Fill in the "Reactions" in the provided Data Table I've already tried to complete most of the table. Need you to check the reactions I have + I'm not sure what the reaction is for the second box (I left it blank)  The procedure is attached and a flow chart  Sample Procedure Observation for Known (Week 1) Chemical Equation(s) Observation for Unknown (Week 2) Conclusion for Unknown (Week 2) Part A Step 1 & 2 & 3 Solution (acidified with HNO3) + 12M HCL (2 drops) + 6M HCL (2 drops) White precipitate: precipitate washed (step 6)                   supernatant saved for Part B Reactions: 1. Ag+ + Cl- → AgCl(s) 2. Hg22+ + 2Cl- → Hg2Cl2(s) 3. Pb2+ + 2Cl- → PbCl2(s)   White precipitate   Pb2+, Hg22+, and Ag+ possible Part A Step 7 & 8 Precipitate + hot H2O (10 drops) Some precipitate dissolves into solution supernatant for step 9 precipitate for step 10 Reaction: 1. Remaining precipitate =     Part A Step 9 Supernatant + 2 drops of 1M K2CrO4 Yellow precipitate Reaction: 1. Pb2+ + CrO42- → PbCrO4­(s)   Yellow precipitate   Pb2+ is present   Part A Step 10 Precipitate from step 8 + 10 drops of 15M NH­3 Gray-Black precipitate formed Reaction: 1. Hg2Cl2 + 2NH3 → Hg + HgNH2Cl(s) + NH4+(aq) + Cl-(aq) Supernatant saved for next step   Gray-black precipitate     Part A Step 10 Supernatant from above + 6M HNO3 until acidic to litmus White precipitate formed Reaction: 1. AgCl + 2NH3 → [Ag(NH3)2+(aq) + Cl- (aq)   White precipitate

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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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Fill in the "Reactions" in the provided Data Table

I've already tried to complete most of the table.

Need you to check the reactions I have + I'm not sure what the reaction is for the second box (I left it blank) 

The procedure is attached and a flow chart 

Sample

Procedure

Observation for Known (Week 1)

Chemical Equation(s)

Observation for Unknown (Week 2)

Conclusion for Unknown (Week 2)

Part A

Step 1 & 2 & 3

Solution (acidified with HNO3)

+ 12M HCL (2 drops)

+ 6M HCL (2 drops)

White precipitate: precipitate washed (step 6)                   supernatant saved for Part B

Reactions:

1. Ag+ + Cl- → AgCl(s)

2. Hg22+ + 2Cl- → Hg2Cl2(s)

3. Pb2+ + 2Cl- → PbCl2(s)

 

White precipitate

 

Pb2+, Hg22+, and Ag+ possible

Part A

Step 7 & 8

Precipitate + hot H2O (10 drops)

Some precipitate dissolves into solution

supernatant for step 9

precipitate for step 10

Reaction:

1.

Remaining precipitate =

 

 

Part A

Step 9

Supernatant + 2 drops of 1M K2CrO4

Yellow precipitate

Reaction:

1. Pb2+ + CrO42- → PbCrO(s)

 

Yellow precipitate

 

Pb2+ is present

 

Part A

Step 10

Precipitate from step 8 + 10 drops of 15M NH­3

Gray-Black precipitate formed

Reaction:

1. Hg2Cl2 + 2NH3 → Hg + HgNH2Cl(s) + NH4+(aq) + Cl-(aq)

Supernatant saved for next step

 

Gray-black precipitate

 

 

Part A

Step 10

Supernatant from above + 6M HNO3 until acidic to litmus

White precipitate formed

Reaction:

1. AgCl + 2NH3 → [Ag(NH3)2+(aq) + Cl- (aq)

 

White precipitate

 

