Student Worksheet Organic Chemistry Practice: "Carbohydrate" [PDF]

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STUDENT WORKSHEET ORGANIC CHEMISTRY PRACTICE "CARBOHYDRATE"



Name



: Era Melania



Class



: PKU 2018



Reg. Number



: 18030194085



Chemistry Department Faculty of Mathematics and Natural Science Surabaya State University 2020



Phase 1: Orientation Task 1 a. Equipments which is needed No. Equipments/Materials



Spesification



Function



1.



20 pieces



To react a small



Test tube and rack



amount



of



substances 2.



Pipette



20 pieces



Help to move chemical solution



from



one container to another



on



a



small scale 3.



Measuring flask



2 pieces



To measure a volume



of



liquid substances 4.



Beaker glass



1 piece of 250 Use mL



as



container



1 piece of 600 heat mL



a to



chemical



substances



or



react a larger quantities



of



substances 5.



Spirtus burner



1 piece



To



heat



chemical substances 6.



Tripod/Three-legged



1 piece



To



hold



the



gauze



mats



during



the



heating process 7.



Gauze mats



1 piece



As



a base in



heating process 8.



Wood clamp



1 piece



To hold a hot equipment



9.



2% of glucose



22 drops



As carbohydrate sample



10.



Sucrose



1 mL



As carbohydrate sample



11.



Starch



3 mL



As carbohydrate sample



12.



Lactose



17 drops



As carbohydrate sample



13.



Watery ammonia (in Tollens Sufficienly



To



form



test)



Ag(NH3)2OH complex ion



14.



HCl 3M (in sucrose and 3 mL



As catalys



starch hydrolysis)



b. Reagents that needed No



1.



Experiment tittle/ subtittle Molish Test



Reagent Used Molish reagent



Function of Reagent To test the presence of carbohydrate compound in sample



Reaction  Sucrose HO HO OH



O



CH2OH



O



H



O



H2O, H+



O



HO



OH



OH



Kalor



OH H



Concenrated H2SO4



To avoid and form hydrolysis or break down disaccharide molecules into



HO



+



H



OH OH



CH2OH



H



OH



OH



H



H



CH2OH



OH OH



Sukrosa



Step 1



Glukosa



OH



O



H



Fruktosa



monosaccharides and polysaccharides into disaccharides



H2O, H+



+2 + 3H2O



+2



→ Kompleks berwarna ungu  Glucose H2O, H+



+2 + 3H2O



+2







Kompleks berwarna ungu  Amylum Step 1: Hydrolisis amylum to glucose



+



Step 2:



n



H2O, H+



+2 + 3H2O



+2







Kompleks berwarna ungu 2.



Seliwanoff Test



Seliwanoff reagent



To distinguish between alldose and ketose sugar



 Amylum



 Glucose



 Lactose



3.



Barfoed Test



Barfoed reagent



To differentiate monosaccharides and disaccharides from the samples



 Amylum CH2OH



CH2OH H



O H H H OH



H



H



OH



O H H OH



H



H



OH



O



O



*O



+ 2Cu2+ + 2H2O n



amilum



 Glucose



CH2OH



CH2OH



O H



H



O



H2 O



H



OH



H



C H + 2Cu2+ + 2H O 2



OH OH



OH



OH



OH



OH



Glukosa



CH2OH



COO-



OH



+ Cu2O Endapan merah bata



OH OH



 Lactose OH



CH2OH



CH2OH O



O



O



OH



+ 2Cu2+ + 2H2O



OH OH OH



OH



Laktosa



4.



Tollens Test



Tollens reagent



 Sucrose



To differentiate reduction sugar and non-reduction sugar



HO HO OH



O O



O



OH



HO



HO



OH



fructose



glucose OH



sucrose



CH2OH



+



[Ag(NH3)2]



OH CO2-



OH



+ Ag



OH OH



 Amylum



+ Ag(NH3)2OH (aq) ↛ (aq)



 Lactose



Ag(NH3)2+ OH-



(aq)  Glucose



(aq)



+ Ag (s) silver mirror NaOH solution



To form a brown



2 AgNO3 (aq) + 2 NaOH (aq) →



silver precipitate.



Ag2O (s) + 2 NaNO3 (aq) + H2O(l) (brown precipitate)



NH4OH solution



To dissolve the silver oxide precipitate by forming a complex compound or oxidizing the



Ag2O (s) + 2 NH4OH (aq) → 2Ag(NH3)2OH (aq)



5.



Fehling Test



Fehling reagent



Ag2O compound To test the presence of reducing sugars in the sample



 Fructose



+ (aq) +



Cu2+ →



(aq) + Cu2O(s) (brick red)  Lactose



(aq) + 2Cu2+ →



+ Cu2O(s) (Brick red)  Glucose



6.



Sucrose hydrolysis



HCl solution



To break down sucrose into glucose and fructose



H+, OH-



+



Benedict reagent



To test for sucrose with a brick red precipitate







Glucose



(aq) + Cu2+ (aq) →



+ (aq) + Cu2O (s) 



Fructose



(aq) + Cu2+ →



(aq) + Cu2O (s) Seliwanof reagent



To test for ketosa groups



3H2O, H+



7.



Hidrolisis pati



Iodine



To identify hydrolyzed starch or not + n I2 →



n + 2 H2O (l) tidak terhidrolisis



+ I2 Terhidrolisis Benedict reagent



To test for sucrose with a brick red precipitate



+ Cu2+ (aq) →



(aq) + Cu2O (s) + 3H2O (l)



Phase 2: Conceptualization Task 2 1. Molisch Test a. Purpose and Formulation of the Problem/question Purpose Identify carbohydrate functional groups in the sample Formulation of the Problem/question Does the sucrose sample contain carbohydrates? Does the glucose sample contain carbohydrates? Does the starch sample contain carbohydrates? b. Hypothesis Sucrose, glucose and starch samples contain carbohydrates 2. Seliwanoff Test a. Purpose and Formulation of the Problem/question Purpose To prove the ketose in compund by using seliwanoff reagent Formulation of the Problem/question How the positive result that shown from seliwanoff test? b. Hypothesis In this test the positive result is in succrose and fructose as the sample that mixed with seliwanoff reagent then heated. It will produce red orange solution that identify the presence of ketose in monosaccharide type in carbohidrate 3. Barfoed Test a. Purpose and Formulation of the Problem/question



