺² should be a straight line going through the origin (A = 0.000 and M = 0.000).

Three standard Cu⁺² solutions will be made by dissolving a known amount of CuSO₄ * 5H₂O in distilled water. Hence, the molarity of these solutions will be known. Then the absorbance value for each of these three solutions will be measured using the Spectronic 20. A plot of the three absorbance values versus the corresponding Cu⁺² molarities will be done. The best straight line is drawn through these three points and the origin.

With the standard curve, the molarity of Cu⁺² in any Cu⁺² solution can be determined by measuring the absorbance value of the solution (always using the same cuvette and Spectronic 20) and referring to the standard curve to find the molarity of Cu⁺² that corresponds to that absorbance value. Thus, the molarity of Cu⁺² in the brass sample solutions can be obtained from the standard curve after their absorbance values have been measured on the Spectronic 20.

Procedure

Preparation of Brass Sample Solutions

Weigh two brass samples between 0.6 to 0.8 g (to three d.p.). This is done by putting a small clean, dry beaker (100 or 150 mL) on the pan of the balance. Zero the balance. Carefully add the unknown to the beaker until you get a weight somewhere between 0.6 to 0.8 g (Record to 3 d.p.). To each beaker (under the hood) add 12 mL of 8 M nitric acid very slowly. The reaction of 8 M acid with the finely divided brass sample occurs vigorously. The 8 M must be added slowly to prevent splattering of the brass sample out of the container. The reaction is performed in the hood to prevent toxic brown NO₂ gas from entering the lab. After the initial reaction, leave the beaker in the hood but mix occasionally over 30 mins (during this 30 mins the known CuSO₄ * 5H₂O solutions (Part B) can be measured on the Spectronic 20.)

After the brass has reacted with the 8 M nitric acid, wash down the sides of the beaker with some distilled water from a squeeze bottle. Quantitatively, with no spillage transfer the mixture to a clean 50 mL volumetric flask. After solution is poured into the volumetric flask, add more distilled water to the beaker, washing the sides of the walls. Pour this quantitatively into the volumetric flask as mentioned above. Repeat this two more times. Then add enough distilled water until the 50.00 mL mark is reached by the bottom of the meniscus of the solution. Stopper and mix very well by continually shaking the flask in the upright and inverted positions.

The blue solutions must be filtered to remove the tin (IV) oxide or an incorrect high reading will be obtained for the absorbance reading due to the scatter of the light waves. Filter each of the solutions through dry Whatman No. 1 filter paper. (Use 2 pieces to avoid another filtration. Place one piece on the other. Fold in half and then fold in half again. Open it up into a cone and place it into a filter funnel.) Collect the filtrate in clean, dry beakers. If the filtrate is not a clear pale(blue) color, then another filter again with new Whatman filter paper and with clean, dry beakers. One to three filtrations maybe needed, depending on how much tin was present in the brass sample. Now measure the absorbance of these two solutions as described in the section âUse of the Spectronic 20.â Be sure you do these absorbance measurements and the three from part B on the same Spectronic 20.

Preparation of known CuSO₄ * 5H₂O solutions

The three known (standard solutions have already been prepared for you. They are ready for use in their cuvettes by the side of the Spectronic 20 instrument. These three solutions were prepared for you by the stockroom personnel as described in the procedure in the next paragraph. All you need to do is to measure the absorbance of these three prepared standard solutions.

Weigh three 50 mL volumetric flasks (to 3 d.p.). To each of these volumetric flasks add about 1.000, 2.000, and 3.000 grams of CuSO₄ * 5H₂O. Again weigh the volumetric with the CuSO4 * 5H2O (to 3 d.p.). Add 6.0 mL of concentrated nitric acid (measured with a graduated cylinder) and approx. 25 mL of distilled water to each flask. Mix until CuSO₄ * 5H₂O dissolves. Then add distilled water until the bottom of the meniscus of the solution hits the 50.00ML mark. Stop and mix well (as previous section for making the brass solutions). Measure the absorbance of each solution as described in the section âUse of the Spectronic 20.â Be sure you do these absorbance measurements and the three from part A on the same Spectronic 20.

Use of Spectronic 20

How to use the Spectronic 20 and measure the absorbance of each solution is described on another document I will give. Remember wavelength should be set at 620 mÂµ.

Question 11 pts

Which general statement about gases is NOT correct?

The molecules of a pure gas are distributed evenly throughout the container.

Gases are much less dense than liquids or solids

Molecules in a gas mixture can form layers according to their densities

Gases can be compressed, even to the point of liquefaction

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Question 21 pts

Which example is the greatest pressure?

1.00 atm

101 kPa

760 mm Hg (= 760 torr)

All of the above pressures are equal.

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Question 31 pts

Which example is the greatest pressure?

850 mm Hg (= 850 torr)

1.5 atm

All of the above pressures are equal.

96 kPa

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Question 41 pts

Assuming all other variables are held constant, a graph of which of the following will NOT yield a straight line?

