Skip to main content
Chemistry LibreTexts

Extra Credit 43

  • Page ID
    83277
  • \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)

    \( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)

    \( \newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\)

    ( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\)

    \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\)

    \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\)

    \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\)

    \( \newcommand{\Span}{\mathrm{span}}\)

    \( \newcommand{\id}{\mathrm{id}}\)

    \( \newcommand{\Span}{\mathrm{span}}\)

    \( \newcommand{\kernel}{\mathrm{null}\,}\)

    \( \newcommand{\range}{\mathrm{range}\,}\)

    \( \newcommand{\RealPart}{\mathrm{Re}}\)

    \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\)

    \( \newcommand{\Argument}{\mathrm{Arg}}\)

    \( \newcommand{\norm}[1]{\| #1 \|}\)

    \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\)

    \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\AA}{\unicode[.8,0]{x212B}}\)

    \( \newcommand{\vectorA}[1]{\vec{#1}}      % arrow\)

    \( \newcommand{\vectorAt}[1]{\vec{\text{#1}}}      % arrow\)

    \( \newcommand{\vectorB}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)

    \( \newcommand{\vectorC}[1]{\textbf{#1}} \)

    \( \newcommand{\vectorD}[1]{\overrightarrow{#1}} \)

    \( \newcommand{\vectorDt}[1]{\overrightarrow{\text{#1}}} \)

    \( \newcommand{\vectE}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash{\mathbf {#1}}}} \)

    \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)

    \( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)

    Q17.6.2

    Aluminum (\(E^{o}_{Al3+/Al} = -2.07 V\)) is more easily oxidized than iron (\(E^{o}_{Fe3+/Fe} =−0.477 V\)), and yet when both are exposed to the environment, untreated aluminum has very good corrosion resistance while the corrosion resistance of untreated iron is poor. Explain this observation.

    S17.6.2

    Answer/Explanation:

    Aluminum is more easily oxidized because it has a much more negative reduction potential value than that of iron. So if so if the metals we touching and were open to the air, Zinc would act as a sacrificial anode, preventing the iron from corroding. However, when both of the elements are exposed to the air by themselves, they both corrode (there's nothing to protect them from oxidizing). Iron having less resistance to corrosion simply has to do with its chemical properties, not its electrochemical ones.

    To add on to the previous paragraph, the untreated aluminum has good corrosion resistance because it has a natural layer of aluminum oxide that protects the metal from being oxidized. The layer of aluminum oxide shield the metal from environmental elements like air and water. Since aluminum oxide never flakes off, air and water will not be able to come into contact with the aluminum metal and the metal will not corrode. (Done by Emily Tu)


    Q12.3.6

    Regular flights of supersonic aircraft in the stratosphere are of concern because such aircraft produce nitric oxide, NO, as a byproduct in the exhaust of their engines. Nitric oxide reacts with ozone, and it has been suggested that this could contribute to depletion of the ozone layer. The reaction \(NO+O_{3}\rightarrow NO_{2}+O_{2}\) is first order with respect to both NO and O3 with a rate constant of \(2.20×10^{7}\) L/mol/s. What is the instantaneous rate of disappearance of NO when \(NO=3.3×10^{−6}\) M and \([O_{3}]=5.9×10^{−7}\) M?

    S12.3.6

    Answer:

    Instantaneous Rate of Disappearance of \(NO=-4.3×10^{-5}\) M/s

    Step-by-Step Explanation:

    \[\frac{-d[NO]}{dt}=\frac{-d[O_{3}]}{dt}=\frac{d[NO_{2}]}{dt}=\frac{d[O_{2}]}{dt}\]

    The rate of disappearance of each reactant is negatively proportional to the appearance of each product. The overall rate of the reaction is equivalent to the rate of disappearance of NO times the rate of disappearance of \(O_{3}\) times the rate constant, which are all given.

    Plug the values in:

    \[Rate =(2.2×10^{7}\frac{1}{Ms})[NO][O_{3}] *\]

    \[Rate =(2.2×10^{7}\frac{1}{Ms})[3.3 10^{−6}M][5.9×10^{−7}M]\]

    And solve for the overall rate of the equation:

    \[Rate = 4.3×10^{-5}\frac{M}{s}\]

    Since the overall rate of the reaction is \(4.3 × 10^{-5}\) M/s (and equivalent to the rate of formation), the rate of disappearance is the negative equivalent of the formation rate according to the balanced equation.

    *Molarity (M) = moles/Liter


    Q12.5.15

    The hydrolysis of the sugar sucrose to the sugars glucose and fructose,

    \(C_{12}H_{22}O_{11}+H_{2}O\rightarrow C_{6}H_{12}O_{6}+C_{6}H_{12}O_{6}\)

    follows a first-order rate equation for the disappearance of sucrose: \(Rate = k[C_{12}H_{22}O_{11}]\) (The products of the reaction, glucose and fructose, have the same molecular formulas but differ in the arrangement of the atoms in their molecules.)

