pract - source of error Flashcards

source of error + rectification (35 cards)

1
Q

metal + acid
volume gas collection

A

error
exothermic reaction
might raise temp, solution
rate of reaction faster than expected

improve
thermostatically controlled water bath

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2
Q

metal + acid
rate of reaction

A

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

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3
Q

record temperature change expt.

A

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

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4
Q

titration

A

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.

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5
Q

anything involving conc. of soln

A

evaporation, liquid
cover w/ petri dish

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6
Q

does chem accept (end point not definitive due to color)

A

NO

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7
Q

delay in human reaction time

A
  • starting/stopping stopwatch
  • time inaccurate
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8
Q

heating of soln,
get solid (i.e. crystallisation/loss of mass)

A

sputtering
- mass of solid lower than expected
- consider lower heat of boiler/cotton wool if loss mass

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9
Q

change of apparatus
improve expt

A

instead of measuring cylinder -> burette

water displacement to collect volume of gas -> gas syringe

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10
Q

finding heat rise
what is advantage of using graph vs using experimental method

A

graph not affected by heat loss to surrounding

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11
Q

how to do cation test on solid

A

acidify with dilute acid
only do cation test on soln.

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12
Q

disadv, pipette/burette

A

slow for liquid to move out of pipette/burette, unsure when to start stopwatch

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13
Q

disadv of using beaker vs conical flask

A

conical flask difficult swirl contents w/o spill

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14
Q

h2o2, KI source of error

A

h2o2 decomposes in room temp, pressure

KI oxidised, iodine when exposed, o2, loss, chemical

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15
Q

which salts can absorb moisture from atmosphere

A

zinc chloride, sodium hydroxide, absorb moisture, air, increase mass

and also all the gas dryers
conc. sulfuric acid
calcium oxide
(fused) calcium chloride

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16
Q

methyl orange if pH7 why kinda sucks

A

methyl orange only change color, pH3-4

17
Q

last resort source of error

A

only one stopwatch used, many different expt.

repeat 3x, find avg

18
Q

impurities in solid P
measure %tage purity by titrate P w/ HCl
error

A

impurities i.e. carbonate might react w/ acid

higher %tage purity, expected

19
Q

salt prep source of error

A
  • may not be completely dry, mass obtained high, expect
  • some solids lost, filtration
  • sputtering -> solids lost
20
Q

thermal decomposition source of error

A
  • not completely thermal decomposed, some water/carbonate content still present
  • anhydrous salt formed may absorb water, surroundings
21
Q

how to decompose hydrated CuSo4 that will decompose -> So2 gas also

A

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

22
Q

when add acid (acidify) report

A
  • any ppt
  • solubility of ppt
  • any gas
23
Q

when warm soln. with test tube what other precautions to take

A
  • use boiling tube, larger cap, better control, small quantity soln may spurt out quickly, heating
  • remove tube from flame time to time, prevent spurt
  • apply heat w/ gentle/small flame
24
Q

deposit vs solid vs residue

A

deposit: metal
solid: colour change when heat
residue: phys separate

25
soln vs suspension aka is there ppt or not.
soln: swirl, leave to stand, no solid particles, light can pass thru
26
chromatography expt. full
- fill test tube, 2cm depth water - start line, chromatography paper, pencil, add spot - chromatography paper -> test tube - ensure solvent below start line - split cork, chromatography paper in place - wait 10min - take out chromato paper, mark solvent front immediately - spray locating agent, separate, x no of dots - measure distance from SL -> Solvent, measure distance from SL -> Spot - calculate Rf value, compare against known values, amino acids
27
explain y water added each reaction mixture
keep total vol reaction mix constant
28
why heating more NaHCo3 decompose further
compose further into Na2O and co2
29
differentitate calcium carbonate and zinc carbonate
heat strongly, zinc carbonate will decompose
30
record highest and lowest temp of exothermic reaction how to improve accuracy
draw graph - derive temperature rise from extrapolated reading - measure highest temp will have heat loss
31
improve accuracy
- light sensory/colorimeter w/ data logger for reaction time - glass rod stir instead of thermometer - temperature sensor connect to data logger - cool test tube and its contents in a dessicator, use larger mass of solid when decomposing - heat until constant mass observed, collect co2 and record vol o fgas, no further change
32
QA format
add few drops... add in excess..
33
generic sources of error
- only one stopwatch used for multiple samples - same size dosent mean same mass
34
porous pot diagram
https://docs.google.com/document/d/1Ep_FO9CxYSFbxmf3Zqg9mgm9NNyt2enpfMDr49gufrU/edit?tab=t.0 page 42
35
when use large pieces of metal + acid what is disadv
dosent allow for fast reaction max heat recorded may be lower than usual