Explain the role of the starch iodide test during the oxidation reaction and explain the reaction that was used to identify the formation of the product in that reaction.
*The experiment was Cyclohexanone from Cyclohexanol: Cyclohexanol + NaCl-----Acetic Acid---> Cyclohexanone + NaCl + H2O
The starch iodide test is a common chemical test used to detect the presence of free iodine in a solution. In the context of the given reaction involving the conversion of cyclohexanol to cyclohexanone, the starch iodide test is used to identify the formation of iodine, which is an intermediate product in the reaction.
The oxidation of cyclohexanol to cyclohexanone involves the use of a strong oxidizing agent, such as sodium hypochlorite (NaCl) in the presence of acetic acid (CH3COOH). The reaction can be represented as follows:
Cyclohexanol + NaCl (sodium hypochlorite) → Acetic Acid → Cyclohexanone + NaCl + H2O
During the oxidation process, cyclohexanol is converted to cyclohexanone, and a key intermediate in this reaction is the formation of iodine (I2) from the reaction of sodium hypochlorite and acetic acid. The presence of free iodine is a characteristic feature of the reaction, and this is where the starch iodide test comes into play.
The starch iodide test is based on the fact that iodine molecules can form a blue-black complex with starch molecules. In the absence of free iodine, the starch iodide test solution remains colorless. However, if free iodine is present, it reacts with the starch in the test solution to produce the blue-black complex, indicating the formation of iodine.
The test is performed by adding a few drops of the starch iodide test solution to the reaction mixture after the oxidation reaction has taken place. If the reaction has been successful and free iodine has been formed, the test solution will turn blue-black, confirming the presence of iodine, which is an intermediate product in the oxidation of cyclohexanol to cyclohexanone.
Overall, the starch iodide test is a useful tool in organic chemistry for detecting the presence of iodine and confirming the progress of oxidation reactions like the one described in the experiment.
Explain the role of the starch iodide test during the oxidation reaction and explain the reaction...
What is the role of the Acetic acid in the oxidation of Cyclohexanol to Cyclohexanone? Write the balanced chemical reaction between acetic acid and sodium hypochlorite.
1. What is oxone?
2. When preforming a chemical test to check that the oxidant was
fully quenched, we used potassium iodide and two drops of acetic
acid mix with the aqueous layer of an oxidation reaction solution
form (-) borneal to boreone. What chemical was resonsible for the
dark brown color that is indicative of a positive test?
3. We have called this oxidation green. What does the term mean,
and in which way can we say that the...
Explain the process happened during iodine test on acid-hydrolyzed starch and what colour do it produced at the end of the experiment
someone help me with these 7 questions
add a drop of iodine solution. If starch is present, I Wl iodine. The starch-iodine complex is deep blue-violet. Repeat this test with a com- mercial aspirin tablet and with the acetylsalicylic acid prepared in this experiment O N S at is the purpose of the concentrated phosphoric acid used in the first step? What would happen if the phosphoric acid were left out? 2. 1. Wh 3. If you used 250 mg...
[08 pts.] Briefly explain the roles of sodium hypochlorite and acetic acid in the oxidation of cyclohexanol. sodium hypochlorite and acetic aut are added together to create the hypochlurous act, which used to protorate the oth grap on cyclo hexarod. [12 pts.] Draw the major product for each of the following oxidation reactions. кон Na CrO; H2SO4, H,0 Na Cr2O7 H2SO4, H20 CHO PCC
Why is it important to keep the temperature between 35-40 degree C during the oxidation reaction? what could happen if the temperature is too low? Too high? For this case we are producing cyclohexanone by using bleach and cyclohexanol Thank you:)
What is the general class of each test reaction in the introduction? Precipitation? Acid-Base? Oxidation eduction? anoina to aizy ona svidstils Reaction Class 1 2 iliw 15 TO15192do art sshommua bns nosgol rond dass 101 12575 gbubnium oY noi de lo enor Som 10 910 w II woy Xd on abian aningstid on naloga uzib 3 OOH 4 5 DHET 6 7 SET adus 00 9 Complex ion formation 10 11 No reaction 12 13 14 Combination 15 16 17...
chemical reaction 4. Which Cyclohexanol oxidation method is "cleaner" (safer for the environment): the one using dichromate or the one using Clorox? Why (answer in terms of the waste products generated in these reactions)? 5. Why did we extract the Cyclohexanone in a three step extraction (with 10 ml, 8 ml and 7 ml Ether) rather than in one step (with 25 ml Ether)? 6. What does it mean if the IR spectrum of your final product (Cyclohexanone) shows a...
Oxidation of Cyclohexanol to Adipic Acid (continued on the next page): (1) (2 pts) In this experiment we could have used cylcohexene instead of cyclohexanol and we would have still gotten adipic acid. Draw an alkene and an alcohol each of which would react with nitric acid to give suberic acid. (4 pts) In the oxidation that you carried out in this experiment, nitric acid ends up as a mixture of oxides of nitrogen. Use the formula index of the...
1 - Provide a balanced equation for this reaction
2 - Provide a mechanism for the transformation of cyclohexanol
into cyclohexanone
3 - Provide a flow chart for the workup procedure for isolating
cyclohexane from all the by-products, making sure to note in which
layer you expect to find your product in each extraction.
4 - Provide the theoretical yield of cyclohexane in this
experiment.
PROCEDURE OXIDATION OF CYCLOHEXANOL TO CYCLOHEXANONE Set up a water bath as the heat source...