If you oxidized a compound containing an aldehyde, what qualitative test would you use to determine...
If you oxidized a compound containing an aldehyde, what qualitative test would you use to determine if the product is good or bad?
Homework Answers
If you oxidized a compound containing an aldehyde, you the aldehyde will be converted into a carboxylic acid.
Three tests can be performed to know whether the product is good or bad.
i) Litmus Test. Carboxylic acid turns blue litmus red.
ii) Sodium Hydrogen Carbonate Test. Carboxylic acid reacts with sodium hydrogen carbonate to produce carbon dioxide gas which can be seen in the form of a brisk effervescence.
iii) Ester Test.
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If you oxidized a compound containing an aldehyde, what
qualitative test would you use to determine...
If you reduce a compound containing an aldehyde, what qualitative test would you use to determine...
If you reduce a compound containing an aldehyde, what qualitative test would you use to determine if the product is good or bad?
2. Be able to decide when to use sodium borohydride and when to use lithium aluminum...
2. Be able to decide when to use sodium borohydride and when to use lithium aluminum hydride for reducing an aldehyde. 3. If you reduce a compound containing an aldehyde, what qualitative test would you use to determine if the product is good or bad? 4. Draw the mechanism for the reduction of vanillin vanillyl alcohol. Oxidation of an Aldehyde (Vanillin III) 5. Be able to determine the oxidation of carbon in different molecules. 6. Write the mechanism for this...
1.) What would the product be if you oxidized a tertiary alcohol? A.) Ketone B.) Aldehyde...
1.) What would the product be if you oxidized a tertiary
alcohol?
A.) Ketone
B.) Aldehyde
C.)Carboxylic Acid
D.) No reaction
2.) What would the FULLY oxidized product of a primary alcohol
be?
A.) No reaction
B.) Carboxylic Acid
C.) Aldehyde
D.) Ketone
3.) Which types of alcohol can be oxidized? Choose all that
apply.
A.) Quaternary
B.) Primary
C.) Secondary
D.) Tertiary
4.) the Ethanol standard in test tube 3 will have a final
concentration of _____%(v/v) ethanol.
5.)...
What chemical test (reaction) could you use to determine whether or not an aldehyde is present...
What chemical test (reaction) could you use to determine whether or not an aldehyde is present in a molecule? (2 pts bonus)
3. Suggest a qualitative test (based on solubility) that would differentiate a pure acidic organic compound...
3. Suggest a qualitative test (based on solubility) that would differentiate a pure acidic organic compound from a neutral organic compound. Indicate clearly how the test would be done: steps to be taken, what result would be expected for an acidic compound vs. a neutral compounds. Hint: lab 2 contained a series of qualitative tests. Qualitative solubility tests give different (visible) results for different types of compounds. Complete on a separate page, please
synthsis of asprin 6. Iron(III) ions are used as a qualitative test for phenols (aromatic compounds...
synthsis of asprin
6. Iron(III) ions are used as a qualitative test for phenols (aromatic compounds containing an -OH functional group). (1 point) a. What compound was used as a positive control for the Fe3+ test in this experiment? b. Did the reaction product give a positive or negative test with Fetions? Explain. 6. Iron(III) ions are used as a qualitative test for phenols (aromatic compounds containing an-OH functional group). (1 point) a. What compound was used as a positive...
5. Iron(III) ions are used as a qualitative test for phenols (aromatic compounds containing an-OH functional group)...
5. Iron(III) ions are used as a qualitative test for phenols (aromatic compounds containing an-OH functional group). (1 point) a. What compound was used as a positive control for the Fe3+ test in this experiment? b. Did the reaction product give a positive or negative test with Fe3+ ions? Explain. 6. Acetic anhydride was used in excess in this experiment. What does this mean, and how was the excess acetic anhydride decomposed at the end of the reaction? (1 point)
11. What would be the test widely use to know whether I have an Aldehyde and...
11. What would be the test widely use to know whether I have an Aldehyde and why? (2pts) 12. What happens if I add HCl to a tertiary amine? Why? (2pts)
Please help 4 and 5. Will rate. 4. For the reaction below, draw the intermedi ate...
Please help 4 and 5. Will rate.
4. For the reaction below, draw the intermedi ate before the addition of HCle? WUCHO D HCI/10 5. What test from the Qualitative Analysis of Functional Groups would you use to determine if vanillin has been successfully reacted to form a new product in which the aldehyde group of vanillin has been oxidized?
What would the FULLY oxidized product of a primary alcohol be? Question 1 options: Carboxylic Acid...
What would the FULLY oxidized product of a primary alcohol be? Question 1 options: Carboxylic Acid Aldehyde No reaction Ketone
2. Be able to decide when to use sodium borohydride and when to use lithium aluminum hydride for reducing an aldehyde. 3. If you reduce a compound containing an aldehyde, what qualitative test would you use to determine if the product is good or bad? 4. Draw the mechanism for the reduction of vanillin vanillyl alcohol. Oxidation of an Aldehyde (Vanillin III) 5. Be able to determine the oxidation of carbon in different molecules. 6. Write the mechanism for this...
1.) What would the product be if you oxidized a tertiary
alcohol?
A.) Ketone
B.) Aldehyde
C.)Carboxylic Acid
D.) No reaction
2.) What would the FULLY oxidized product of a primary alcohol
be?
A.) No reaction
B.) Carboxylic Acid
C.) Aldehyde
D.) Ketone
3.) Which types of alcohol can be oxidized? Choose all that
apply.
A.) Quaternary
B.) Primary
C.) Secondary
D.) Tertiary
4.) the Ethanol standard in test tube 3 will have a final
concentration of _____%(v/v) ethanol.
5.)...
What chemical test (reaction) could you use to determine whether or not an aldehyde is present in a molecule? (2 pts bonus)
3. Suggest a qualitative test (based on solubility) that would differentiate a pure acidic organic compound from a neutral organic compound. Indicate clearly how the test would be done: steps to be taken, what result would be expected for an acidic compound vs. a neutral compounds. Hint: lab 2 contained a series of qualitative tests. Qualitative solubility tests give different (visible) results for different types of compounds. Complete on a separate page, please
synthsis of asprin
6. Iron(III) ions are used as a qualitative test for phenols (aromatic compounds containing an -OH functional group). (1 point) a. What compound was used as a positive control for the Fe3+ test in this experiment? b. Did the reaction product give a positive or negative test with Fetions? Explain. 6. Iron(III) ions are used as a qualitative test for phenols (aromatic compounds containing an-OH functional group). (1 point) a. What compound was used as a positive...
5. Iron(III) ions are used as a qualitative test for phenols (aromatic compounds containing an-OH functional group). (1 point) a. What compound was used as a positive control for the Fe3+ test in this experiment? b. Did the reaction product give a positive or negative test with Fe3+ ions? Explain. 6. Acetic anhydride was used in excess in this experiment. What does this mean, and how was the excess acetic anhydride decomposed at the end of the reaction? (1 point)
11. What would be the test widely use to know whether I have an Aldehyde and why? (2pts) 12. What happens if I add HCl to a tertiary amine? Why? (2pts)
Please help 4 and 5. Will rate.
4. For the reaction below, draw the intermedi ate before the addition of HCle? WUCHO D HCI/10 5. What test from the Qualitative Analysis of Functional Groups would you use to determine if vanillin has been successfully reacted to form a new product in which the aldehyde group of vanillin has been oxidized?
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