Purpose To know the presence of reducing monosaccharides and disaccharide by using barfoed test Formulation of the Problem/question How is the positive indication of barfoed test? b. Hypothesis  Foodstuffs which containing monosaccharides will produce brick red precipitate after heated for 2 minutes  Foodstuffs which containing disaccharides will produce brick red precipitate after being heated for 10 minutes 4. Tollens Test a. Purpose and Formulation of the Problem/question Purpose To recognize compound belonging to carbohydrates through tollens test Formulation of the Problem/question How the changes that occur in carbohydrates taht contain aldehyde and ketone groups when reacted with tollens reagents? b. Hypothesis Carbohydrates that contain aldehyde groups when reacted with tollens reagents will form silver mirror, whereas carbohydrates with the ketones groups do not react 5. Fehling Test a. Purpose and Formulation of the Problem/question Purpose: To identify the presence of reducing sugars in the sample Formulation of the Problem/question: 1. What is the definition of reducing sugar? 2. What is the example of reducing sugar? 3. What is the properties of reducing sugar? b. Hypothesis



The solution that contain a reducing sugar will form a brick red precipitate 6. Hydrolysis of Sucrose a. Purpose and Formulation of the Problem/question Purpose: To hydrolysis sucrose molecule become maltose and glucose that will test with benedict and seliwanoff Formulation of the Problem/question What is the reaction that occur in the hydrolysis of sucrose? b. Hypothesis 1. The presence of reducing sugar if tested with benedict reagent will produce brick red precipitate 2. The presence of ketosa groups if tested with seliwanoff reagent will produce red or orange solution 7. Hydrolysis of Pati a. Purpose and Formulation of the Problem/question Purpose 1. Hydrolyze polysaccharides 2. Testing the results of the polysaccharide hydrolysis use iodine and benedict test. Formulation of the Problem/question 1. How to do hydrolysis of polysaccharides? 2. How to test the results of the polysaccharide hydrolysis use iodine and benedict test? b. Hypothesis 1. Polysaccharide which has been hydrolyzed is tested with iodine then no reaction will occur 2. Polysaccharide which has been hydrolyzed is tested with benedict will form a brick red precipitate



Phase 3: Investigation Task 3 1. Molisch Test Variables:  Control variable: 2 drops of Molisch reagents 7-8 drops of H2SO4 concentrated  Manipulation variable: The types of carbohydrate (sucrose, glucose, amylum)  Response variable: The result of Molisch test of sucrose, glucose, amylum Procedure: 2,5 drops of sucrose



2,5 drops of glucose



2,5 drops of starch



1. Added 5 drops of molish reagent 2. Added 10 drops of concentrated sulfuric acid until forms a separate layer from the initial layer



If there is carbohydrate formed a red ring then turns dark purple



3. Leave for 2 minutes 4. Added 5 ml of water



Purple Formed



2. Seliwanoff Test



Variables:  Controlled Variable: 5 drops of seliwanof reagent, shake and heated the mixture on a water bath  Manipulation Variable: sampel test (lactose, glucose, amylum)  Response Variable: time needed to color changes Procedure 1. Test tube 1 5 drops of lactose 1. Added 5 drops of seliwanoff reagent 2. Shake and heated the mixture on a water bath 3. Note the time needed to colour changes Result 2. Test tube 2 5 drops of glucose 1. Added 5 drops of seliwanoff reagent 2. Shake and heated the mixture on a water bath 3. Note the time needed to colour changes Result 3. Test tube 3 5 drops of amylum 1. Added 5 drops of seliwanoff reagent 2. Shake and heated the mixture on a water bath 3. Note the time needed to colour changes Result



3. Barfoed Test Variables:  Control Variable: 5 mL of barfoed reagent 5 drops of sample Heated the mixture on a water bath  Manipulation Variable: sampel test (lactose, glucose, amylum)  Response Variable: There is red brick precipitate Procedure Test Tube 1



Test Tube 2



Test Tube 3



5 mL of Barfoed reagent



5 mL of Barfoed reagent



5 mL of Barfoed reagent



- Added 5 ml of amylum - Heated in a water bath - Wait for 2 minutes



- Added 5 ml of glucose - Heated in a water bath - Wait for 2 minutes



- Added 5 ml of lactose - Heated in a water bath - Wait for 2 minutes



- Observed changes that occur



- Observed changes that occur



- Observed changes that occur



Result



Result



- Wait for 10 minutes



- Wait for 10 minutes



- Observed changes that occur



- Observed changes that occur



Result



4. Tollens Test Variables:



Result



Result - Wait for 10 minutes - Observed changes that occur Result



a. Controlled variable: 5 drops of tollens reagent. b. Manipulation Variables: Various of carbohydrate (sucrose, lactose, amylum, glucose, and fructose). c. Response



variable: Tollens test results for each type of (sucrose,



lactose, amylum, glucose, and fructose). Procedure Making of Tollens Test 1 mL of AgNO3 Solution 1. Put into a test tube 2. 1 mL of NaOH solution is added 3. Mixed Tollens Reagent Tollens Test



2-5 drops of starch



2-5 drops of sucrose



2-5 drops of lactose



2-5 drops of glucose



1. Putted into each test tube 2. Added 5 drops of Tollens reagent 3. Added aqueous ammonia solution drop by drop until all precipitate has dissolved 4. Heated the mixture if no silver mirror is formed



Formed silver mirror 5. Fehling Test Variables:  Control variable: Number of drops.  Response variable: Color change.  Manipulation variable: Sugar solution (sucrose and glucose) Procedure



Making Reagent Fehling Fehling A 1 mL



1. Add fehling B 1 mL Fehling reagent



Test Tube I 2 drops of sucrose



Test Tube II Test Tube III Test Tube IV Test Tube V 2 drops of lactose



2 drops of amylum



2 drops of glucose



1. Add 2 drops of fehling reagent 2. Shake it and heat it Red precipitate



6. Hydrolysis of Sucrose Variables: a. Controlled variable: • 0.5 mL of sucrose b. Manipulation Variable: • Added 1 mL HCl • Added 1 mL of water • Heated and cooled at room temperature • Left at room temperature • Added 1.5 mL NaOH • Types of reagents c. Response variable: sucrose test results from each tube Procedure 0,5 mL sucrose - Dissolved in water Sucrose solution



2 drops of fructose



1 mL Sucrose solution (1) - Added 1 mL HCl 3 M - Boiled in water bath - Cooled at room temperature



