Slides exam 1 Flashcards

1
Q

What is the definition of analytical chemistry?

A

Analytical chemistry is the science of obtaining, processing, and communicating information about the composition and structure of matter.

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2
Q

List the steps of chemical analysis

A
  • Formulating the Question
  • Selecting Analytical Procedures
  • Sampling
  • Sample Preparation
  • Analysis of Sample
  • Interpretation of Results
  • Drawing Conclusions
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3
Q

Define significant figures

A

The minimum number of digits required to express a value in scientific notation without loss of accuracy

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4
Q

List an example of a) reproducible/systematic error and b) irreducible/random error

A

a) instrument calibration causes 0.01unit difference b) noise causes random difference in measurement

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5
Q

What % of data in a gaussian distribution lies within 1, 2 and 3 standard deviations of the mean?

A

68.3, 95.5, 99.7

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6
Q

What is the difference between linear range, dynamic range, and range?

A

Linear range: instrument response is proportional to concentration.

Dynamic range: instrument response is detectable (different) for each concentration, even if it’s not linear.

Range: entire spread of data.

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7
Q

What is the matrix effect?

A

A change in analyte signal caused by anything other than analyte.

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8
Q

What is Le Chatelier’s Principle?

A

Any change in a system not at equilibrium is such that it moves towards equilibrium.

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9
Q

What is a Bronsted-Lowry acid-base pair?

A

An acid (contains an ionizable H) and its conjugate base (the anion when H is lost)

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10
Q

What is a buffer? What is buffer capacity?

A

A buffer is a solution that resists changes in pH when an acid or a base is added to it. Buffers typically consist of a weak acid and its conjugate base (or a weak base and its conjugate acid) in solution.

A measure of how well the solution resists changes in pH when a strong acid or base is added

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11
Q

(2) A student creates a calibration curve of the concentration of calcium in water using titration and FAAS. They measure 5 total samples then calculate a t value of 2.500. The students t-table value for a 95% confidence interval is 2.776. Do they reject or fail to reject the null hypothesis? Why?

A

Fail to reject – tcalc < ttable, so the null hypothesis (that the 2 sets of measurements are not different) can’t be rejected

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12
Q

(2) Explain how to construct a representative sample from a) homogenous/random heterogenous material and b) segregated heterogenous material

A

a) divide into segments and collect random portions (called random sample)

b) divide into segments & collect a number of portions from each section in the ratio that they comprise the total sample (ex. 25% of samples come from the
material that makes up 25% of the total material) (called composite sample)

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13
Q

(2) You collect measurements of 4.5, 9.2, 1.4, 5.6, and 8.0 and perform a q-test. Should 1.4 be discarded? Explain.

A

Q = 0.40. 0.40 < 0.64. Don’t discard 1.4.

If Q > Qtable, where Qtable is a reference value corresponding to the sample size and confidence level, then reject the questionable point.

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14
Q

(2) Explain the difference and list a way to verify a) precision and b) accuracy

A

a) perform many repeats & look at st. dev.

b) compare to SRM

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15
Q

(2) Lisa creates a calibration curve with [x] 2.0, 3.0, 4.5, 6.0 and 7.0 M. She measures her unknown and calculates [x] = 1.5 based on her calibration curve. Can she rely on this concentration?

A

No – she extrapolated beyond the curve. (She could solve by running another standard of 1.0 M to see if this value is within the linear range.)

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16
Q

(2) A student creates a program to make calibration curves using the method of least squares. The program minimizes the sum of the square of the difference in x values. Is this approach correct? Why or why not?

A

This is incorrect – x-values represent standards, so x-errors are much smaller than y-errors. The method of least squares aims to minimize the sum of the square of y differences.

17
Q

(2) Based on the quality control chart, if 0.5% of your data is outside the action lines, and 6.7% is outside the warning lines, what should you do? Why?

A

They should use a new method. Only 0.3% of data should be outside the action lines, and 4.5% of data should be outside the warning lines.

18
Q

(2) You measure the content of riboflavin in beer using HPLC but cannot distinguish the riboflavin peak. How can you solve this issue to create a calibration curve?

A

Add riboflavin standard to your sample in increments and measure the response.

19
Q

(2) Why could a sample below the detection limit give a negative instrument response?

A

Below the detection limit your sample is not significantly different from the blank so you’re just measuring noise.

20
Q

(2) What is suggested by a large K value and why?

A

A large K means the reaction heavily favors the products at equilibrium because K = [P]/[R].

21
Q

(2) Why do you need to know the Keq to find the concentration of a weak acid’s constituents, but not a strong acid?

A

Strong acids dissociate completely, so [A] and [H] are equal to initial [HA].

22
Q

(2) What is the predominant form of acetic acid (pKa = 4.76) at pH = 5?

A

Acetate anion – pH > pKa, meaning there are few enough H+ ions in solution that the acid will dissociate

23
Q

(3, 1) What is the correct answer with the correct number of sig figs: (1.290 x 10E3) + 70,001 – (9.742 x 10E2)

A

70,317

24
Q

(3, 3) Analysis of your unknown tells you it contains 5.00 µM quercetin. You spike it with 15.0 µM quercetin, and your instrument reads a signal corresponding to 18.6 µM quercetin. What is the % spike recovery?

A

100*[(18.6-5)/15] = 90.7%