chembio finals lec Flashcards

(59 cards)

1
Q

a measure of how close a measurement is to the true or (standard) value of the quantity being measured.

A

accuracy

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2
Q

measure of how close a series of measurements are to one another.

A

precision

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3
Q

agreement or closeness among measured values between runs.

A

reproducibility

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4
Q

agreement or closeness among measured values within runs.

A

repeatability

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5
Q

two components of precision

A

reproducibility and repeatability

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6
Q

amount of error in your measurements. difference between the measured value and “true” value.

A

absolute error

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7
Q

ratio of absolute error and the true (standard) value

A

relative error

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8
Q

ways of expressing accuracy

A

absolute error (AE) and relative error (RE)

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9
Q

average of different variations from a data set.

A

average deviation

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10
Q

denoted by 𝜎 or s

A

standard deviation

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11
Q

denoted by 𝜎 or s

A

variance

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12
Q

a measurement of the spread between numbers in a data set

A

variance

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13
Q

also known as the Relative Standard Deviation (RSD)

A

coeffecient variation

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14
Q

the ratio of the standard deviation and the mean.

A

coeffecient variation

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15
Q

difference between the lowest and highest values.

A

range

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16
Q

ways of expressing precision

A

average deviation
standard deviation
variance
coefficient variation
range

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17
Q

lowers the accuracy of the experiment.

A

error in measurements

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18
Q

types of error

A

determinate/systematic error
indeterminate/random error
propagation of error/uncertainty

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19
Q

errors that are known and controllable errors

A

determinate/systematic error

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20
Q

nonrandom error that can be detected and corrected.

A

determinate/systematic error

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21
Q

examples of determinate error

A

personal/operative, instrumental, and method errors

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22
Q

faulty or uncalibrated equipment

A

intstrumental error (determinate)

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23
Q

mathematical errors in calculations, prejudice in estimating measurements, incomplete drying, transfer solutions

A

personal/operative error (determinate)

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24
Q

most serious error ex. Coprecipitation of impurities, slight solubility of the precipitate, incomplete reactions

A

method error (determinate)

25
caused by uncontrollable or unknown fluctuations in variables that may affect experimental results.
indeterminate/random error
26
arise from uncertainties in measurements
indeterminate/random error
27
variation in line voltage, fluctuation of electrical current
instrumental error (indeterminate)
28
misestimation of the meniscus, subjectivity in color changes
personal/operative error (indeterminate)
29
variation in environmental conditions such as humidity, temperature, etc. during measurement and analysis.
method error (indeterminate)
30
result due to several deviations of the instruments used in the conduct of measurement and analysis.
propagation of error/uncertainty
31
defined as the effects on a function by a variable's uncertainty.
propagation of error/uncertainty
32
also known as confidence interval
confidence limit
33
shows how accurate an estimation of the mean is or is likely to be.
confidence limit
34
range where the true (standard) value lies
confidence limit
35
is an observation that lies an abnormal distance from other values in a random sample from a population.
outlier
36
used to identify an outlier within a data set
q-test
37
used to a determinate error; otherwise, it falls within the expected random error and should be retained
q-test
38
suspected outlier is retained
qcalc < qtab
39
suspected outlier is rejected
qcalc > qtab
40
a standard solution is added to a solution of an analyte until the reaction between the analyte and reagent is judged to be complete
titration
41
performed slowly by adding a standard solution from a buret or other liquid-dispensing device to a solution of the analyte until the reaction between the two is complete.
titration
42
solution of accurately known concentration is added gradually to another solution of unknown concentration, until the chemical reaction between the two solutions is complete
standard solution
43
the point in a titration which the amount of added standard reagents is exactly equivalent to the amount of analyte.
equivalence point
44
point in a titration when a physical change occurs that is associated with the condition of chemical equivalence.
end point
45
added to analyte solution to produce an observable physical change (the end point) at or near the equivalence point
indicators
46
a highly purified compound that serves as a reference material in volumetric method.
primary standards
47
compound whose purity has been established by chemical analysis and that serves as the reference material for a titrimetric method of analysis.
secondary standards
48
a carefully weighed quantity of a primary standard is dissolved in a suitable solvent and diluted to an exactly known volume in a volumetric flask
direct method
49
the titrant to be standardized is used to titrate a weighed quantity of a primary standard
standardization
50
these substances react more completely with an analyte than do their weaker counterparts, and they therefore provide sharper endpoints.
standard solutions
51
are prepared by diluting concentrated hydrochloric, perchloric or sulfuric acid.
standard solutions of acids
52
seldom used because its oxidizing properties offer the undesirable side reactions.
nitric acid
53
potent oxidizing agents and are very hazardous.
hot concentrated perchloric acid and sulfuric acids
54
prepared from solid sodium, potassium, and occasionally barium hydroxides.
standard solutions of bases
55
a weak organic acid or a weak organic base whose undissociated form differs in color from its conjugate base or its conjugate acid form.
acid/base indicator
56
pH range of phenolphthalein
8-10, colorless (acid), red (base)
57
compute the concentration of the acid from its starting concentration and the amount of base added
pre-equivalence
58
the hydronium and hydroxide ions are present in equal concentrations, and the hydronium ion concentration is derived directly from the ion-product constant for water.
equivalence
59
the analytical concentration of the excess base is computed, and the hydroxide ion concentration is assumed to be equal to or a multiple of the analytical concentration.
post-equivalence