    1. In neutral solution, k = \(2.1 × 10^{−11} s^{−1}\) at 27 °C and \(8.5 × 10^{−11} s^{−1}\) at 37 °C. Determine the activation energy, the frequency factor, and the rate constant for this equation at 47 °C (assuming the kinetics remain consistent with the Arrhenius equation at this temperature).
    2. When a solution of sucrose with an initial concentration of 0.150 M reaches equilibrium, the concentration of sucrose is \(1.65 × 10^{−7}\) M. How long will it take the solution to reach equilibrium at 27 °C in the absence of a catalyst? Because the concentration of sucrose at equilibrium is so low, assume that the reaction is irreversible.
    3. Why does assuming that the reaction is irreversible simplify the calculation in part (b)?

    S12.5.15

    Answer:

    1. Calculations
      1. \(E_{a}\) = 108 KJ
      2. Frequency Factor (A) = \(1.4 x 10^{8}\)
      3. Rate Constant (k)= \(3.16 x 10^{-10} s^{-1}\)
    2. Time to reach equilibrium at 27 °C without a catalyst = \(6.53 x 10^{11}\) s
    3. Explanation = This simplifies the calculation because then we don't have to account for any product that concurrently becomes a reactant, or started out as a reactant, became a product, and then became a reactant again.
    Step-by-Step Explanation:
    1. Calculations \[k = Ae^{-Ea/RT}\] (Note: Temperature in Kelvin)
      1. \(E_{a}\)

        1. \(E_{a}\) is equivalent for both sets of temperature and k-values. Use the log of each and set them equal, solve for \(E_{a}\)
          1. \(ln(2.1 × 10^{−11}) = lnA - \frac{Ea}{(8.314)(300)}\)
          2. \(ln(8.5 × 10^{−11}) = lnA - \frac{Ea}{(8.314)(310)}\)
          3. Solve for A:
            1. lnA =\(ln(2.1 × 10^{−11}) - \frac{Ea}{(8.314)(300)}\)
            2. lnA =\(ln(8.5 × 10^{−11}) - \frac{Ea}{(8.314)(310)}\)
          4. Set them Equal:
            1. \(ln(2.1 × 10^{−11}) - \frac{Ea}{(8.314)(300)}\) = \(ln(8.5 × 10^{−11}) - \frac{Ea}{(8.314)(310)}\)
          5. Solve for \(E_{a}\)
            1. \(\frac{-Ea}{(8.314)(300)} + \frac{Ea}{(8.314)(310)} = ln(8.5 × 10^{−11}) - ln(2.1 × 10^{−11})\)
            2. \(E_{a}(\frac{-1}{(8.314)(300)} + \frac{1}{(8.314)(310)}) = ln(8.5 × 10^{−11}) - ln(2.1 × 10^{−11})\)
            3. \(E_{a}\) = \(\frac{ln(8.5 × 10^{−11}) - ln(2.1 × 10^{−11})}{-1/(8.314)(300) + 1/(8.314)(310)}\)
            4. \(E_{a}\) = 108103.5999 J = 108.103 KJ
      2. Frequency Factor

        1. \(2.1 × 10^{−11} = Ae^{-108103/(8.314)(300)}\)
          1. A = \(\frac{2.1 × 10^{−11}}{e^{-108103/(8.314)(300)}}\)
          2. A = \(1.4 x 10^{8}\)
        2. \(8.5 × 10^{−11} = Ae^{-108103/(8.314)(310)}\)
          1. A = \(\frac{8.5 × 10^{−11}}{e^{-108117.2/(8.314)(310)}}\)
          2. A = \(1.4 x 10^{8}\)
      3. Rate Constant (k)

        1. \(k = Ae^{\frac{-Ea}{RT}}\)
        2. k = \(1.4 x 10^{8}e^{-108103/(8.314)(47+273)}\)
        3. k = \(1.4 x 10^{8}e^{-40.633}\)
        4. k = \(3.16 x 10^{-10}\)
    2. Time to reach equilibrium at 27 °C without a catalyst

      1. This reaction is first order, so we know that \(ln(\frac{[A]}{[A]_{o}})\) = -kt and we know the initial and final concentration, and k at 27 °C
        1. \(ln(\frac{[1.65 x 10^{-7}}{[.150]}) = -2.1 × 10^{−11}t \)
        2. t = \(\frac{ln([1.65 x 10^{-7}]/[.150])}{-2.1 × 10^{−11}}\)
        3. t = \(6.53 x 10^{11}\) s = \(1.09 x 10^{10}\) min = \(1.81 x 10^{8}\) hr = \(7.56 x 10^{6}\) days = 20717.4 years