- Added 1,5 mL sucrose solution Test tube 1A



Test tube 1B



- Added 5 mL Benedict’s reagen



- Added 2 mL Seliwanof’s reagen



- Boiled in water bath for 5 minutes



- Boiled in water bath for 5 minutes



Result



Result



1 mL Sucrose solution (2) - Added 1 mL water



- Boiled in water bath - Cooled at room temperature - Added 1,5 mL sucrose solution Test tube 1A



Test tube 1B



- Added 5 mL Benedict’s reagen



- Added 2 mL Seliwanof’s reagen



- Boiled in water bath for 5 minutes



- Boiled in water bath for 5 minutes



Result



Result



1 mL Sucrose solution (3) - Added 1 mL water - Cooled at room temperature - Added 1,5 mL water - Divided into 2 test tube equally



Test tube 1A



Test tube 1B



- Added 5 mL Benedict’s reagen



- Added 2 mL Seliwanof’s reagen



- Boiled in water bath for 5 minutes



- Boiled in water bath for 5 minutes



Result



Result



7. Hydrolysis of Pati Variables:  Control variable Volume of starch (amylum) solution Volume of benedict reagents Iodine test  Manipulation variable The addition of 2 ml of HCl 3 M, 2 ml of water and 3 ml of NaOH 3 M Heated in a water bath Cooled at room temperature  Response variable Changes that occur in all three solutions in the test tube Procedure



2 ml of pati (amylum) solution 1. Added 2 ml of HCl 3M 2. Heated in steam bath 3. Cooled in room temperature 4. Added 3 ml of NaOH 3M 5. Divided into 2 test tube 1b



1a 6. Iodine test



6. Added 5 ml of Benedict reagent



Result



Result



2 ml of pati (amylum) solution 1. Added 2 ml of water 2. Heated in steam bath 3. Cooled in room temperature 4. Added 3 ml of water 5. Divided into 2 test tube 2b



2a 6. Iodine test



Result



6. Added 5 ml of Benedict reagent



Result



2 ml of pati (amylum) solution 1. Added 2 ml of water 2. Let it in room temperature 3. Added 3 ml of water



3b



3a 4. Iodine test



Result



4. Added 5 ml of Benedict reagent



Result



Table 1.4.1 Molisch Test Observation Data No



Procedure



Observation Before



1



Test Tube 1







2,5 drops of Sucrose 1. Added 5 drops of Molisch reagent 2. Added 10 drops of concentrated Sulfuric acid until forms a separate layer from the initial layer If there is carbohydrate formed a red ring then turns dark purple







Sucrose :







2,5 drops of



colorless



sucrose + 5



solution



drops of



Molisch



molisch reagent



reagent :



: clear turbid



brownish



solution



solution 



After







2,5 drops of



H2SO4



sucrose + 5



concentrated :



drops of



colorless



molisch reagent



solution



+ 10 drops of concentrated H2SO4 : there



3. Leave for 2 minutes 4. Added 5 mL of water



are 2 layer (red



Purple formed



ring in lower layer) 



2,5 drops of sucrose + 5 drops of molisch reagent + 10 drops of concentrated H2SO4 + 5 mL of water : purple ring in solution



Test Tube 2







2,5 drops of Glucose 1. Added 5 drops of Molisch reagent 2. Added 10 drops of concentrated Sulfuric acid until forms a separate layer from the initial layer If there is carbohydrate formed a red ring then turns dark purple







Glucose :



2,5 drops of



colorless



glucose + 5



solution



drops of



Molisch



molisch reagent



reagent :



: clear turbid



brownish



solution



solution 











2,5 drops of



H2SO4



glucose + 5



concentrated :



drops of



colorless



molisch reagent



solution



+ 10 drops of concentrated



5. Leave for 2 minutes 6. Added 5 ml of water



H2SO4 : there are 2 layer (red



Purple formed



ring in lower layer) 



2,5 drops of glucose + 5 drops of molisch reagent + 10 drops of concentrated H2SO4 + 5 mL of water : purple ring in solution



Test tube 3







2,5 drops of Amylum 1. Added 5 drops of Molisch reagent 2. Added 10 drops of concentrated Sulfuric acid until forms a separate layer from the initial layer If there is carbohydrate formed a red ring then turns dark purple







Amylum :



2,5 drops of



colorless



amylum + 5



solution



drops of



Molisch



molisch reagent



reagent :



: clear turbid



brownish



solution



solution 











2,5 drops of



H2SO4



amylum + 5



concentrated :



drops of



colorless



molisch reagent



solution



+ 10 drops of concentrated



3. Leave for 2 minutes 4. Added 5 ml of water



H2SO4 : there are 2 layer (red



Purple formed



ring in lower layer) 



2,5 drops of amylum + 5 drops of molisch reagent + 10 drops of concentrated H2SO4 + 5 mL of water : purple ring in solution



Table 1.4.2 Seliwanof Observation Data No



Procedure



Observation Before



1



Test Tube 1







5 drops of amylum -



-



Added 5 drops of seliwanoff reagent Shake and heated the mixture on a water bath Note the time needed to colour changes







Amylum ,



After 



5 drops of



colorless



starch + 5 drops



solution



of seliwanoff



Seliwanoff



reagent, a



reagent, a



yellowish



yellowish



solution



solution







5 drops of starch + 5 drops of seliwanoff + reagent + heated,



Result



yellowish solution (does not change color) 



2 5 drops of lactose -



-



Added 5 drops of seliwanoff reagent Shake and heated the mixture on a water bath Note the time needed to colour changes



Result Test Tube 2







Lactose,



 5 drops Lactose +



colorless



5 drops



solution



seliwanoff



seliwanoff



reagent, a



reagent, a



yellowish



yellowish



solution



solution



 5 drops Lactose + 5 drops seliwanoff reagent + heated, yellowish solution (does not change color)



3



Test tube 2







5 drops of glucose -



-



Added 5 drops of seliwanoff reagent Shake and heated the mixture on a water bath Note the time needed to colour changes



Result







Glucose,







5 drops of



colorless



glucose + 5



solution



drops of



Seliwanoff



seliwanoff



reagent, a



reagent, a



yellowish



yellowish



solution



solution 



5 drops of glucose + 5 drops of seliwanoff reagent + heated, yellowish solution (does not change color



Table 1.4.3 Barfoed Test Observation Data NO 1



Line Work Test Tube 1 5 mL of Barfoed reagent



- Added 5 ml of amylum - Heated in a water bath - Wait for 2 minutes - Observed changes that occur