Aqueous solution of cations
HCI(aq)
Aqueous solution of
other cations
AgCI(s), Hg,CL(s), PbCl,(s) (analysis in Part A)
white
(save for Part B)
hot H,0
AgCI(s), Hg,Cl,(s)
Pb2 (aq)
white
colorless
NH,(aq)
K,Cro̟(aq)
Hg(1), H9NH,CI(s)
[Ag(NH,)J(aq)
PbCro,(s)
gray-black
colorless
yellow
HNO,
AgCl(s)
white
Figure 22.2. Flowchart for Part A.
Transcribed Image Text:Aqueous solution of cations HCI(aq) Aqueous solution of other cations AgCI(s), Hg,CL(s), PbCl,(s) (analysis in Part A) white (save for Part B) hot H,0 AgCI(s), Hg,Cl,(s) Pb2 (aq) white colorless NH,(aq) K,Cro̟(aq) Hg(1), H9NH,CI(s) [Ag(NH,)J(aq) PbCro,(s) gray-black colorless yellow HNO, AgCl(s) white Figure 22.2. Flowchart for Part A.
Part A. Separation and Analysis of Metal Cations Ag, Pb?*,
and Hg," (Figure 22.2)
1. PMace 20 dreps of a known saolution or 20 drops of an unknown solucion in a 10 x 75 mm or
13 X L00 mm seM tube. Add 3 drops of 6 M nitric acid. Test the solution with litmus paper
to see if che solution is acidic. If it is sill basic, add 6 M HNO,, dropwise until the solution
is acidic. One of che mon important variables contailling chemical reactions is the pH of the
solution.
2. Nest add 2 drops of concetrated (12 M) hydrochloric acid. HCI. Stir the solution for 3
minutes. (Ie is hard to overstir.) Follow along on your flowchart in Figure 22.2. Yoa are pre-
cipitating metal chlorides. Some precipitates funm alewly and require both time and thorough
mixing. After 5 minutes, allow the precipitate to setle.
3. Now add I drop of 6 M hydrochloric ocid, HCl, solution so determine whether precipication
Is complese. If peccipitation is nor compkee you will observe more forming, In this case, stir
and add more drops of 6 M HCl until no moee procipitate is formed.
4. Cool the test eabe by diorine i inro cold wer. Then cererikr (Labeeatory Methods 1)
the misnure. If che sample a stil aspendal, cenrifge again. If ihis sill does not work. you
may find ik helpful o hear the ample in the waer badh for a few minates, chereby peomotins
formation of largr crysab of solid. which wnd to cenirifuge moe caly
S Carefuly decant (Laboratory Methods G) the vapernatant liquid into another cest tube ana
av. f the solution is aor decanted ckanly and seme peecipitate is presene in the Mpernatant.
cmtrifuging and decanting mut be epested
6 Wash the precipite wich a few drops of distilod water. Washing is done to remove residual
Iiquid left in the tear tube. This quid concaim sample lon that can incerfere with farther tesS
on the wlid. Add the wash liquid, wales, which does not incerfere wih the analysis, and wir
thoroughly to disperse the elid in the wash, Centrifiuar and decare the wash solurion into
the test ube contraining the original vapernatane liquid that you uved. Sar ais sapermataur
liynid far the analynle in Part B (eaniona that did nar precipitate in HCO.
7. Add 10 drops of hot warer so the precipitne, uir, and heat the tet ube in a hoe water bath
(Laboeatory Methods DI) to near beiling Folkow alang on the flowchart in Flgure 22.2 and
see that any lead(II) chloride should dissolve in she hor warer, and mercury() chloride or ilver
chloride should remain aa precipitate. Make sure you recoed any observations on your data
page.
8. Afier hearing, ceniriuge the hot mianure. and decant the hot upermatant liquid inco a tew
test tube. Wash the precipitae with 2-3 deops of hot water, omirifuge, and decant the wash
solution into the test be containing vupernatan liquid Save the precipicane for Hg" and
Ag resing lf PCI, is t compleoedy disolrad and separated from Hg,Cl, ualid, P will
later eacr with the Part A sest for Hg,. This will be purtkulatly confusing if Hg. is not
prese because you will obeain a white, insolahle l6(OHX1 rather chan a gray-black snlid. t
i dacoret o confirne Hg" frew shv ad pyr.
9. Allow the supematant iquid from the peevinas puragraph to cool. Then add a few dropi of 1
M potasium chromate, K,CO, mlution so several drops of the vupematant liquid. A yellow
precipirate of lead chremate, PbCO, indicaes che presence of Po,
10. Te a precipicare of siver chloride, AgCl, ar mercury(I) chloride, He.Cd, (saved from step
8), ald 10 drops of concenirated (15 M) aquous ammonia. NH, A gray-black precipitane
