organic analysis Flashcards
(45 cards)
What can be used to distinguish between primary, secondary, and tertiary alcohols?
Acidified potassium dichromate (K,Cr,°7)
It is a mild oxidizing agent that helps identify alcohol types through oxidation reactions.
What happens to primary and secondary alcohols when oxidized by acidified potassium dichromate?
They are oxidized and the dichromate turns from orange to green
The orange color indicates the presence of Cr2O7^2- ions, which change to Cr3+ ions.
What is the oxidation behavior of tertiary alcohols with acidified potassium dichromate?
Tertiary alcohols cannot be oxidized using dichromate
This differentiates them from primary and secondary alcohols.
What is the problem when testing primary and secondary alcohols with dichromate?
Both give the same color change
This necessitates further testing to distinguish between the products.
What method is used to collect products produced upon oxidation of primary and secondary alcohols?
Fractional distillation
This method separates components based on boiling points.
What is produced from the oxidation of primary alcohols?
Aldehyde
Aldehydes are characterized by the functional group -CHO.
What is produced from the oxidation of secondary alcohols?
Ketone
Ketones are characterized by the functional group >C=O.
What solution can be used to distinguish between aldehydes and ketones?
Fehling’s solution
Fehling’s solution is also known as Benedict’s solution.
What type of agent is Fehling’s solution?
Oxidising agent
What happens to Fehling’s solution when it reacts with aldehydes?
Goes from blue solution to brick red precipitate (Cu2O)
What happens to Fehling’s solution when it reacts with ketones?
Remains blue
What color is Fehling’s solution before the reaction?
Blue
What is the precipitate formed when aldehydes react with Fehling’s solution?
Brick red precipitate (Cu2O)
True or False: Ketones can be oxidized by Fehling’s solution.
False
Fill in the blank: Fehling’s solution is used in a _______ water bath during testing.
Hot
What reagent is used to distinguish between aldehydes and ketones?
Tollens’ reagent
Tollens’ reagent can be prepared and then used for this purpose.
What is the composition of Tollens’ reagent?
[Ag(NH3)2]+
This complex is used to test for the presence of aldehydes.
What happens when Tollens’ reagent is added to an aldehyde?
Silver reduces to form a silver coating inside the flask
This indicates a positive test for aldehydes.
What is the result of adding Tollens’ reagent to a ketone?
No silver precipitate forms
This indicates a negative test for ketones.
What is the initial appearance of silver nitrate solution?
Colourless
This is the state of the solution before any reaction occurs.
What precipitate forms when NaOH is added to silver nitrate solution?
Pale brown precipitate
This is an intermediate step in the testing process.
What must be added to the pale brown precipitate to dissolve it?
Dilute ammonia
This step is crucial for completing the test.
What safety precaution is mentioned regarding the heating of aldehydes and ketones?
Do not use a Bunsen flame
Aldehydes and ketones are flammable substances.
What is the procedure for testing an aldehyde or ketone with Tollens’ reagent?
Add the aldehyde or ketone to Tollens’ reagent and place in a hot water bath
This method ensures controlled heating.