topic eleven Flashcards

1
Q

qualitative data

A

includes non-numerical data obtained from observations that are made during an experiment, not from actual measurements.

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2
Q

quantative data

A

includes numerical data (numbers), such as measurements taken in the laboratory during an experiment. Examples include mass, volume, temperature, voltage, pH, density and absorbance. Remember that when recording a measurement, there is an experimental error or degree of random uncertainty associated with the value.

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3
Q

SI units for electric current

A

amperes, A

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4
Q

Si units for temperature

A

kelvin, K

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5
Q

SI units frequency

A

hertz (reciprocal of seconds) Hz (s-1)

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6
Q

SI units pressure

A

newtons per square metre Pa (Nm-2)

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7
Q

examples of random errors

A

a breeze through an open door, which affects the mass measured on a mass balance

changes in the temperature of a room between morning and afternoon

errors of judgement when reading a scale on a measuring instrument.

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8
Q

random erros cannot be eliminated completely, but they can be reduced by

A

conducting repeat trials and taking an average of to the results

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9
Q

how to report measured quantities with a range of uncertainty

A

When taking a reading from analogue equipment (such as a measuring cylinder), you can estimate the value to within half of the smallest scale division. In the case of the measuring cylinder shown in Figure 1, the smallest scale division is 1 cm3, so half of the smallest division is 0.5 cm3.

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10
Q

systematic errors are caused by

A

a piece of apparatus has been wrongly calibrated

a scale is consistently misread by the experimenter

the apparatus is faulty.

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11
Q

examples of systematic errors include

A

not zeroing a mass balance before use (a non-zero error)

heat loss during an experiment to measure an enthalpy change

a leak in the apparatus used to measure a volume of gas.

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12
Q

parallax error

A

when a scale or measuring cylinder is read from the wrong position

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13
Q

systematic errors in determining enthalpay change

A

A significant proportion of the heat released by burning the alcohol is lost to the surroundings.

Heat is lost from the water and absorbed by the calorimeter itself.

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14
Q

random errors when determining enthalpy change

A

Random uncertainties when recording the masses of the alcohol and the water.

Random uncertainties when recording the temperature of the water during the experiment.

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15
Q

precision refers to

A

how close several experimental measurements or values are to each other

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16
Q

accuracy refers to

A

how close the readings or values are to the actual value

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17
Q

absolute uncertainity

A

The degree of uncertainty in a measurement is usually expressed in the same units as the measurement itself. This is the absolute uncertainty of the measurement, for example, 28.5 ± 0.1 °C

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18
Q

in order to calculate the total uncertainty

A

the absolute uncertainties can either be added together or converted to percentage uncertainties, which are then added together.

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19
Q

The equation used to calculate the percentage uncertainty is shown below:

A

Percentage uncertainty =
absolute uncertainty/measured value×100%

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20
Q

percentage error equation

A

Percentage error = (experimental value - theoretical value) / theoretical value × 100%

21
Q

when plotting experimental data, the ind and dep variable goes on which axis

A

the independent variable is plotted on the x-axis and the dependent variable is plotted on the y-axis

22
Q

When plotting a graph:

A

plot the independent variable on the x-axis and the dependent variable on the y-axis

label the axes and ensure your labels include the correct units

choose an appropriate scale for each axis

give your graph an appropriate title

draw a line of best fit (see below).

23
Q

line of best fit

A

the line will not necessarily pass through all of the points; instead, you should try to ensure that approximately half the data points lie above the line, and half lie below. Outliers (points that do not seem to fit the overall trend) are not included in the data used to draw the line of best fit.

24
Q

gradient at a particular point on a curve

A

interpolation, draw a tangent to the curve at that point and find the gradient of the tangent using the relationship, m=change in y / change in x

25
Q

extrapolation on a graph

A

drawing the line further than where it goes
to find a data point outside the range of measured values.

26
Q

ihd formula

A

IHD=(2x + 2 - y)/2

27
Q

whicha toms dont affect the IHD

A

oxygen and sulfur

28
Q

what are halogen atoms treated as in ihd

A

hydrogen atoms

29
Q

what to do with nitrogen atoms in ihd

A

add one carbon and one hydrogen

30
Q

what is IR spectroscopy used for

A

to identify the bonds present within a molecule

31
Q

how is IR radiation use din IR spec

A

it is absorbed by certain types of bond and causes them to stretch or bend which can then be used to gain info about the type of bonds within the molecule

32
Q

Gases that absorb IR radiation are known as being

A

IR active

33
Q

amount of IR absorbed relies on

A

The amount of IR radiation absorbed by a bond depends on its polarity - strongly polar bonds absorb more and weakly polar bonds absorb less. Non-polar bonds such as C-C, for example, usually do not absorb IR radiation and do not show up on an IR spectrum.

34
Q

can divide IR into

A

functional group and fingerprint region

35
Q

wavenumber is equal to

A

the number of wavelengths per centimetre

36
Q

what do peaks correspond to

A

the amount of IR radiation absorbed by the bodns in the compound

37
Q

what is ionisation

A

where the sample in question is bombarded by high-energy electrons

38
Q

The collisions that take place in a mass spectrometer are so energetic that they cause the molecules to break up into different

A

fragments

39
Q

The fragmentation pattern produced in a mass spectrometer gives evidence about the

A

structure of the compound

40
Q

what can proton nmr identify

A

the different chemical environments in a molecule that contain hydrogen atoms (or protons).

41
Q

a higher-energy spin state (–½), when the nuclei line up with

A

their magnetic fields against the external magnetic field

42
Q

a lower-energy spin state (+½), when the nuclei line up with

A

their magnetic fields in the same direction as the external magnetic field.

43
Q

number of peaks in nmr gives

A

number of different chemical environments in which hydrogen atoms or protons are located

44
Q

in nmr, The position on the x-axis where a peak occurs is known as its

A

chemical shift, measured in ppm

45
Q

The chemical shift of each signal is measured relative to the peak produced by

A

tetramethylsilane (TMS)

46
Q

protons in the same chemical environment are known as

A

equivalen tprotons

47
Q

integrated trace

A

the height of each step is proportional to the number of protons in that chemical environment

48
Q
A