of mercury, and mercury(II) amidochloride, HgNH,ICI, indicates the presence of Hg.".
Cenerifuge the mixnure, and decant the supermatant liquid. To the wupematant liquid, add
6M nicrk acid. HNO solution dropwise until the solucion glves an acidic reaction to blue
litma paper. A white poecipitate of AgCl indkares che peesence of Ag.
Transcribed Image Text:Part A. Separation and Analysis of Metal Cations Ag, Pb?*, and Hg," (Figure 22.2) 1. PMace 20 dreps of a known saolution or 20 drops of an unknown solucion in a 10 x 75 mm or 13 X L00 mm seM tube. Add 3 drops of 6 M nitric acid. Test the solution with litmus paper to see if che solution is acidic. If it is sill basic, add 6 M HNO,, dropwise until the solution is acidic. One of che mon important variables contailling chemical reactions is the pH of the solution. 2. Nest add 2 drops of concetrated (12 M) hydrochloric acid. HCI. Stir the solution for 3 minutes. (Ie is hard to overstir.) Follow along on your flowchart in Figure 22.2. Yoa are pre- cipitating metal chlorides. Some precipitates funm alewly and require both time and thorough mixing. After 5 minutes, allow the precipitate to setle. 3. Now add I drop of 6 M hydrochloric ocid, HCl, solution so determine whether precipication Is complese. If peccipitation is nor compkee you will observe more forming, In this case, stir and add more drops of 6 M HCl until no moee procipitate is formed. 4. Cool the test eabe by diorine i inro cold wer. Then cererikr (Labeeatory Methods 1) the misnure. If che sample a stil aspendal, cenrifge again. If ihis sill does not work. you may find ik helpful o hear the ample in the waer badh for a few minates, chereby peomotins formation of largr crysab of solid. which wnd to cenirifuge moe caly S Carefuly decant (Laboratory Methods G) the vapernatant liquid into another cest tube ana av. f the solution is aor decanted ckanly and seme peecipitate is presene in the Mpernatant. cmtrifuging and decanting mut be epested 6 Wash the precipite wich a few drops of distilod water. Washing is done to remove residual Iiquid left in the tear tube. This quid concaim sample lon that can incerfere with farther tesS on the wlid. Add the wash liquid, wales, which does not incerfere wih the analysis, and wir thoroughly to disperse the elid in the wash, Centrifiuar and decare the wash solurion into the test ube contraining the original vapernatane liquid that you uved. Sar ais sapermataur liynid far the analynle in Part B (eaniona that did nar precipitate in HCO. 7. Add 10 drops of hot warer so the precipitne, uir, and heat the tet ube in a hoe water bath (Laboeatory Methods DI) to near beiling Folkow alang on the flowchart in Flgure 22.2 and see that any lead(II) chloride should dissolve in she hor warer, and mercury() chloride or ilver chloride should remain aa precipitate. Make sure you recoed any observations on your data page. 8. Afier hearing, ceniriuge the hot mianure. and decant the hot upermatant liquid inco a tew test tube. Wash the precipitae with 2-3 deops of hot water, omirifuge, and decant the wash solution into the test be containing vupernatan liquid Save the precipicane for Hg" and Ag resing lf PCI, is t compleoedy disolrad and separated from Hg,Cl, ualid, P will later eacr with the Part A sest for Hg,. This will be purtkulatly confusing if Hg. is not prese because you will obeain a white, insolahle l6(OHX1 rather chan a gray-black snlid. t i dacoret o confirne Hg" frew shv ad pyr. 9. Allow the supematant iquid from the peevinas puragraph to cool. Then add a few dropi of 1 M potasium chromate, K,CO, mlution so several drops of the vupematant liquid. A yellow precipirate of lead chremate, PbCO, indicaes che presence of Po, 10. Te a precipicare of siver chloride, AgCl, ar mercury(I) chloride, He.Cd, (saved from step 8), ald 10 drops of concenirated (15 M) aquous ammonia. NH, A gray-black precipitane of mercury, and mercury(II) amidochloride, HgNH,ICI, indicates the presence of Hg.". Cenerifuge the mixnure, and decant the supermatant liquid. To the wupematant liquid, add 6M nicrk acid. HNO solution dropwise until the solucion glves an acidic reaction to blue litma paper. A white poecipitate of AgCl indkares che peesence of Ag.
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