Result of observation Before



After



- Barfoed reagent : - Amylum + blue solution



Barfoed and



- Amylum:



heated : blue



Colorless solution



solution



- Lactose: Colorless solution - Glucose: Colorless solution



Result



- Wait for 10 minutes - Observed changes that occur Result Test Tube 2 5 mL of Barfoed reagent



- Glucose + Barfoed and heated : blue solution



- Added 5 ml of glucose - Heated in a water bath - Wait for 2 minutes - Observed changes that occur



Result



- Wait for 10 minutes - Observed changes that occur Result



Test Tube 3 5 mL of Barfoed reagent



- Lactose + Barfoed and heated : blue solution



- Added 5 ml of lactose - Heated in a water bath - Wait for 2 minutes - Observed changes that occur Result



- Wait for 10 minutes - Observed changes that occur Result



Table 1.4.4 Tollens Test Observation Data No



Observation



Treatment Test Tube 1



5 drops of Lactose Sample 1. Added 5 drops of Tollens reagent 2. Heated If no silver mirror is formed Result



Test Tube 2



5 drops of Sucrose Sample



Before     



Tollens reagent: colorless Lactose: colorless Sucrose: colorless Glucose: colorless Amylum: colorless



After 







 



1. Added 5 drops of Tollens reagent 2. Heated If no silver mirror is formed



Lactose + Tollens: brownish brown Lactose + Tollens + heated: silver mirror formed



Sucrose + Tollens: colorless Sucrose + Tollens + heated: silver mirror formed



Result Test Tube 3



5 drops of Glucose Sample 1. Added 5 drops of Tollens reagent 2. Heated If no silver mirror is formed Result







Glucose + Tollens: black Glucose + Tollens + heated: silver mirror formed



No



Treatment Test Tube 4



5 drops of Amylum Sample 1. Added 5 drops of Tollens reagent 2. Heated If no silver mirror is formed Result



Observation Before



After  Amylum + Tollens: pace brown  Amylum + Tollens + heated: colorless



Table 1.4.5 Fehling Test Observation Data No. 1.



Line Work Making Reagent Fehling Fehling A 1 mL 1. Add fehling B 1 Fehling reagent



Observation Result Before - Fehling



A



After : Fehling



A



+



Colorless



Fehling B : Blue



solution



solution



- Fehling



B



:



Blue solution 2.



Sucrose Test 2 drops of Sucrose 1. Add 2 drops of Fehling reagent Result



3.



Lactose Test 2 drops of Lactose 1. Add 2 drops of Fehling reagent Result



4.



Amylum Test 2 drops of Amylum 1.



Add 2 drops of Fehling reagent



Result 5.



Glucose Test 2 drops of Glucose 1. Add 2 drops of Fehling reagent Result



6.



Fructose Test



- Sucrose



: Sucrose + Fehling



Colorless



reagent



solution



solution



:



Blue



- Fehling reagent : Blue solution - Lactose



: Lactose + Fehling



Colorless



reagent



:



solution



precipitate



Red



- Fehling reagent : Blue solution - Amylum



: Amylum



+



Colorless



Fehling reagent :



solution



Blue solution



- Fehling reagent : Blue solution - Glucose



: Glucose



+



Colorless



Fehling reagent :



solution



Red precipitate



- Fehling reagent : Blue solution



- Fructose



: Fructose



+



No.



Line Work 2 drops of Fructose 1. Add 2 drops of Fehling reagent Result



Observation Result Before



After



Colorless



Fehling reagent :



solution



Red precipitate



- Fehling reagent : Blue solution



Table 1.4.6 Sucrose Hydrolysis Observation Data No.



Line work



1. 0,5 mL sucrose - Dissolved in water Sucrose solution



2.



Test tube 1



Result of Observation Before After - Sucrose : - Sucrose + aquades : colorless sucrose - Aquades : solution colorless



Test tube 1



Test tube 1



- Sucrose



-



Sucrose



1 mL Sucrose solution (1)



solution:



solution +



- Added 1 mL HCl 3 M



colorless



HCl



- Boiled in water bath



solution



solution



- Cooled at room temperature - Added 1,5 mL sucrose solution Test tube 1B Test tube 1A - Added 2 mL - Added 5 mL Benedict’s Seliwanof’s reagen reagen - Boiled in water bath for 5 - Boiled in water bath minutes for 5 minutes - Observed the changes that occur - Observed the changes that occur Result Result



- HCl solution



colorless :



colorless solution - NaOH



solution -



Sucrose solution + HCl



solution:



solution :



colorless



a. after



solution - Benedict reagent: blue solution -



:



Seliwanoff Reagen: colorless solution



heating : colorles s solutio n b. after heating and cooling : colorles s



solutio n -



sucrose solution + HCl solution + heating and cooling



+



NaOH solution



:



colorless solution Test tube 1a - solution in test tube 1 + benedict reagent



:



blue solution - solution in test tube 1 + benedict reagent



+



heating: blue greenish solution and



brick



red percipatate formed Test tube 1b



- solution in test tube 1+ Seliwanoff reagent



:



colorless solution -



solution in test



tube



1+ seliwanof reagen



+



heating: clear yellow solution. Test tube 2



Tabung 2



1 mL Sucrose solution (2)



-



- Added 1 mL water



solution



- Boiled in water bath - Cooled at room temperature



Test tube 2A



- Added 5 mL Benedict’s reagen - Boiled in water bath for 5 minutes - Observed the changes that occur



sucrose



Test tube 2B



- Added 2 mL Seliwanof’s reagen - Boiled in water bath for 5 minutes



Result



:



solution + aquades



solution



colorless



colorless



:



:



solution -



Sucrose



solution



solution +



- NaOH



aquades :



solution :



- After heating:



colorless



colorless



solution



solution



- Benedict Result



a. Sucrose



colorless



-aquades



- Added 1,5 mL sucrose solution



Tabung 2



Reagent : blue solution



-



After heating + cooling colorless solution



:



-



Seliwanoff Reagent : colorless solution



sucrose solution + aquades + heating and cooling + NaOH solution : colorless solution



-



sucrose solution + aquades + heating and cooling + NaOH



+



aquades: colorless solution Test tube 2a -



solution in test tube 1 + benedict reagent



:



blue solution -



solution in test tube 1 + benedict reagent + heating:



clear blue greenish solution and brick red precipitate formed Test tube 2b -



solution in test tube 1 + Seliwanoff reagent



:



colorless solution -



solution in test tube 1 + Seliwanoff reagent + heating clear yellow solution.



