metal + acid
volume gas collection
error
exothermic reaction
might raise temp, solution
rate of reaction faster than expected
improve
thermostatically controlled water bath
metal + acid
rate of reaction
error
mass, metal ribbon different
even if same length
lighter mass, lesser no. of metal particles
improve
weigh each piece before use
error
metal ribbon floats on surface, not submerged, acid, difficult completely surround, acid
improve
use glass rod, completely submerge metal strip
record temperature change expt.
error
heat produced, lost to surrounding
highest temperature measured, lower than expect
improve
place beaker, styrofoam cup (insulator, heat)
cover styrofoam cup
minimise heat lost, surrounding
titration
error
difficulty reading mensicus (liquid i.e. potassium manganate (VII)), dark liquid
inaccurate reading
solution
reading, using top of meniscus, take multiple readings, use avg
error
burette (solution i.e. acid/alkali) impure, volune of (solution in burette) needed larger than expcted, neutralise
soln. flow out of pipette slowly, dk when to start stopwatch, inaccurate time readings
only blame burette soln.
anything involving conc. of soln
evaporation, liquid
cover w/ petri dish
does chem accept (end point not definitive due to color)
NO
delay in human reaction time
heating of soln,
get solid (i.e. crystallisation/loss of mass)
sputtering
- mass of solid lower than expected
- consider lower heat of boiler/cotton wool if loss mass
change of apparatus
improve expt
instead of measuring cylinder -> burette
water displacement to collect volume of gas -> gas syringe
finding heat rise
what is advantage of using graph vs using experimental method
graph not affected by heat loss to surrounding
how to do cation test on solid
acidify with dilute acid
only do cation test on soln.
disadv, pipette/burette
slow for liquid to move out of pipette/burette, unsure when to start stopwatch
disadv of using beaker vs conical flask
conical flask difficult swirl contents w/o spill
h2o2, KI source of error
h2o2 decomposes in room temp, pressure
KI oxidised, iodine when exposed, o2, loss, chemical
which salts can absorb moisture from atmosphere
zinc chloride, sodium hydroxide, absorb moisture, air, increase mass
and also all the gas dryers
conc. sulfuric acid
calcium oxide
(fused) calcium chloride
methyl orange if pH7 why kinda sucks
methyl orange only change color, pH3-4
last resort source of error
only one stopwatch used, many different expt.
repeat 3x, find avg
impurities in solid P
measure %tage purity by titrate P w/ HCl
error
impurities i.e. carbonate might react w/ acid
higher %tage purity, expected
salt prep source of error
thermal decomposition source of error
how to decompose hydrated CuSo4 that will decompose -> So2 gas also
weigh
heat gently
heat rim of mouth when condensation forms
let it cool, notice color changes
when cooled, heat gently again and see if there is further change in mass
There will be greater loss of mass in CuSo4.xh2o as sulfate will decompose as well as hydration
HEAT GENTLY -> remove water
HEAT STRONGLY -> decompose solid TEST GAS when solid melts
when add acid (acidify) report
when warm soln. with test tube what other precautions to take
deposit vs solid vs residue
deposit: metal
solid: colour change when heat
residue: phys separate