    Q21.4.10

    Predict by what mode(s) of spontaneous radioactive decay each of the following unstable isotopes might proceed:

    1. \(^{6}_{2}He\)
    2. \(^{60}_{30}Zn\)
    3. \(^{235}_{91}Pa\)
    4. \(^{241}_{93}Np\)
    5. \(^{18}_{9}F\)
    6. \(^{129}_{56}Ba\)
    7. \(^{237}_{94}Pu\)

    S21.4.10

    Answer:

    1. \(ß^{-}\) Decay \(^{0}_{-1}\textrm{e}\)
    2. \(ß^{+}\) Decay \(^{0}_{1}\textrm{e}\)
    3. \(ß^{-}\) Decay \(^{0}_{-1}\textrm{e}\)
    4. \(ß^{-}\) Decay \(^{0}_{-1}\textrm{e}\)
    5. \(ß^{+}\) Decay \(^{0}_{1}\textrm{e}\)
    6. \(ß^{+}\) Decay \(^{0}_{1}\textrm{e}\)
    7. Alpha Decay \(^{4}_{2}\textrm{He}\)
    Step-by-Step Explanation:

    Screen Shot 2017-06-05 at 4.23.46 PM.png

    1. n/p = 6/4 = 1.5>1; The approximate slope of the middle the belt of stability is about 1.5 in the upper right hand of the graph and goes closer to 1 near the origin (assuming the belt interests with the origin and has a y intersect of zero, you can approximate using y= mx+ b). While it might be hard to see, the on the graph, this assumption can be used to evaluate that this isotope lays ABOVE the belt of stability (1.5> 1), which according to the chart indicates that it has \(ß^{-}\) decay; \(^{6}He \rightarrow ^{6}Li + _{-1}e\).
    2. n/p = 30/30 = 1<1.2; Using a similar understanding, you can approximate the slope in that area of the curve and also compute the n/p ratio. This time, however, the ratio number is BELOW the approximated slope, which if you can't see from simply reading the graph, should be \(ß^{+}\) decay; \(^{60}Zn \rightarrow ^{60}Cu + _{1}e\).
    3. n/p = 144/91 = 1.55> 1.5; The first thing you should note is that Z = 91, which is greater than 83, which should indicate that it has alpha decay. However, due the large number of neutrons in relation to protons, is lands just to the left of the curve, making it \(ß^{-}\) decay. In the middle chart, it lands in the small "orange island" in the upper right hand corner.
    4. n/p = 148/93= 1.6>1.5; The first thing you should note is that Z = 93, which is greater than 83, which should indicate that it has alpha decay. However, due to the same reasoning as the previous element, it falls to the left of the belt and is thusly \(ß^{-}\) decay.
    5. n/p = 9/9 = 1<= 1ish; again, its hard to see near the origin, but at around p = 8 or 9, the slope of the belt increases, making it likely that this isotope fall beneath it, making it \(ß^{+}\) decay.
    6. n/p = 73/56 = 1.3<1.33; Since this falls really close to the belt, it is again hard to see. But approximations put the ratio just below the slope of the belt, making it \(ß^{+}\) decay.
    7. The first thing you should note is that Z = 94, which is greater than 83, which should indicate that it has alpha decay. (However, the internet indicates that Electron Capture is much more likely, but according to the material Professor Larson gave us, alpha decay is correct)

    * The notation for this problem is rather confusing. The isotope was written as Np, with an atomic number of 94 and and mass number of 241. However, the atomic number of Np is actually 93. Plutonium has an mass number of 94, in which case, the isotope would be Plutonium-241 and not Neptunium 241. Regardless, both should have a similar type of decay.


    Q20.2.14

    Copper metal readily dissolves in dilute aqueous nitric acid to form blue \(Cu^{2+}\)(aq) and nitric oxide gas.

    1. What has been oxidized? What has been reduced?
    2. Balance the chemical equation.

    S20.2.14

    Answer:

    1. Cu is Oxidized; The Nitric Acid is reduced.
    2. \(3Cu_{(s)} + 6H^{+}_{(aq)} + 2HNO_{3(aq)} \rightarrow 3Cu^{2+}_{(aq)} + 2NO_{(g)​​​​​​} + 4H_{2}O_{(l)}\)
    Step-by-Step Explanation:
    1. Which is oxidized? Which is reduced?