:



Test tube 3



-



Sucrose solution : colorless solution



-



Aquades : colorless solution



1 mL Sucrose solution (3) - Added 1 mL water - Cooled at room temperature - Added 1,5 mL water Test tube 3B



Test tube 3A



- Added 5 mL Benedict’s reagen - Boiled in water bath for 5 minutes - Observed the changes that occur Result



- Added 2 mL Seliwanof’s reagen



-



HCl : colorless solution



-



NaOH : colorless solution



-



Benedict Reagent : blue solution



-



Seliwanoff Reagent : colorless solution



- Boiled in water bath for 5 minutes



- Observed the changes that occur Result



Test tube 3 Sucrose solution + aquades : colorless solution -



-



-



-



Sucrose solution + aquades + placed at room temperatur e: colorless solution Sucrose solution + aquades + placed at room temperatur e + aquades : colorless solution Test tube 3a Solution in test tube 3 + R. Benedict : blue solution



- Solution in test tube 3 + Benedict reagent + heating : blue greenish solution Test tube 3b - Solution in test tube 3+



aquades : colorless solution -



Solution in test tube 3+ aquades + placed at room temperatur e: colorless solution



-



Solution in test tube 3+ aquades + placed at room temperatur e+ aquades : colorless solution



-



Solution in test tube 3+ aquades + placed at room temperatur e+ aquades+ Seliwanoff R: clear yellow solution



-



Solution in test tube 3+ aquades + placed at room temperatur



e+ aquades+ Seliwanoff R+ heating : clear yellow solution



Table 1.4.7 Pati Hydrolysis Observation Data No.



Observation



Treatment



1.



Before



-



Tube 1



Starch



After



-



2 mL



Solution:



Starch



Colorless



solution + 2



solution



mL HCl



HCl



solution =



2. Put the tube on the water bath



solution:



Colorless



3. Cooled at room temperature



Colorless



solution.



4. Add 3 mL of NaOH 3 M



solution



2 mL of starch solution 1. Added 2 mL of 3 M HCl solution



-



-



-



Put on a



3 M NaOH



water bath



Divided the solution into 2



Solution:



= colorless



tubes with the same volume



Colorless



solution



Solution



Tube 1A



5. Add enough iodine Result



Solution Tube 1B



-



6. Put 5 mL of benedict reagent



-



+ 3 mL



Iodine



NaOH =



Solution:



colorless



yellowish



solution



brown Result



-



-



Solution 1A



Benedict



+ Iodine =



reagent:



Colorless



blue



solution



solution



-



Solution 1B + 5 mL Benedict reagent = Blue solution



2.



-



Tube 2 2 mL of starch solution 1. Added 2 mL of water 2. Put the tube on the water bath 3. Leave it at room temperature 4. Add 3 mL of water



-



Divided the solution into 2 tubes with the same volume Tube 2A 5. Add enough iodine



Result



6. Enter 5 mL of benedict reagent



Result



-



2 mL Starch



Colorless



solution + 2



solution



mL Water =



Water: A



colorless



colorless



solution -



Put on



Iodine



water bath



Solution:



= colorless



yellowish



solution



brown Tube 2B



-



Solution:



solution -



Solution



Starch



-



Refrigerate



Benedict



d at room



reagent:



temperature



blue



= Colorless



solution



solution -



+ 3 mL Water = Colorless solution



-



Solution 2A + Iodine = Blue solution



-



Solution 2B + 5 mL Benedict reagent = Blue solution



3.



- Starch



-



2 mL



Tube 3



Solution:



Starch



2 mL of starch solution



Colorless



solution +



solution



2 mL



1. Added 2 mL of water 2. Leave it at room temperature 3. Add 3 mL of water



- Water: colorless



colorless



solution



solution.



- Iodine Solution Divided the solution into 2 tubes with the same volume



Tube 3A 4. Add enough iodine



Result



Tube 3B 5. Put 5 mL of benedict reagent



Water =



-



Leave it at



Solution:



room



yellowish



temperatur



brown



e=



- Benedict



colorless



reagent: blue



solution -



solution



+ 3 mL Water = Colorless



Result



solution -



Solution 3A +



Iodine = Dark blue solution -



3B solution + 5 mL Benedict reagent = Blue solution



Task 5 1. Molisch Test a. Reaction The reaction is as follows: Sucrose reaction



Sucrose



Glucose



5-hydroxymethyl furfural



Purple compound



Fructose



α-naphthol



Purple compound



1) Glucose reaction



Glucose



5-hydroxymethyl furfural



α-naphthol



Purple compound 2) Reaction Starch



Starch



Glucose



Purple compound 3) Fruktosa Reaction



Glucose



5-hydroxymethyl furfural



naftol



Purple compound



4) Lactose Reaction



Lactose



5-hydroxymethyl furfural



-naftol



Purple compound b. Explanation In this experiment we applied the principle of molisch test. The principle of the molisch test is a reaction of carbohydrate dehydration by sulfuric acid or H2SO4 to form a complementary ring or hydroxyl methyl hydroxide when reacting with α-naftol present in the reagent. If in the snippet there is a carbohydrate, a red ring will form on the bottom layer. The red will soon turn into a dark purple. Once dried and diluted with water it will turn purple. First, the extracts (sucrose, glucose, and amylum) were added for 2-5 drops and 5 drops of Molisch reaction. Then put 7-10 drops of concentrated sulfuric acid into the base of the tube with a drop of pipes in such a way that sulfuric acid forms a separate layer from the initial layer. Addition of sulfuric acid (H2SO4) to



hydrolyze polysaccharide (amylum) and produce furfural. Because strong acids (H2SO4) cause hydrolysis of some polysaccharides and strong acids can react with a solution containing monosaccharides (sucrose and glucose) to produce furfural or its derivatives. When



sucrose



is



added



to



the



molisch



reaction,



the



sucrose is hydrolyzed by concentrated H2SO4 to appear in red sediment until finally dark purple. The dark purple color indicates that the trailer is a carbohydrate (positive test). Sucrose is a disaccharide of glucose and fructose When glucose is added to the molisch reaction, the mixture of glucose and the reaction of molisch (α-naftol) and reacted with concentrated H2SO4 will produce furfural hydroxymethyl until it forms a reddish-brown color first, eventually turning purple. Dark purple indicates that glucose is a monosaccharide-based carbohydrate (positive test). When amylum is added to the molisch reaction, the amylum and molish reaction (α-naftol) and reacted with concentrated H2SO4 will be hydrolyzed to appear red and eventually turn purple. Blackish purple indicates that amylum is a carbohydrate, a polysaccharide (positive test) Sucrose, glucose, and amylum showed a positive test with the addition



of



a



molisch



reaction



that



identified



all



three



as



carbohydrates. With the addition of concentrated H2SO4 will hydrolyze carbohydrates from the form of polysaccharides/disaccharides into monosaccharides. 2. Seliwanof Test a. Reaction In the test tube 1 (Amylum)



n + n H2O



H+



H+, O (can’t react)



