Exam Study: practice Flashcards
List four types of information that can be found in a compounds material safety data sheet
Flammability
Chemical identification
Health hazards
Reactivity data
Physical data
First aid info
test
What WWU document contains information pertaining to emergency procedures, storage and handling of hazardous materials, proper disposal of hazardous materials (waste), laboratory clothing policy, and methods of training workers?
CHEMICAL HYGEINE PLAN
Lab coats, safety goggles and gloves are collectively known as PPE. What does PPE stand for?
Personal Protective Equipment
Write the proper name for each piece of equipment labeled in the distillation
apparatus pictured below.
Starting top left, going clockwise:
Claisen adapter
Distillation head
Water condenser
Vacuum take-off adapter
Graduated cylinder
Distilling flask / round-bottom flask
In which of the following solvents will 4-methylbenzoic acid have the highest solubility?
Dichloromethane
Ethanol
Toluene
Ethanol
Polar, h-bond donor AND acceptor.
Rank the following solvents with respect to polarity (1 being most polar):
Toluene
Hexane
Ethyl acetate
Ethyl ether
Acetone
1 - Acetone
2 - Ethyl acetate
3 - Ethyl ether
4 - Toluene
5 - Hexane
Give two reasons why acetone is a good solvent to use for rinsing out glassware as part of the cleaning process
- It has a low boiling point and therefore evaporates easily
- Its electronegative oxygen atom creates a polarity, so acetone easily attracts many compounds
- It’s miscible with water
How do you repurify sulfanilamide if it has been dropped on the floor?
- Recrystallization: dissolve in boiling ethanol, cool, and do vacuum filtration
- Column chromatography
How do you find % recovery?
% yield / theoretical yield
Is a sulfanilamide sample 161.6-163.2C pure if MP = 165-165C?
No - The range is narrow - melting range is broadened if sample is impure
Lowered range likely due to uncalibrated apparatus
How do you calculate Rf?
Distance traveled / solvent front
Remember sig figs!
Are more or less polar solvents closer to solvent front?
Less, they’re less held back by stationary phase
What (e.g. polarity) elutes first in column chromatography?
Least polar
List in order of polarity: alcohols, cabonyls, alkenes
alkenes < carbonyls < alcohols
How does solvent polarity affect compound location in TLC?
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