      1. Remember the acronym : OIL RIG (Oxidation Is Losing Reduction Is Gaining)
      2. Cu metal has no charge, but after the reaction it has a positive charge. This means it has lost electrons, and therefore is Oxidized, because oxidation is the losing of electrons.
      3. Look at the oxidation states of each elemental atom in other compounds.
        1. \(HNO_{3}\)
          1. H: +1, N: +5 , O: -2
        2. NO
          1. N: +2, O: -2
      4. The oxidation number of Nitrogen decreases, which means electrons are gained which lowers the positive charge. This means \(HNO_{3}\) is reduced, because reduction is the gaining of electrons.
    2. Balance the Chemical Equation: \(Cu_{(s)} + HNO_{3(aq)} \rightarrow Cu^{2+}_{(aq)}+ NO_{(g)​​​​​​}\)

      1. Make sure metals and non water related atoms are balanced (Basically anything besides H and O)
        1. There is one mole of Copper on each side and one mole of Nitrogen on each side
      2. Break the Reaction up in Half-Reactions:
        1. Oxidation: \(Cu_{(s)} \rightarrow Cu^{2+}_{(aq)}\)
        2. Reduction: \(HNO_{3(aq)} \rightarrow NO_{(g)​​​​​​}\)
      3. Balance Oxygen by adding \(H_{2}O\) molecules
        1. Oxidation: \(Cu_{(s)} \rightarrow Cu^{2+}_{(aq)}\)
        2. Reduction: \(HNO_{3(aq)} \rightarrow NO_{(g)​​​​​​} + 2H_{2}O_{(l)}\)
      4. Balance H by adding H+
        1. Oxidation: \(Cu_{(s)} \rightarrow Cu^{2+}_{(aq)}\)
        2. Reduction: \(3H^{+}_{(aq)} + HNO_{3(aq)} \rightarrow NO_{(g)​​​​​​} + 2H_{2}O_{(l)}\)
      5. Balance the charge by adding electrons to the opposing side
        1. Oxidation: \(Cu_{(s)} \rightarrow Cu^{2+}_{(aq)} + 2e^{-}\)
        2. Reduction: \(3e^{-} + 3H^{+}_{(aq)} + HNO_{3(aq)} \rightarrow NO_{(g)​​​​​​} + 2H_{2}O_{(l)}\)
      6. Multiply each half-reaction by a factor so that the electrons are equal
        1. Oxidation: \(3Cu_{(s)} \rightarrow 3Cu^{2+}_{(aq)} + 6e^{-}\)
        2. Reduction: \(6e^{-} + 6H^{+}_{(aq)} + 2HNO_{3(aq)} \rightarrow 2NO_{(g)​​​​​​} + 4H_{2}O_{(l)}\)
      7. Add the half-reactions and cancel terms that occur on both sides
        1. \(3Cu_{(s)} + 6H^{+}_{(aq)} + 2HNO_{3(aq)} + 6e^{-}\rightarrow 3Cu^{2+}_{(aq)} + 2NO_{(g)​​​​​​} + 4H_{2}O_{(l)} + 6e^{-}\)
      8. Answer: \(3Cu_{(s)} + 6H^{+}_{(aq)} + 2HNO_{3(aq)} \rightarrow 3Cu^{2+}_{(aq)} + 2NO_{(g)​​​​​​} + 4H_{2}O_{(l)}\)

    Q20.5.9

    Concentration cells contain the same species in solution in two different compartments. Explain what produces a voltage in a concentration cell. When does V = 0 in such a cell?

    S20.5.9

    Answer/Explanation:

    Concentration cells are composed the same species of anode and cathode, only in two different concentrations . Voltage is produced as the concentrations equilibrate. Molarity is determined by the number of dissolved ions in the aqueous environment. Electrons will flow to the species with a higher concentration, where they will bind to the aqueous ions, producing pure metal, which decreases the concentration of the ion in the solution. This continues until the concentrations are equal on both sides. When the concentrations are equal, V = 0, because there is no more electron flow.

    Note: Large concentration differences means more electron flow and spontaneity


    Q24.6.5

    How can CFT explain the color of a transition-metal complex?

    S24.6.5

    Answer/Explanation:

    Screen Shot 2017-06-07 at 9.23.23 AM.pngScreen Shot 2017-06-07 at 9.23.31 AM.png

    Crystal Field Theory's (CFT) connection to the color of transition metal complexes is rather complex. First, you have to understand that when transition metals bind to ligands, the d orbital splits into high and low energy orbitals. The difference in energy between the two levels is called ∆o (octahedral) or ∆t (tetrahedral). The larger ∆ is, the harder it is to promote electrons up to the higher energy level. The cool thing is, however, photons carry energy. So light can hit the transition complex and that energy can be used promote an electron up to that higher energy level. So transition metals absorb a certain amount of energy from light, and using ∆=hc/λ, you can calculate the wavelength (λ) of the light absorbed. All other wavelengths of light are reflected. Using knowledge of the electromagnetic spectrum and a color wheel, you can determine the color of a metal simply by what it reflects. For example, if a transition metal absorbs photons with a wavelength of 410 nm, they will appear yellow because they absorb violet light.


    Extra Credit 43 is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by LibreTexts.

    • Was this article helpful?