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Question 51 pts

A sealed vessel contains 0.250 mol of oxygen gas. Which of the following will result in a decrease in the pressure of the oxygen gas?

increasing the number of moles of oxygen

increasing the temperature of the vessel

increasing the volume of the vessel

adding some helium to the vessel

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Question 61 pts

According to Charlesâs law, which change will cause the pressure of a gas to double? Pressure and amount of gas are constant.

The temperature decreases from 650 K to 325 K.

The temperature of the sample decreases fromï¿½88 Â°C to 44 Â°C.

The temperature of the sample increases fromï¿½22 Â°C to 44 Â°C.

The temperature of the sample increases fromï¿½250 K to 500 K.

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Question 71 pts

Which set of units for P, V, and T can be used for combined gas law calculations?

torr, L, and Kelvins

tm, g/L, and Kelvins

atm, mL, and degrees Celsius

inches of mercury, g/mL, and degrees Celsius

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Question 81 pts

The vapor pressure of a gas is

the atmospheric pressure at which the boiling point is determined.

the pressure at a Kelvin temperature exactly two times the boiling point.

impossible to determine experimentally without knowing the temperature and volume.

the pressure above a gas sample when evaporation and condensation are balanced.

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Question 91 pts

In a chemistry experiment where CO2 is collected over water, the atmospheric pressure is 755 mm. The partial pressure of water at the temperature in the lab is 24.2 mm. What is the pressure of the CO2?

779 mm

731 mm

More information is needed to answer this question

755 mm

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Question 101 pts

Which statement is NOT true according to the kinetic molecular theory of gases?

Molecules undergo elastic collisions

Molecules move in straight-line paths.

Molecules of different gases have differentï¿½kinetic energies at the same temperature

Molecules occupy a negligible volume.

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Question 111 pts

Which statement is NOT true according to the ideal
gas law?

At constant P & T, V must increase when n increases.

At constant V & T, P must decrease when n decreases.

At constant V & n, P must increase when T increases.

At constant P & n, V must decrease when T increases

If you were to over-titrate your calcium solutions in Part B of this lab:a.Would the calculated molarity of EDTA be too high or too low? Explain.

b.Would the calculated molarity of calcium unknown in part C be too high or too low? Explain.

Part B Setup: Complete the following steps, after reading page 6 on how to use volumetric glassware:1.You should have already used a 500 mLvolumetric flaskto prepare an approximately 0.010 M solution of Na2EDTA (Part 1).2.Clean the buret carefully and rinse it two or three times with small amounts (~5mL) of your EDTA solution. Hint; use a clean, dry, labeled beaker to pour solution into the buret. Make sure you rinse through the tip and that no air bubbles are in the tip. Mount the buret on a ring stand using buret clamps. Fill the buret with your EDTA solution nearly to the top mark (to somewhere between the 0 and 5 mL marks for every trialâDO NOT waste time filling the buret to exactly 0.00 mL!). The EDTA is the titrant,the solution added during the titration. Chemistry 161 Lab5Bozlee -Based on S. Critchlow Winter 2018page 4of 11Green River Community College Standardization of the EDTA solution:4.Record the exact reading of the liquid level (bottom of the meniscus) in the buret, recording to the nearest 0.01 mL. This is your initial volume. Note:The burets can be read to a precision of at least +/-0.02 mL. Be sure that all of your readings are precise and consistent.Check with your instructor if you are unclear whether your buret readings are correct.5.In a clean dry beaker, take about 50 mL of standard 0.01000 MCa2+solution; do not take more than this at a time. This is enough to do two trials; if only doing one trial take no more than 30 mL. After proper rinsing, pipet 20.00 mLof this standard Ca2+solution into a 125 mL Erlenmeyer flask. The volumetric pipet tip should NOT be âblown out.â Add about 25 mL of deionized water to the flask.The volume of water is not critical.6.Add a few drops (~6) of indicatorand one full dropperfulof the buffer solutionto the solution in the Erlenmeyer flask.7.Place the stir bar in the flask, place the flask on the stir plate, and set the control for gentle stirring. Or, if you have a good swirling technique with the Erlenmeyer flask, the stir bar and plate is unnecessary. It is essential that the solutions be continually stirred or swirled while titrating.8.What net volume of titrant should be required for the standard trials? You should be able to predict this by calculation!Slowly add your EDTA solution from the buret until the endpoint is reached. The endpointin this titration is the point at which the solution in the Erlenmeyer flask first turns a distinct blue. The color change of the indicatorat the endpoint signals that the equivalence pointhas been reached, where the reactants are in the correct stoichiometric ratio to completely react. As you near the endpoint, add EDTA drop by drop to avoid âovershooting the endpoint.â Record to the nearest 0.01 mL the exact liquid level of EDTA in the buret (your final volume), and calculate the net volume of EDTA used in the titration by subtracting the initial volume from the final volume of EDTA.9.Discard your waste in the appropriate container, using only a very small amount of DI water as the first rinse. Then rinse out your Erlenmeyer flask thoroughlywith several portions of DI water at your sink. Refill the buret (always to between 0 and 5 mL) if you will do another trial. 10.Repeat steps 4-9 two more times, using a fresh aliquot(measured sample) of standard Ca+2solutioneach time. Ideally your replicate titrations should agree within 0.2 mL

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