2n



Resorsinol



Glucose In the test tube 2 (Lactose)



H2O, H+



H+, O (can’t react) Resorcinol



In the test tube 3 (Glucose)



H2O, H+



H+, O (can’t react) Resorcinol b. Explanation In this experiment there are 3 samples that will be tested seliwanof they are amylum, lactose, and glucose. The first step is to prepare the tools and materials needed, for the materials needed are seliwanoff, amylum, lactose, glucose, aquades, methylated reagents, while the tools that are needed are test tubes, pipettes, beaker , test tube racks. In the first experiment 5 drops of yellow wish seliwanof reagent solution were added then 5 drops of colorless amylum solution. Then shake it, then heat it in the water heated. Note the time needed to colour change. The solution does not change color. This indicates that amylum does not contain ketone groups, so they do not change color and give negative test results. In the second experiment 5 drops of yellow wish seliwanof reagent solution were added, and 5 drops of colorless lactose solution were added. Then shake the solution, then heated it in water bath. Note the time needed to colour change. The solution does not change. This indicates that glucose does not contain ketone groups, so it does not change color, and gives negative test results. The last, in the third experiment 5 drops of yellow wish seliwanof reagent solution were added, then 5 drops of colorless glucose solutin. Then shake the solution, then heat it in the heated. Note the time needed to colour change. The solution does not change. This indicates that glucose does not contain ketone groups, so it does not change color, and gives negative test results. 3. Barfoed Test a. Reaction Amylum



Glucose



Fructose



Sucrose



Cu(CH3COO)2 CH3COOH



Lactose



Cu(CH3COO)2 CH3COOH



(aq) b. Explanation After heating a dark blue solution was formed in each tube, and after heating> 10 minutes of starch and lactose did not form a brick red precipitate, but in glucose formed a brick red precipitate. This shows that glucose is a monosaccharide, where monosaccharides quickly reduce Cu (II) ions from Barfoed reagents to Cu (I). The red brick deposits formed are Cu2O deposits.



The principle is the reduction of Cu2 + found in barfoed reagents by the reducing group on monocasarida in acidic conditions. A positive reaction is indicated by the appearance of an orange-red or brick-red example. In the barfoed glucose test, fructose, lactose and sucrose react positively which is marked by the presence of red brick deposits after heating. So that glucose, fructose, lactose, and sucrose are reducing monosaccharide sugars as in the literature which states that the Bafoed test is used to test the presence of reducing monosaccharide sugars. 4. Tollens Test a. Reaction Making of tollens reagents: 



2AgNO3 (aq) + 2NaOH (aq) → AgO (s) + 2NaNO3 (aq) + H2O (l)







Ag2O (s) + NH4OH (aq) → 2Ag(NH3)2OH (aq) + 3H2O (l)



Tollens test: The tollens test is positive if silver mirrors are formed which indicate the presence of reducing sugars Sucrose



+







(aq)



(aq) + 2Ag(NH3)2OH (aq) →



(aq) + 2Ag(s) silver mirror + NH3 (aq)







(aq) + 2Ag(NH3)2OH (aq) →



(aq) + 2Ag (s) silver mirror + NH3 (aq) Amylum



n (aq) + 2Ag(NH3)2OH (aq) Lactose



(aq)



(aq) +



2Ag(NH3)2OH (aq) + 2Ag (s) silver mirror + NH3 (aq) Glucose



(aq)



(aq) + 2Ag(NH3)2OH (aq) →



(aq) + 2Ag(s) silver mirror + NH3 (aq) Fructose



(aq) + 2Ag(NH3)2OH (aq) →



(aq) + 2Ag (s) silver mirror + NH3 (aq)



b. Explanation The fourth experiment is the tollens test. The purpose of the tollens test is to identify the presence of reducing sugars in carbohydrates. Aldehyde groups in all aldose species can be oxidized by weak oxidizing agents such as tollens (Hidajati, et al, 2019). The reduction from Ag + to Ag by reducing sugars is characterized by the formation of a silver mirror (Ag) and oxidizes the aldehyde group to the carboxylate group. A positive reaction by Tollens reagents is characterized by the formation of a silver mirror that shows a positive test for reducing sugars. Tests on Tollens reagents are based on the ease of aldehyde groups formed from reversible reactions of cyclic hemiasetal monosaccharides (Matsjeh et al, 1996). In the tollens test there are four carbohydrates to be tested, namely sucrose, starch, lactose and glucose. Each of these substances is inserted into each test tube. Test tube A contains sucrose, test tube B contains starch, test tube C contains lactose, and test tube D contains glucose. After that, each test tube drops 5 drops of tollens reagents that have been made earlier. Test tube A, the addition of a colorless solution tollens reagent to sucrose a colorless solution forming a silver mirror according to the theory shows that sucrose contains a reducing group. Sucrose is hydrolyzed into monosaccharides namely glucose and fructose. Tollens reagents will be reduced by monosaccharides both glucose and fructose from +1 to 0 so that the Ag deposits or commonly known as silver mirrors will be obtained.



Test Tube B, the addition of the colorless reagent tollens reagents to starch. The colorless solution is not formed silver mirror only brown solution, because starch has hemiasetal at one end of the molecule, but this end is only a small part of the whole starch molecule, so it does not affect the reaction. As a result, starch cannot reduce tollens reagents. This shows that starch is not a reducing sugar. Test tube C, the addition of the colorless reagent tollens reagent to the lactose of the colorless solution formed silver mirror according to the theory it shows that lactose is a reducing sugar. Lactose is hydrolyzed into monosaccharides namely glucose and galactose. Glucose and galactose which contain aldose groups and are reducing sugars can reduce Ag + charged + 1 from toll reagent to Ag neutral atom which has 0 charge to form silver mirror. Test Tube D, the addition of colorless solution tollens reagents to glucose colorless solution formed silver mirror according to the theory it shows that lactose is a reducing sugar. Glucose is a reducing sugar, glucose has an aldose group that can reduce Ag + from toll reagent reagents to Ag to form a silver mirror. Thus, substances containing reducing sugars are shown by the formation of silver mirrors namely glucose, sucrose, and lactose 5. Fehling Test a. Reaction Reaction of Fehling Test a. Lactose



