unit 5 practical Flashcards
what are some common mistakes when making a standard solution?
- not weighing by difference
- not ensuring all your solid is dissolved before transferring to the flask
- forgetting to rinse your stirring rod/breaker/funnel
- not putting the washings into the volumetric flask
- filling the volumetric flask over the line
- failure to fully mix the solution (not inverting the flask enough times)
what are tips to look out for when making a standard solution?
- write down all the possible numbers from your weighing in rough
- keep your weighing boat on your desk and dont let anyone touch ut
- only use 100cm^3 of water to dissolve your solid initially
- use a pasteur pipette to add the last few drops of water to your volumetric
- remember the miniscus should sit on the line
- put your palm over the flask’s lid when mixing to ensure you dont lose and solution
what are some common mistakes when doing a titration?
- not conditioning your equipment with the correct solutions
- not eliminating bubbles from the burette
- filling the burette over your head
- not reading the burette at eye level
- titrating with the funnel in
- using your rough as an actual result
what are tips to look out for when doing a titration?
- practice using your burette to let out one drop at a time when you are conditioning
- balance any equations before you start so that you’re ready to do your calculation as soon as you have your result
- check you know what the end point will look like before you start titrating
- add half drops near the endpoint
- complete your rough very quickly so that you’re ready can spend more time on your ‘real’ titrations
what are some common mistakes when doing double titration?
- make sure you add the indicators in the right order - phenolphthalein is always first
what are tips to look out for when doing double titration?
- double check the equations when doing your calculations
what are some common mistakes when doing back titration?
- don’t forget its alkali in the burette, be especially careful to wear your goggles
- remember the colour changes will be the opposite to usual
what are tips to look out for when doing back titration?
- if you only take a portion of your original reaction don’t forget to factor this into your calculation
what are some common mistakes when doing redox titrations?
- forgetting to add acid if required
what are tips to look out for when doing redox titrations?
- add water from a kettle if your titration has to be carried out hot
what are some common mistakes when doing inorganic tests (precipitation reactions) ?
- failing to label all your test tubes at the start
- giving answers as ‘yes’ instead of stating what the observations are
what are tips to look out for when doing inorganic tests (precipitation reactions)?
- work out which reactions will give precipitates before you start
- remember some substances are ‘sparingly soluble’ so may be inconclusive - it is fine to record this
what are some common mistakes when doing gravimetric analysis?
- failing to test the filtrate with reagent to see if all the solid has precipitated
- forgetting to rinse the beaker into the filter paper
what are tips to look out for when doing gravimetric analysis?
- you may have to repeat the precipitation several times but make sure all your solid ends up in the same filter paper (you can add a a second piece of filter paper under the first if needed)
what are some common mistakes when measuring rate?
- taking too long, this allows the room temperature to change and will affect your results
- not measuring concentrations / volumes exactly
- writing down the tenths and hundredths of seconds from your stopwatch - dont do this
what are tips to look out for when measuring rate?
- plot your graph for rate as you go along, this way you can immediately repeat any experiments you need to - your points should be really close to your line of best fit
what are some common mistakes when using electrochemical cells?
- forgetting to soak your salt bridge
- putting the cells the wrong way round
what are some common mistakes when doing melting point experiments?
-forgetting to seal the base of the tube
what are some common mistakes when doing recrystallisation?
- using too much solvent
- putting into an ice-bath too quickly (you will only make tiny crystals)
what are tips to look out for when doing recrystallisation?
- if you cant see any crystals forming, scratch the bottom of the glass with a stirring rod. alternatively, seed the crystals by dipping a glass stir rod in the hot solution. let the solvent dry, then dip the stir rod back into the cooled solution
- make sure the solution is fully cool before filtering
what are some common mistakes when doing esterification?
- forgetting to add the concentrated acid
- forgetting to distil off the ester
what are tips to look out for when doing esterification?
- use the acid anhydride for a larger yield
what are some common mistakes when doing thermochemistry?
- taking the thermometer out to read the temperature
- forgetting to use a lid
- not taking enough readings before and after adding the reagent
what are some common mistakes when doing organic synthesis?
- not refluxing for long enough