Lab Exam 1 Flashcards
Do impurities lower or raise the melting point of a solid?
Lowers melting point
What are the apparatus needed to test melt in point of a solid?
Solid organic compound, thin walled capillary tubes, paraffin oil, laboratory thermometer, heating medium/hot plate, magnetic stirrer, 500ml beaker, retort stand and rubber band
What is paraffin oil used for when investigating melting point?
Rub it on the bulb of the thermometer before being attached to capillary tube
What are the apparatus for preparing AND purifying ethyl acetate/ ethyl ethanoate?
Chemicals: Acetic acid, 17.4M(glacial) Ethanol Concentrated sulfric acid(18M) Equipment: 2 Erlenmyer flasks/conical flasks, 125mL Boiling stones or glass beads Condenser Distilling flask Beaker 400mL for water bath Bunsen burner, ring and wire gauze Measuring cylinder Capillary dropper
Give the procedure for preparing ethyl acetate
- Place 10mL of ethanol, 12mL glacial acetic acid and 15 drops of concentrated sulfric acid and a boiling stone in an Erlenmeyer flask
- Clamp the condenser in a vertical position with the bottom inside the conical flask. This allows the condenser to act as a reflux condenser allowing mixture vapors to return to the mixture
- Slowly run cold water through the condenser, in the bottom and out of the top while heating the flask in a water bath
- Raise the temperature of the hot water until the mixture in the Erlenmeyer flask is gently boiling and continue for 15 mins
- Cool the mixture
What is the procedure for distillation of ethyl acetate?
- Pour the mixture of ethyl acetate(and boiling stone) into a distilling flask and connect the condenser to the side arm of the flask
- Insert thermometer
- Heat the bottom of the distilling flask in a hot water bath until no more distillate is coming over
- Record the temperature at which the distillation begins and the temperatures during and at the end of distillation
In preparation of ethyl acetate, why is the condenser clamped in a vertical position with the bottom inside the flask?
It acts as a reflux condenser , allowing vapors of the mixture to condense and return to the reaction vessel
What are precautions when investigating reactions between alcohols and phenols?
- Sodium dichromate is a toxic compound, so plastic gloves were used
- H2SO4 and HCl are very corrosive so there were
- Standard lab precautions used
What are precautions to be considered when finding the melting points of solids?
- Use dry and powdered sample for melting point determination
- Packing of the powder should be uniform without any big air gaps between the solid particles
- The capillary tube should be filled one fifth of its length
- Maintain uniform temperature of the liquid bath
- The rate of heating should be controlled and should be very slow near the melting point so that the melting point is recorded accurately
In testing the reactivity of alcohols and phenols, what is the method for esterification?
Add 1cm3 of glacial ethanoic acid, a few drops to concentrated sulfric acid to 2cm3 of the alcohol
Heat the mixture in a water bath
Pour the resulting mixture into water and note the smell
In testing reactivity of alcohols and phenols, write the method for oxidation
Add 2mL of 1% sodium dichromate and 5 drops of concentrated sulfric acid to each of the solutions and mix the contents thoroughly. Add 10 drops of each of the newly formed solutions to test tubes.
Cork all tubes and warm gently at 40-50 degrees Celsius in a water bath for 1 minute. Note any changes
Describe the triiodoform test
Add 5 drops of ethanol to 5 cm3 of iodine. Add NaOH until the iodine color has discharged and warm the mixture in a water bath for 2-3 minutes( temperature less than 60 degrees Celsius) cool the tube and note the crystals formed.
List three qualitative tests for alcohols
Jones oxidative test
Lucas test
Triiodoform test
Describe all possible results for the Lucas test
Primary alcohol- reacts slowly or not at all
Secondary alcohol- reacts in 1-5 minutes
Tertiary alcohol- reacts in less than a minute
What are the requirements for the iodoform test to be positive?
C attached to the -OH must also be bonded to a methyl group and hydrogen