+ 2Cu2+ + 5OH- 



b. Sucrose



+ Cu2O  + 3H2O



+ 2Cu2+ + 5OH-







c. Glucose



+ Cu2O  + 3H2O



+ 2Cu2+ + 5OH-  d. Fructose OH



+ 2Cu2+ + 5OH- 



+ Cu2O  + 3H2O



e. Amylum



+ 2Cu2+ + 5OH-







b. Explanation This experiment has the purpose to identify the presence of reducing sugar in the sample through the fehling test. This test is based on the reactivity of the substance to be oxidized against weak oxidizing agents. The principle of the fehling test is the ability of a sample containing reducing sugars to reduce a



fehling reagent containing Cu2+ ions to Cuions+ which is characterized by the formation of red brick deposits in the sample. Red brick deposits occur due to Cu2+ ions which are reduced by the aldehyde or ketone groups contained in the sample (Fessenden, 1992). Fehling reagents are made from a mixture of Fehling A and Fehling B. Fehling A (34.65 grams of copper sulfate in 500 ml of water) and Fehling B (a mixture of 173 grams of sodium hydroxisa and 125 grams of potassium sodium tartrate in 500 mL of water). The mixture of Fehling A solution and Fehling B solution is a blue solution (Sumardjo, 2009). The work step in this experiment is that 2 drops of sample are added with 2-3 ml of Fehling's solution. Then shake and heat it on a water bath for 3-4 minutes. In this experiment there were 4 samples, namely starch, lactose, sucrose and glucose in 4 different test tubes. a) Test tube 1. Starch 2 drops of colorless starch are put into a test tube and added with 2-3 ml of fehling solution. The solution will be blue. After it is shaken and heated, starch does not produce brick red deposits. This is because starch is not a reducing sugar. Although starch has an unsubstituted anomeric C atom at the end of the chain, the size of the starch molecule is not proportional to the size of Cu2+ (in the Fehling reagent), so the possibility of reaction is very small. So for the Fehling test on starch negative. b) Test tube 2. Lactose 2 drops of colorless lactose are inserted into the test tube and added with 2-3 ml of fehling solution. The solution will be blue. After being shaken and heated, lactose will produce brick red deposits. Deposition occurs because anomeric C atoms in lactose and glucose have not been substituted in the sense that OH groups bound to anomeric C atoms are still free to move from the alpha (α) to beta (β) position or the molecule undergoes mutarotation. When mutarotation occurs, the chain structure will open (previously closed). It is during this open chain that the Fehling reagent can oxidize the aldehyde group on the anomeric C atom. This is what causes the Fehling reagent to oxidize aldose groups in lactose and glucose



which is characterized by the formation of brick red deposits (Cu2O) which is the result of reduction of the Fehling reagent. So lactose is a reducing sugar. c) Test tube 3. Sucrose 2 drops of colorless sucrose are inserted into a test tube and added with 2-3 ml of fehling solution. The solution will be blue. After being shaken and heated, sucrose will not produce brick red deposits. Test results are negative. This shows that sucrose is not a reducing sugar. The size of the sucrose molecule is not proportional to the size of Cu2+ (in the Fehling reagent) so the possibility of reacting is very small. So that no red deposits are formed. d) Test tube 4. Glucose 2 drops of colorless glucose are inserted into a test tube and added with 23 ml of fehling solution. The solution will be blue. After being shaken and heated, glucose will produce brick red deposits. The aldehyde group contained in the sample when in water is in equilibrium with the open chain aldehyde form, so as to reduce Cu2+ ions by forming Cu2O compounds in the form of red deposits. Glucose is reducing sugar. 6. Sucrose hydrolysis a. Reaction Test tube 1



+



H+, OHSucrose Test tube 1A Glucose



Glucose



Fructose



(aq) + 2Cu2+ (aq) + 5OH-







(aq) + Cu2O



(s) + 3H2O Fructose



(aq) + 2Cu2+ 5OH- 



(aq) + Cu2O (s)



+ 3H2O Test tube 1B 3H2O, H+



Cherry Red Test tube 2



H+, O, SO2



+



H+, OHSucrose



Glucose



Fructose



Test tube 2A Glucose



(aq) + 2Cu2+ (aq) + 5OH- 



(aq) + Cu2O



(s)+ 3H2O Fructose



(aq) + 2Cu2+  3H2O Test tube 2B



(aq) + Cu2O (s) +



H+, O, SO2



3H2O, H+



Cherry Red Test tube 3



+ H2O



Test tube 3A Benedict test



+ Cu22- (citrate)



Test tube 3B Seliwanoff test



H2 O



[H+]



b. Explanation Sucrose is a type of disaccharide carbohydrate consisting of two monosaccharides namely fructose and glucose. Both of them bind to C atom number 1 to glucose and number 2 to fructose to form a 1,2-βglycosidic linkage. The anomeric C atom in sucrose has been substituted so that it cannot reduce Benedict's reagent. However, in an acidic and warming atmosphere sucrose will be completely hydrolyzed or sugar inversion will form into glucose and fructose. So that the test with Benedict and seliwanoff will be positive, where Benedict's reagent will reduce glucose hydrolysis results and red brick deposits are produced. While the fructose seliwanof test results from hydrolysis will be detected to form a cherry red solution. While the success in addition to hot water will also experience a hydrolysis reaction, but the reaction is not as great as the addition of acids so that the hydrolysis reaction in the addition of hot water is a partial hydrolysis reaction. While the addition of cold water does not occur hydrolysis reaction. Hydrolysis of sucrose in addition to acids and heating, addition of hot water, and the addition of results obtained as follows: Compound



Sucrose



Addition



Reagent



Reagent



HCl + heating



Benedict



Seliwanoff



+



+



Hydrolysis occurs



+ = brick red precipitate (green solution) formed in benedict and cherry red solution formed in seliwanof - = no red brick deposits (green solution) were formed on benedict and not a cherry red solution formed in seliwanof.



In the results of experiments with the addition of acid followed by heating obtained positive tests with benedict and seliwanoff reagents which indicate that hydrolysis of sucrose to glucose and fructose occurs. This is in accordance with the theory. Compound



Addition Hot



Reagent



Reagent



water



Benedict



Seliwanoff



-



-



Partial Sucrose



hydrolysis occurred



+ = brick red precipitate (green solution) formed in benedict and cherry red solution formed in seliwanof - = no red brick deposits (green solution) were formed in the benedict and no red cherry solutions in the seliwanof form



In the results of experiments with the addition of hot water followed by heating obtained negative tests with benedict and seliwanoff reagents which indicate that there is no hydrolysis of sucrose to glucose and fructose. This is not in accordance with the theory. This is because the hydrolysis with hot water takes a long time so that it may take less time to warm up so that hydrolysis has not occurred. Compound



Sucrose



Addition



Reagent



Reagent



Cold water



Benedict



Seliwanoff



-



-



No hydrolysis occurs



+ = brick red precipitate (green solution) formed in benedict andncherry red solution formed in seliwanof - = no red brick deposits (green solution) were formed on benedict and not a cherry red solution formed in seliwanof



On the hypothesized experiment with the addition of cold water, negative tests were obtained with benedict and seliwanoff reagents which indicated that hydrolysis did not occur with sucrose to glucose



and fructose. This is consistent with the theory that the addition of cold water does not occur hydrolysis. 7. Pati Hydrolysis a. Reaction Test tube 1



n+ H+, OH-







Test tube 1A



+ I2 



Test tube 1B



+ Cu2+ (aq) → 



(aq) + Cu2O (s) + 3H2O (l)



Test tube 2



H2O



n+ 



Test tube 2A



+ n I2 →



n + 2 H2O (l)







Test tube 2B



n + Cu2+ (aq) 



Test tube 3



H2O



n+ 



Test tube 3A



+ n I2 →



n + 2 H2O (l) 



Test tube 3B



n + Cu2+ (aq) b. Explanation This experiment has purpose to produce glucose, maltose, dekstrin that test with iodin and benedict. To check polysaccharides in sample using iodine test, and to distinguish between aldose and ketose sugar in carbohydrates. The hydrolysis reaction of amylum involves water as a reductor. To observe the ongoing hydrolysis reaction can be tested with iodine. Iodine will react if the sample still contain amylum and cause the color of the solution to turn into blackish purple. To test the hydrolyzed amylum into glucose, benedict’s test can be performed, which show the sample turns blue and there is a red brick deposit at the bottom of the tube.



1) Test tube 1 First step is 2 ml of amylum solution added by 2 ml of HCl 3M. This way of addition concentrated acid is to hydrolyzed the amylum and also break the amylum’s structure because it has corrosive characteristic. Then steamed in the waterbath. After that cooled it down, continue with added 3 ml NaOH 3M, the result is colorless solution. The reaction is : Test tube 1



n+



H+, OH-



Then separate into 2 test tube with the same volume, which labelled by 1a and 1b, then test tube 1a added 1 drop of iodin which has brown colour, the result is the colour still colorless. It indicate that amylum was not hydrolized. This because iod reacts with basic solution so it does not reacts with amylum. This situation occurs because the presence of NaOH in the solution reacts with iod formed NaI and NaOI, so that in the test with the addition of NaOH, there is no change in the solution of amylum. The reaction is : Test tube 1A



+ I2 For test tube 1b, added by 3 drops of benedict reagent. The solution become electric blue solution. Next, heated it. The result is the formed brick red precipitate. This means, test tube 1b is perfectly-hydrolyzed. The reaction that occur is: Test tube 1B



+ Cu2+ (aq) →



(aq) + Cu2O (s) + 3H2O (l)



2) Test tube 2 For the second test tube, the first step is 2 ml of amylum solution added by 2 mL of aquadest then steamed for a while in the waterbath in order to hydrolyzed the amylum. After that cooled it down, then continue added 3 mL of aquadest again and separated into two different test tube with the same volume, which labelled by 2a and 2b. The reaction that occur is: Test tube 2



H2O



n+ For test tube 2a, added 1 drop of iodin which has brown colour, then the solution changed from colorless into dark-purple solution. The reaction that occurs is : Test tube 2A



+ n I2 →



n + 2 H2O (l) And for test tube 2b, added 1 mL of Benedict reagent then heated it. The solution become darker than before which is light blue solution and no precipitate formed. It indicate that there is no hydrolize process that occur. The reaction that occurs is :



Test tube 2B



n + Cu2+ (aq) 3) Test tube 3 For the third tube, the first step is 2 ml of amylum solution added by 2 mL aquades like test tube 2 but no heating process. Then, added again with 3 mL aquades and heated in the waterbath. The reaction that occurs is : Test tube 3 H2O



n+ Next, amylum solution after added aquadest divided into two different test tube with the same volume then labelled with 3a and 3b. For test tube 3a, added 1 drop of iodin which has brown colour, then the solution changed from colorless into dark-purple solution (++) solution. The reaction that occurs is : Test tube 3A



+ n I2 →



n + 2 H2O (l) But in test tube 3b, added by 1 mL of Benedict’s reagent, the solution become electric blue solution. Next, heated it. The result is there is no brick red precipitate formed. The reaction can write with : Test tube 3B



n + Cu2+ (aq)



Conclusion Based of the data experiment, it can concluded that: 1.



Molisch test aims to prove the existence of carbohydrates. The Molisch test shows that sucrose, glucose, and amylum are carbohydrates that indicate by forming purple colour



2.



Seliwanoff test aims to prove the existence of ketoses. Seliwanoff's test shows that in amylum, lactose and glucose there are no ketose groups that indicate by no colour changes



3.



Barfoed test aims to distinguish between monosaccharides and disaccharides. The Barfoed test shows that glucose and lactose is classified as monosaccharide, whereas amylum is disaccharides that indicate by forming red precipitate



4.



Tollens test aims to show the presence of reducing sugars in carbohydrates. From the Tollens test it can be concluded that sucrose, glucose, and lactose are reducing sugars that indicate by forming silver mirror



5.



Fehling test aims to determine the presence of aldose groups on carbohydrates, or test the presence of reducing sugars in carbohydrates. From the Fehling test it can be seen that lactose and glucose have aldose groups which can reduce fehling which is characterized by the formation of brick red deposits.



6.



To test the results of sucrose hydrolysis which is glucose and fructose, used benedict test or seliwanof test. The test show that tes tube 1 and 2 produce glucose and fructose which is indicated by the formation of brick red precipitate. A positive test in the seliwanoff test is indicated by the formation of an orange red color.



7.



The iodine test can be used to test the hydrolysis results in starch. The test show that tes tube 1 and 2 with iodine produce glucose and fructose which is indicated by the formation of dark blue solution, with formed light blue solution.